Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84803 |
|---|---|
| ensemblid | ENSG00000138678.11 |
| hgncid | 28157 |
| symbol | GPAT3 |
| name | glycerol-3-phosphate acyltransferase 3 |
| refseq_nuc | NM_032717.5 |
| refseq_prot | NP_116106.2 |
| ensembl_nuc | ENST00000264409.5 |
| ensembl_prot | ENSP00000264409.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 83536108 |
| end | 83605875 |
| strand | + |
| ver | v1.2 |
| region | chr4:83536108-83605875 |
| region5000 | chr4:83531108-83610875 |
| regionname0 | GPAT3_chr4_83536108_83605875 |
| regionname5000 | GPAT3_chr4_83531108_83610875 |
| 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 | 434 | 327 | 92 | 45 | 140 | 11 | 37 | 116 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0002 | 0/0 | 434 | 5 | 0 | 3 | 0 | 1 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0003 | 0/0 | 434 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1305 | 326 | 91 | 45 | 140 | 11 | 37 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| c0002 | 0/0 | 1305 | 5 | 0 | 3 | 0 | 1 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| c0003 | 0/0 | 1305 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| c0004 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| 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 | 1624 | 107 | 14 | 15 | 60 | 2 | 14 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0002 | 0/0 | 1624 | 97 | 29 | 12 | 46 | 4 | 6 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0003 | 0/0 | 1624 | 75 | 5 | 18 | 30 | 5 | 17 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0004 | 0/0 | 1624 | 19 | 16 | 3 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0005 | 0/0 | 1624 | 17 | 16 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0006 | 0/0 | 1624 | 4 | 4 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0007 | 0/0 | 1624 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0008 | 0/0 | 1621 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0009 | 0/0 | 1624 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0010 | 0/0 | 1624 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0011 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0012 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0013 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0014 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| t0015 | 0/0 | 1624 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1305 | 326 | 91 | 45 | 140 | 11 | 37 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0004 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0002c0002 | 0/0 | 1305 | 5 | 0 | 3 | 0 | 1 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0003c0003 | 0/0 | 1305 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2928 | 107 | 14 | 15 | 60 | 2 | 14 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0002 | 0/0 | 2928 | 95 | 29 | 10 | 46 | 4 | 6 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0003 | 0/0 | 2928 | 70 | 5 | 15 | 30 | 4 | 16 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0004 | 0/0 | 2928 | 18 | 15 | 3 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0005 | 0/0 | 2928 | 17 | 16 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0006 | 0/0 | 2928 | 4 | 4 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0007 | 0/0 | 2928 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0008 | 0/0 | 2925 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0009 | 0/0 | 2928 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0010 | 0/0 | 2928 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0011 | 0/0 | 2927 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0012 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0013 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0014 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0001t0015 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0001c0004t0004 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0002c0002t0003 | 0/0 | 2928 | 5 | 0 | 3 | 0 | 1 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| a0003c0003t0002 | 0/0 | 2928 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | copy fasta | chr4 | 83531108 | 83610875 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0010g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0010g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0011g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0012g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0013g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0014g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0001t0015g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0001c0004t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0002c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0002c0002t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0002c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0002c0002t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0002c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0003c0003t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| a0003c0003t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0206 | EUR | GBR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0267 | EUR | GBR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0293 | EUR | GBR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0149 | EUR | GBR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | FIN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0212 | EUR | FIN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0328 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0290 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0307 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0202 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01256 | hp2 | a0001 | c0001 | t0010 | g0268 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01257 | hp2 | a0002 | c0002 | t0003 | g0167 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01258 | hp2 | a0002 | c0002 | t0003 | g0168 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0246 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0292 | EUR | IBS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0254 | EUR | IBS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG01993 | hp2 | a0003 | c0003 | t0002 | g0284 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0003 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | CDX | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0283 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0208 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0205 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0297 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0330 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02735 | hp1 | a0001 | c0001 | t0011 | g0275 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0004 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0333 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0245 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0247 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0289 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0191 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03579 | hp2 | a0001 | c0004 | t0004 | g0306 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0294 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0302 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0322 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0327 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0319 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | CHB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CHB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0065 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18956 | hp1 | a0001 | c0001 | t0008 | g0173 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18988 | hp1 | a0001 | c0001 | t0013 | g0140 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18991 | hp2 | a0001 | c0001 | t0008 | g0143 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0331 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0179 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ASW | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ASW | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0304 | EUR | TSI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0291 | EUR | TSI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | GIH | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0249 | SAS | GIH | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0310 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | USA | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | USA | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | USA | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0204 | AFR | USA | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0195 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0133 | REF | REF | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0080 | REF | REF | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:83544578
|
A | G | 1 | a0003 | 2 | HG01993.hp2 HG02300.hp1 |
missense_variant | MODERATE | c.184A>G | p.Ile62Val | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/12 | 699/2928 | 184/1305 | 62/434 | chr4 | 83544578 | ||
| chr4:83598675
|
G | A | 1 | a0002 | 5 | HG01192.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
missense_variant | MODERATE | c.1157G>A | p.Arg386Lys | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/12 | 1672/2928 | 1157/1305 | 386/434 | chr4 | 83598675 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:83594850
|
C | G | 1 | a0001c0004 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.744C>G | p.Gly248Gly | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/12 | 1259/2928 | 744/1305 | 248/434 | chr4 | 83594850 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:83536131
|
C | G | 2 | a0001c0001t0014a0001c0001t0015 | 2 | HG02055.hp1 HG02809.hp1 |
5_prime_UTR_variant | MODIFIER | c.-492C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/12 | 492 | chr4 | 83536131 | |||||
| chr4:83536133
|
G | C | 2 | a0001c0001t0007a0001c0001t0009 | 5 | HG02622.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-490G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/12 | chr4 | 83536133 | ||||||
| chr4:83536203
|
C | G | 1 | a0001c0001t0009 | 2 | HG03130.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-420C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/12 | 420 | chr4 | 83536203 | |||||
| chr4:83536412
|
TTAA | T | 1 | a0001c0001t0008 | 3 | NA18948.hp1 NA18956.hp1 NA18991.hp2 |
5_prime_UTR_variant | MODIFIER | c.-210_-208delTAA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/12 | 208 | chr4 | 83536412 | |||||
| chr4:83536416
|
C | G | 1 | a0001c0001t0008 | 3 | NA18948.hp1 NA18956.hp1 NA18991.hp2 |
5_prime_UTR_variant | MODIFIER | c.-207C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/12 | 207 | chr4 | 83536416 | |||||
| chr4:83604820
|
CT | C | 7 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(4): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*60delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 60 | INFO_REALIGN_3_PRIME | chr4 | 83604820 | ||||
| chr4:83604860
|
A | G | 1 | a0001c0001t0010 | 2 | HG01256.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*93A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 93 | chr4 | 83604860 | |||||
| chr4:83605122
|
T | C | 12 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(9): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*355T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 355 | chr4 | 83605122 | |||||
| chr4:83605348
|
C | T | 1 | a0001c0001t0013 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 581 | chr4 | 83605348 | |||||
| chr4:83605383
|
C | T | 2 | a0001c0001t0003a0002c0002t0003 | 75 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*616C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 616 | chr4 | 83605383 | |||||
| chr4:83605420
|
A | G | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(11): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*653A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 653 | chr4 | 83605420 | |||||
| chr4:83605547
|
T | TA | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(3): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*792dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 793 | INFO_REALIGN_3_PRIME | chr4 | 83605547 | ||||
| chr4:83605614
|
C | T | 5 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(2): Show | 103 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*847C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 847 | chr4 | 83605614 | |||||
| chr4:83605707
|
A | C | 1 | a0001c0001t0006 | 4 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*940A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 940 | chr4 | 83605707 | |||||
| chr4:83605844
|
T | G | 1 | a0001c0001t0012 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1077T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 1077 | chr4 | 83605844 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:83536848
|
A | G | 97 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.141+85A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83536848 | ||||||
| chr4:83536875
|
C | G | 97 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.141+112C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83536875 | ||||||
| chr4:83536880
|
G | A | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.141+117G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83536880 | ||||||
| chr4:83536940
|
G | T | 1 | a0001c0001t0001g0237 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.141+177G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83536940 | ||||||
| chr4:83537228
|
C | G | 9 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(6): Show | 9 | HG02258.hp2 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+465C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537228 | ||||||
| chr4:83537348
|
C | G | 31 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0209others(28): Show | 31 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.141+585C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537348 | ||||||
| chr4:83537563
|
TA | T | 9 | a0001c0001t0003g0196a0001c0001t0004g0198a0001c0001t0004g0199others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.141+809delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537563 | |||||
| chr4:83537564
|
A | T | 13 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0222others(10): Show | 13 | HG02027.hp2 HG02145.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+801A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537564 | ||||||
| chr4:83537589
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0005g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.141+827_141+828ins others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537589 | |||||
| chr4:83537591
|
A | ATG | 34 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0153others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.141+862_141+863dup others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | |||||
| chr4:83537591
|
A | ATGTG | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0002g0330others(1): Show | 4 | HG01175.hp2 HG02717.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+860_141+863dup others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | |||||
| chr4:83537591
|
A | ATGTGTG | 5 | a0001c0001t0001g0178a0001c0001t0003g0177a0001c0001t0003g0180others(2): Show | 5 | HG00642.hp1 HG00741.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+858_141+863dup others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | |||||
| chr4:83537591
|
A | ATGTGTGT others(1): Show |
10 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0185others(7): Show | 10 | HG00733.hp2 HG02486.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+856_141+863dup others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | |||||
| chr4:83537591
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0005g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.141+854_141+863dup others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | |||||
| chr4:83537591
|
A | G | 36 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0209others(33): Show | 36 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.141+828A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537591 | ||||||
| chr4:83537591
|
ATG | A | 21 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0003g0016others(18): Show | 21 | HG00438.hp2 HG00597.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.141+862_141+863del others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | |||||
| chr4:83537591
|
ATGTG | A | 5 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(2): Show | 5 | HG02258.hp1 NA18612.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+860_141+863del others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | |||||
| chr4:83537591
|
ATGTGTG | A | 9 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0007g0009others(6): Show | 9 | HG02055.hp1 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+858_141+863del others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | |||||
| chr4:83537593
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.141+830G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537593 | ||||||
| chr4:83537621
|
G | GTA | 6 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(3): Show | 6 | HG02896.hp1 HG02897.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+859_141+860ins others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537621 | |||||
| chr4:83537623
|
G | A | 7 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(4): Show | 7 | HG02896.hp1 HG02897.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+860G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537623 | ||||||
| chr4:83537623
|
G | GTA | 83 | a0001c0001t0001g0255a0001c0001t0001g0298a0001c0001t0001g0301others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.141+861_141+862ins others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537623 | |||||
| chr4:83537625
|
G | A | 115 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.141+862G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537625 | ||||||
| chr4:83537625
|
G | GTA | 3 | a0001c0001t0002g0216a0001c0001t0002g0236a0001c0001t0002g0329 | 3 | HG03041.hp1 NA19006.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+866_141+867dup others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537625 | |||||
| chr4:83537625
|
G | GTATA | 3 | a0001c0001t0002g0238a0001c0001t0003g0327a0001c0001t0003g0328 | 3 | HG01169.hp2 HG04228.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.141+864_141+867dup others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537625 | |||||
| chr4:83537625
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0003g0193a0001c0001t0004g0194 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.141+863_141+864ins others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537625 | |||||
| chr4:83537627
|
A | G | 3 | a0001c0001t0001g0172a0001c0001t0002g0192a0001c0001t0003g0176 | 3 | HG00280.hp1 HG02970.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.141+864A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537627 | ||||||
| chr4:83537706
|
G | C | 1 | a0001c0001t0002g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.141+943G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537706 | ||||||
| chr4:83537733
|
G | T | 1 | a0001c0001t0002g0238 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.141+970G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537733 | ||||||
| chr4:83537746
|
C | T | 2 | a0001c0001t0002g0332a0001c0001t0005g0331 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.141+983C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537746 | ||||||
| chr4:83537784
|
C | T | 5 | a0001c0001t0007g0009a0001c0001t0007g0204a0001c0001t0007g0205others(2): Show | 5 | HG02622.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+1021C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537784 | ||||||
| chr4:83537805
|
T | A | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.141+1042T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537805 | ||||||
| chr4:83537817
|
G | A | 1 | a0001c0001t0012g0245 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.141+1054G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537817 | ||||||
| chr4:83537848
|
T | C | 2 | a0001c0001t0002g0332a0001c0001t0005g0331 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.141+1085T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537848 | ||||||
| chr4:83538095
|
A | T | 1 | a0001c0001t0003g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.141+1332A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538095 | ||||||
| chr4:83538365
|
A | G | 5 | a0001c0001t0003g0014a0001c0001t0005g0005a0001c0001t0005g0006others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+1602A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538365 | ||||||
| chr4:83538479
|
C | T | 1 | a0001c0001t0002g0326 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.141+1716C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538479 | ||||||
| chr4:83538562
|
G | A | 3 | a0001c0001t0005g0206a0001c0001t0014g0004a0001c0001t0015g0003 | 3 | HG00099.hp1 HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.141+1799G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538562 | ||||||
| chr4:83538689
|
A | G | 1 | a0001c0001t0002g0325 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.141+1926A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538689 | ||||||
| chr4:83538713
|
C | A | 2 | a0001c0001t0002g0332a0001c0001t0005g0331 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.141+1950C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538713 | ||||||
| chr4:83538713
|
C | G | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.141+1950C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538713 | ||||||
| chr4:83538797
|
A | C | 97 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.141+2034A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538797 | ||||||
| chr4:83538804
|
T | G | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.141+2041T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538804 | ||||||
| chr4:83538864
|
A | C | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.141+2101A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538864 | ||||||
| chr4:83538942
|
A | T | 9 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(6): Show | 9 | HG02258.hp2 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+2179A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538942 | ||||||
| chr4:83539018
|
T | C | 2 | a0001c0001t0003g0193a0001c0001t0004g0194 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.141+2255T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539018 | ||||||
| chr4:83539041
|
A | G | 97 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.141+2278A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539041 | ||||||
| chr4:83539060
|
G | A | 2 | a0001c0001t0002g0332a0001c0001t0005g0331 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.141+2297G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539060 | ||||||
| chr4:83539268
|
G | A | 2 | a0001c0001t0002g0216a0001c0001t0006g0207 | 2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.141+2505G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539268 | ||||||
| chr4:83539350
|
C | A | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.141+2587C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539350 | ||||||
| chr4:83539381
|
C | T | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.141+2618C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539381 | ||||||
| chr4:83539820
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.141+3057C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539820 | ||||||
| chr4:83539924
|
G | A | 41 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0209others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.141+3161G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539924 | ||||||
| chr4:83539924
|
G | C | 1 | a0001c0001t0003g0182 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.141+3161G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539924 | ||||||
| chr4:83539947
|
T | C | 162 | a0001c0001t0001g0178a0001c0001t0001g0225a0001c0001t0001g0226others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.141+3184T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539947 | ||||||
| chr4:83539962
|
G | A | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.141+3199G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539962 | ||||||
| chr4:83540112
|
A | G | 94 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.141+3349A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540112 | ||||||
| chr4:83540155
|
T | TA | 16 | a0001c0001t0001g0037a0001c0001t0001g0150a0001c0001t0001g0152others(13): Show | 16 | HG00438.hp2 HG00741.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.141+3414dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83540155 | |||||
| chr4:83540155
|
TA | T | 7 | a0001c0001t0001g0146a0001c0001t0002g0324a0001c0001t0002g0330others(4): Show | 7 | HG01891.hp1 HG02717.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+3414delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83540155 | |||||
| chr4:83540155
|
TAA | T | 33 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0209others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.141+3413_141+3414d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83540155 | |||||
| chr4:83540310
|
G | A | 1 | a0001c0001t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.141+3547G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540310 | ||||||
| chr4:83540354
|
C | T | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.141+3591C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540354 | ||||||
| chr4:83540550
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.141+3787C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540550 | ||||||
| chr4:83540560
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.141+3797G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540560 | ||||||
| chr4:83540627
|
C | T | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.141+3864C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540627 | ||||||
| chr4:83540722
|
G | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.142-3814G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540722 | ||||||
| chr4:83540761
|
C | T | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-3775C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540761 | ||||||
| chr4:83540857
|
T | C | 94 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.142-3679T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540857 | ||||||
| chr4:83540974
|
A | G | 136 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.142-3562A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540974 | ||||||
| chr4:83540981
|
T | C | 162 | a0001c0001t0001g0178a0001c0001t0001g0225a0001c0001t0001g0226others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.142-3555T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540981 | ||||||
| chr4:83540989
|
T | C | 94 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.142-3547T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540989 | ||||||
| chr4:83541087
|
C | T | 1 | a0001c0001t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.142-3449C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541087 | ||||||
| chr4:83541175
|
A | G | 94 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.142-3361A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541175 | ||||||
| chr4:83541246
|
T | G | 1 | a0001c0001t0002g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.142-3290T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541246 | ||||||
| chr4:83541376
|
C | A | 1 | a0002c0002t0003g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.142-3160C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541376 | ||||||
| chr4:83541393
|
C | CT | 17 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0145others(14): Show | 17 | HG01175.hp2 HG02055.hp1 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.142-3123dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83541393 | |||||
| chr4:83541393
|
C | CTT | 86 | a0001c0001t0001g0240a0001c0001t0001g0243a0001c0001t0001g0255others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.142-3124_142-3123d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83541393 | |||||
| chr4:83541393
|
C | CTTT | 8 | a0001c0001t0001g0242a0001c0001t0002g0318a0001c0001t0002g0320others(5): Show | 8 | HG00642.hp2 HG02559.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-3125_142-3123d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83541393 | |||||
| chr4:83541393
|
CT | C | 30 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0209others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-3123delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83541393 | |||||
| chr4:83541451
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.142-3085C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541451 | ||||||
| chr4:83541672
|
G | A | 1 | a0001c0001t0002g0330 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.142-2864G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541672 | ||||||
| chr4:83541759
|
C | A | 1 | a0001c0001t0003g0040 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.142-2777C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541759 | ||||||
| chr4:83541792
|
C | T | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-2744C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541792 | ||||||
| chr4:83541874
|
G | A | 2 | a0001c0001t0003g0014a0001c0001t0005g0005 | 2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.142-2662G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541874 | ||||||
| chr4:83542013
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0145 | 3 | NA18949.hp2 NA18977.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.142-2523A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542013 | ||||||
| chr4:83542041
|
T | TG | 6 | a0001c0001t0002g0330a0001c0001t0003g0014a0001c0001t0005g0005others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-2490dupG | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83542041 | |||||
| chr4:83542056
|
C | T | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-2480C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542056 | ||||||
| chr4:83542089
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.142-2447C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542089 | ||||||
| chr4:83542740
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.142-1796A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542740 | ||||||
| chr4:83542814
|
A | G | 31 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0209others(28): Show | 31 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.142-1722A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542814 | ||||||
| chr4:83542851
|
G | A | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-1685G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542851 | ||||||
| chr4:83542871
|
G | C | 1 | a0001c0001t0002g0253 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.142-1665G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542871 | ||||||
| chr4:83542937
|
G | A | 19 | a0001c0001t0001g0178a0001c0001t0002g0183a0001c0001t0002g0184others(16): Show | 19 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.142-1599G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542937 | ||||||
| chr4:83542986
|
G | A | 6 | a0001c0001t0002g0330a0001c0001t0003g0014a0001c0001t0005g0005others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-1550G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542986 | ||||||
| chr4:83542993
|
C | G | 2 | a0001c0001t0002g0332a0001c0001t0005g0331 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.142-1543C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542993 | ||||||
| chr4:83543030
|
T | G | 163 | a0001c0001t0001g0178a0001c0001t0001g0225a0001c0001t0001g0226others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.142-1506T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543030 | ||||||
| chr4:83543038
|
C | T | 1 | a0001c0001t0003g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.142-1498C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543038 | ||||||
| chr4:83543059
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.142-1477G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543059 | ||||||
| chr4:83543283
|
C | T | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-1253C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543283 | ||||||
| chr4:83543319
|
G | A | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-1217G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543319 | ||||||
| chr4:83543322
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142-1214C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543322 | ||||||
| chr4:83543337
|
G | C | 6 | a0001c0001t0002g0330a0001c0001t0003g0014a0001c0001t0005g0005others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-1199G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543337 | ||||||
| chr4:83543471
|
C | T | 2 | a0001c0001t0014g0004a0001c0001t0015g0003 | 2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.142-1065C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543471 | ||||||
| chr4:83543521
|
C | T | 1 | a0001c0001t0002g0330 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.142-1015C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543521 | ||||||
| chr4:83543857
|
T | C | 1 | a0001c0001t0002g0318 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.142-679T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543857 | ||||||
| chr4:83543880
|
A | T | 1 | a0001c0001t0002g0317 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.142-656A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543880 | ||||||
| chr4:83543997
|
A | G | 3 | a0001c0001t0003g0014a0001c0001t0005g0005a0001c0001t0005g0006 | 3 | HG02258.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.142-539A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543997 | ||||||
| chr4:83544083
|
C | T | 95 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-453C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544083 | ||||||
| chr4:83544241
|
C | A | 1 | a0001c0001t0002g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142-295C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544241 | ||||||
| chr4:83544308
|
G | A | 1 | a0001c0001t0005g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142-228G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544308 | ||||||
| chr4:83544316
|
A | G | 5 | a0001c0001t0007g0009a0001c0001t0007g0204a0001c0001t0007g0205others(2): Show | 5 | HG02622.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-220A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544316 | ||||||
| chr4:83544460
|
C | T | 94 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.142-76C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544460 | ||||||
| chr4:83544501
|
G | C | 1 | a0001c0001t0006g0207 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-35G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544501 | ||||||
| chr4:83544702
|
A | C | 94 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.208+100A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83544702 | ||||||
| chr4:83544730
|
C | A | 1 | a0001c0001t0005g0319 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.208+128C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83544730 | ||||||
| chr4:83544863
|
G | A | 3 | a0001c0001t0004g0041a0001c0001t0004g0042a0001c0001t0004g0043 | 3 | HG02145.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.208+261G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83544863 | ||||||
| chr4:83545076
|
A | T | 3 | a0001c0001t0002g0248a0001c0001t0002g0315a0001c0001t0002g0316 | 3 | HG02004.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.208+474A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545076 | ||||||
| chr4:83545178
|
C | T | 4 | a0001c0001t0002g0332a0001c0001t0003g0193a0001c0001t0004g0194others(1): Show | 4 | HG02451.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+576C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545178 | ||||||
| chr4:83545247
|
C | A | 1 | a0001c0001t0003g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.208+645C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545247 | ||||||
| chr4:83545261
|
C | T | 3 | a0001c0001t0003g0014a0001c0001t0005g0005a0001c0001t0005g0006 | 3 | HG02258.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.208+659C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545261 | ||||||
| chr4:83545444
|
T | TA | 114 | a0001c0001t0001g0178a0001c0001t0001g0240a0001c0001t0001g0242others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.208+856dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83545444 | |||||
| chr4:83545569
|
A | C | 2 | a0001c0001t0003g0193a0001c0001t0004g0194 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.208+967A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545569 | ||||||
| chr4:83545589
|
T | G | 2 | a0001c0001t0003g0193a0001c0001t0004g0194 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.208+987T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545589 | ||||||
| chr4:83545603
|
G | A | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.208+1001G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545603 | ||||||
| chr4:83545757
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.208+1155C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545757 | ||||||
| chr4:83545825
|
A | G | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.208+1223A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545825 | ||||||
| chr4:83545917
|
T | G | 2 | a0001c0001t0002g0332a0001c0001t0005g0331 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.208+1315T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545917 | ||||||
| chr4:83546120
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.208+1518G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546120 | ||||||
| chr4:83546147
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.208+1545G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546147 | ||||||
| chr4:83546223
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.208+1621G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546223 | ||||||
| chr4:83546307
|
C | T | 2 | a0001c0001t0003g0193a0001c0001t0004g0194 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.208+1705C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546307 | ||||||
| chr4:83546379
|
G | GT | 104 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.208+1793dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83546379 | |||||
| chr4:83546379
|
GT | G | 6 | a0001c0001t0001g0178a0001c0001t0003g0014a0001c0001t0003g0182others(3): Show | 6 | HG00733.hp2 HG02258.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+1793delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83546379 | |||||
| chr4:83546488
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0045a0001c0001t0001g0150 | 3 | HG00741.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.208+1886T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546488 | ||||||
| chr4:83546584
|
C | T | 3 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215 | 3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.208+1982C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546584 | ||||||
| chr4:83546594
|
G | A | 94 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.208+1992G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546594 | ||||||
| chr4:83546698
|
C | T | 94 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.208+2096C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546698 | ||||||
| chr4:83546710
|
A | G | 94 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.208+2108A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546710 | ||||||
| chr4:83546771
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.208+2169G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546771 | ||||||
| chr4:83546791
|
T | C | 1 | a0001c0001t0005g0195 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208+2189T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546791 | ||||||
| chr4:83547003
|
C | T | 29 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0209others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.208+2401C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547003 | ||||||
| chr4:83547064
|
C | T | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.208+2462C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547064 | ||||||
| chr4:83547246
|
C | CT | 26 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(23): Show | 26 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.208+2668dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83547246 | |||||
| chr4:83547246
|
CT | C | 35 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0069others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.208+2668delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83547246 | |||||
| chr4:83547246
|
CTT | C | 79 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(76): Show | 79 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.208+2667_208+2668d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83547246 | |||||
| chr4:83547283
|
T | C | 92 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.208+2681T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547283 | ||||||
| chr4:83547286
|
T | G | 8 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0156others(5): Show | 8 | NA18939.hp1 NA18960.hp2 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+2684T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547286 | ||||||
| chr4:83547292
|
A | G | 3 | a0001c0001t0005g0197a0001c0001t0007g0204a0001c0001t0007g0205 | 3 | HG02622.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.208+2690A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547292 | ||||||
| chr4:83547341
|
C | T | 4 | a0001c0001t0004g0307a0001c0001t0005g0241a0001c0001t0005g0247others(1): Show | 4 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+2739C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547341 | ||||||
| chr4:83547346
|
A | G | 4 | a0001c0001t0004g0307a0001c0001t0005g0241a0001c0001t0005g0247others(1): Show | 4 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+2744A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547346 | ||||||
| chr4:83547348
|
A | G | 6 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0004g0307others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+2746A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547348 | ||||||
| chr4:83547397
|
T | C | 8 | a0001c0001t0003g0196a0001c0001t0004g0198a0001c0001t0004g0199others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+2795T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547397 | ||||||
| chr4:83547402
|
G | A | 3 | a0001c0001t0003g0177a0001c0001t0003g0180a0001c0001t0003g0181 | 3 | HG00642.hp1 HG00741.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.208+2800G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547402 | ||||||
| chr4:83547410
|
G | A | 1 | a0001c0001t0014g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.208+2808G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547410 | ||||||
| chr4:83547414
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.208+2812A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547414 | ||||||
| chr4:83547453
|
C | A | 1 | a0001c0001t0001g0255 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.208+2851C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547453 | ||||||
| chr4:83547463
|
A | C | 1 | a0001c0001t0001g0128 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.208+2861A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547463 | ||||||
| chr4:83547463
|
A | G | 1 | a0001c0001t0002g0329 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.208+2861A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547463 | ||||||
| chr4:83547464
|
G | A | 14 | a0001c0001t0002g0015a0001c0001t0003g0017a0001c0001t0003g0018others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.208+2862G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547464 | ||||||
| chr4:83547479
|
C | T | 143 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.208+2877C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547479 | ||||||
| chr4:83547487
|
T | C | 7 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(4): Show | 7 | HG00099.hp1 HG02717.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+2885T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547487 | ||||||
| chr4:83547494
|
T | C | 2 | a0001c0001t0002g0330a0001c0001t0005g0206 | 2 | HG00099.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.208+2892T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547494 | ||||||
| chr4:83547499
|
A | G | 237 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.208+2897A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547499 | ||||||
| chr4:83547503
|
C | T | 210 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.208+2901C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547503 | ||||||
| chr4:83547504
|
G | A | 210 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.208+2902G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547504 | ||||||
| chr4:83547532
|
G | A | 176 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.208+2930G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547532 | ||||||
| chr4:83547538
|
T | C | 8 | a0001c0001t0003g0196a0001c0001t0004g0198a0001c0001t0004g0199others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+2936T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547538 | ||||||
| chr4:83547547
|
T | C | 2 | a0001c0001t0002g0248a0001c0001t0002g0264 | 2 | HG00408.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.208+2945T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547547 | ||||||
| chr4:83547806
|
C | A | 2 | a0001c0001t0002g0265a0001c0001t0002g0266 | 2 | NA18951.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.208+3204C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547806 | ||||||
| chr4:83547806
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.208+3204C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547806 | ||||||
| chr4:83547807
|
G | A | 5 | a0001c0001t0004g0307a0001c0001t0005g0195a0001c0001t0005g0241others(2): Show | 5 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+3205G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547807 | ||||||
| chr4:83547853
|
CT | C | 77 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.208+3268delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83547853 | |||||
| chr4:83547853
|
CTT | C | 118 | a0001c0001t0001g0048a0001c0001t0001g0225a0001c0001t0001g0226others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.208+3267_208+3268d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83547853 | |||||
| chr4:83548053
|
C | G | 1 | a0001c0001t0005g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.208+3451C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548053 | ||||||
| chr4:83548285
|
T | C | 5 | a0001c0001t0003g0014a0001c0001t0003g0193a0001c0001t0004g0310others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+3683T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548285 | ||||||
| chr4:83548699
|
C | T | 74 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(71): Show | 74 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.208+4097C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548699 | ||||||
| chr4:83548917
|
C | G | 74 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(71): Show | 74 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.208+4315C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548917 | ||||||
| chr4:83548983
|
T | A | 1 | a0001c0001t0003g0034 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.208+4381T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548983 | ||||||
| chr4:83548990
|
AC | A | 21 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.208+4389delC | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548990 | ||||||
| chr4:83549031
|
A | C | 1 | a0001c0001t0005g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.208+4429A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549031 | ||||||
| chr4:83549038
|
GTGACAGA others(13): Show |
G | 1 | a0001c0001t0005g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.208+4438_208+4457d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549038 | |||||
| chr4:83549160
|
C | A | 1 | a0001c0001t0002g0258 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.208+4558C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549160 | ||||||
| chr4:83549166
|
G | GAAA | 112 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.208+4576_208+4578d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549166 | |||||
| chr4:83549166
|
GA | G | 14 | a0001c0001t0002g0112a0001c0001t0002g0183a0001c0001t0002g0189others(11): Show | 14 | HG00099.hp1 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+4578delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549166 | |||||
| chr4:83549229
|
T | A | 1 | a0001c0001t0013g0140 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.208+4627T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549229 | ||||||
| chr4:83549444
|
C | CGT | 70 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0059others(67): Show | 70 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.208+4865_208+4866d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549444 | |||||
| chr4:83549444
|
C | CGTGT | 23 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.208+4863_208+4866d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549444 | |||||
| chr4:83549444
|
CGT | C | 4 | a0001c0001t0002g0211a0001c0001t0005g0206a0001c0001t0005g0219others(1): Show | 4 | HG00099.hp1 HG03710.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+4865_208+4866d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549444 | |||||
| chr4:83549444
|
CGTGT | C | 3 | a0001c0001t0004g0194a0001c0001t0009g0007a0001c0001t0009g0008 | 3 | HG02451.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.208+4863_208+4866d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549444 | |||||
| chr4:83549465
|
GTGTA | G | 15 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0184others(12): Show | 15 | HG00140.hp1 HG01109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.208+4869_208+4872d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549465 | |||||
| chr4:83549467
|
GTA | G | 79 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(76): Show | 79 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.208+4867_208+4868d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549467 | |||||
| chr4:83549469
|
A | G | 21 | a0001c0001t0002g0223a0001c0001t0002g0227a0001c0001t0002g0229others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.208+4867A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549469 | ||||||
| chr4:83549471
|
GTATA | G | 4 | a0001c0001t0002g0223a0001c0001t0002g0227a0001c0001t0002g0312others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+4877_208+4880d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549471 | |||||
| chr4:83549473
|
A | G | 111 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.208+4871A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549473 | ||||||
| chr4:83549475
|
A | G | 11 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(8): Show | 11 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+4873A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549475 | ||||||
| chr4:83549477
|
A | G | 11 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(8): Show | 11 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+4875A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549477 | ||||||
| chr4:83549479
|
A | G | 11 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(8): Show | 11 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+4877A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549479 | ||||||
| chr4:83549620
|
C | G | 1 | a0001c0001t0004g0203 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.208+5018C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549620 | ||||||
| chr4:83549622
|
T | C | 1 | a0001c0001t0004g0203 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.208+5020T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549622 | ||||||
| chr4:83549623
|
C | T | 1 | a0001c0001t0004g0203 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.208+5021C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549623 | ||||||
| chr4:83549680
|
T | C | 190 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.208+5078T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549680 | ||||||
| chr4:83549711
|
T | TTTA | 7 | a0001c0001t0003g0026a0001c0001t0003g0050a0001c0001t0003g0051others(4): Show | 7 | HG02257.hp1 HG02602.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+5124_208+5126d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | |||||
| chr4:83549711
|
T | TTTATTA | 92 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(89): Show | 92 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.208+5121_208+5126d others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | |||||
| chr4:83549711
|
T | TTTATTAT others(2): Show |
6 | a0001c0001t0002g0248a0001c0001t0002g0259a0001c0001t0002g0267others(3): Show | 6 | HG00099.hp2 HG01256.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+5118_208+5126d others(11): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | |||||
| chr4:83549711
|
T | TTTATTAT others(5): Show |
1 | a0001c0001t0002g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.208+5115_208+5126d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | |||||
| chr4:83549711
|
T | TTTATTAT others(8): Show |
3 | a0001c0001t0005g0179a0001c0001t0012g0245a0001c0004t0004g0306 | 3 | HG03041.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208+5112_208+5126d others(17): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | |||||
| chr4:83549711
|
T | TTTATTAT others(11): Show |
6 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0234others(3): Show | 6 | HG02055.hp1 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+5126_208+5127i others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | |||||
| chr4:83549711
|
T | TTTATTAT others(14): Show |
4 | a0001c0001t0002g0231a0001c0001t0002g0235a0001c0001t0002g0236others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+5126_208+5127i others(23): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | |||||
| chr4:83549711
|
T | TTTATTAT others(20): Show |
2 | a0001c0001t0002g0229a0001c0001t0002g0230 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.208+5126_208+5127i others(29): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | |||||
| chr4:83549729
|
G | A | 188 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.208+5127G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549729 | ||||||
| chr4:83549822
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0145 | 3 | NA18949.hp2 NA18977.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.208+5220A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549822 | ||||||
| chr4:83550100
|
AGTGATTC others(19): Show |
A | 1 | a0001c0001t0004g0203 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.208+5502_208+5527d others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83550100 | |||||
| chr4:83551109
|
C | T | 2 | a0001c0001t0003g0071a0001c0001t0003g0144 | 2 | HG01081.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.208+6507C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551109 | ||||||
| chr4:83551118
|
A | G | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.208+6516A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551118 | ||||||
| chr4:83551315
|
A | G | 1 | a0001c0001t0015g0003 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.208+6713A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551315 | ||||||
| chr4:83551487
|
ATT | A | 105 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.208+6892_208+6893d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551487 | |||||
| chr4:83551490
|
T | A | 105 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.208+6888T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551490 | ||||||
| chr4:83551603
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.208+7001C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551603 | ||||||
| chr4:83551662
|
C | T | 74 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(71): Show | 74 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.208+7060C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551662 | ||||||
| chr4:83551665
|
C | A | 115 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.208+7063C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551665 | ||||||
| chr4:83551706
|
C | T | 1 | a0001c0001t0004g0215 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.208+7104C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551706 | ||||||
| chr4:83551793
|
G | GA | 12 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0122others(9): Show | 12 | HG01175.hp1 HG02615.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+7212dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551793 | |||||
| chr4:83551793
|
GA | G | 14 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0125others(11): Show | 14 | HG01496.hp2 HG02015.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+7212delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551793 | |||||
| chr4:83551813
|
A | AAAAATCT others(8): Show |
3 | a0001c0001t0001g0225a0001c0001t0005g0179a0001c0001t0005g0224 | 3 | HG02572.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208+7212_208+7213i others(17): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAAAATCT others(16): Show |
4 | a0001c0001t0002g0227a0001c0001t0002g0311a0001c0001t0002g0334others(1): Show | 4 | HG02027.hp2 HG02145.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(25): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAAATCTA others(3): Show |
2 | a0001c0001t0002g0251a0001c0001t0002g0276 | 2 | HG03490.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.208+7212_208+7213i others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAAATCTA others(7): Show |
18 | a0001c0001t0001g0226a0001c0001t0001g0240a0001c0001t0001g0242others(15): Show | 18 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAAATCTA others(11): Show |
25 | a0001c0001t0001g0298a0001c0001t0001g0301a0001c0001t0002g0185others(22): Show | 25 | HG01070.hp2 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAAATCTA others(15): Show |
27 | a0001c0001t0001g0308a0001c0001t0002g0025a0001c0001t0002g0184others(24): Show | 27 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAAATCTA others(19): Show |
1 | a0001c0001t0002g0324 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.208+7212_208+7213i others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAATCT | 6 | a0001c0001t0001g0160a0001c0001t0003g0014a0001c0001t0003g0193others(3): Show | 6 | HG02258.hp1 HG03209.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAATCTAT others(2): Show |
15 | a0001c0001t0002g0015a0001c0001t0002g0250a0001c0001t0002g0260others(12): Show | 15 | HG00438.hp2 HG01993.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(11): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAATCTAT others(6): Show |
10 | a0001c0001t0002g0244a0001c0001t0002g0252a0001c0001t0002g0257others(7): Show | 10 | HG00408.hp1 NA18944.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAATCTAT others(10): Show |
2 | a0001c0001t0002g0259a0001c0001t0002g0277 | 2 | HG02040.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.208+7212_208+7213i others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AAATCTAT others(14): Show |
1 | a0001c0001t0003g0328 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.208+7212_208+7213i others(23): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AATCT | 21 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(18): Show | 21 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.208+7244_208+7247d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AATCTATC others(1): Show |
16 | a0001c0001t0002g0039a0001c0001t0002g0183a0001c0001t0002g0189others(13): Show | 16 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.208+7240_208+7247d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AATCTATC others(5): Show |
3 | a0001c0001t0002g0211a0001c0001t0002g0286a0001c0001t0009g0008 | 3 | HG03130.hp1 HG03710.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.208+7236_208+7247d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
A | AATCTATC others(9): Show |
2 | a0001c0001t0005g0219a0001c0001t0009g0007 | 2 | NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.208+7232_208+7247d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551813
|
AATCTATC others(5): Show |
A | 3 | a0001c0001t0005g0036a0001c0001t0014g0004a0001c0001t0015g0003 | 3 | HG02055.hp1 HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.208+7236_208+7247d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | |||||
| chr4:83551814
|
ATCTATCT others(4): Show |
A | 10 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(7): Show | 10 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+7213_208+7223d others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551814 | ||||||
| chr4:83551959
|
G | A | 1 | a0001c0001t0002g0330 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.208+7357G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551959 | ||||||
| chr4:83551999
|
G | C | 1 | a0001c0001t0005g0224 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.208+7397G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551999 | ||||||
| chr4:83552078
|
C | G | 2 | a0001c0001t0003g0013a0001c0001t0003g0053 | 2 | NA18977.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.208+7476C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552078 | ||||||
| chr4:83552208
|
C | T | 3 | a0001c0001t0002g0311a0001c0001t0002g0314a0001c0001t0002g0323 | 3 | NA18947.hp2 NA18975.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.208+7606C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552208 | ||||||
| chr4:83552238
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0125 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.208+7636G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552238 | ||||||
| chr4:83552286
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.208+7684C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552286 | ||||||
| chr4:83552423
|
G | A | 5 | a0001c0001t0002g0211a0001c0001t0005g0206a0001c0001t0005g0219others(2): Show | 5 | HG00099.hp1 HG03130.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+7821G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552423 | ||||||
| chr4:83552760
|
C | A | 1 | a0001c0001t0002g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.208+8158C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552760 | ||||||
| chr4:83552950
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.208+8348C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552950 | ||||||
| chr4:83553088
|
A | G | 2 | a0001c0001t0014g0004a0001c0001t0015g0003 | 2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.208+8486A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553088 | ||||||
| chr4:83553095
|
T | C | 17 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+8493T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553095 | ||||||
| chr4:83553223
|
T | C | 10 | a0001c0001t0004g0307a0001c0001t0005g0179a0001c0001t0005g0195others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+8621T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553223 | ||||||
| chr4:83553226
|
T | C | 17 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+8624T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553226 | ||||||
| chr4:83553421
|
A | G | 5 | a0001c0001t0003g0014a0001c0001t0003g0193a0001c0001t0004g0310others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+8819A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553421 | ||||||
| chr4:83553442
|
T | C | 6 | a0001c0001t0002g0155a0001c0001t0002g0260a0001c0001t0002g0261others(3): Show | 6 | NA18943.hp2 NA18948.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+8840T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553442 | ||||||
| chr4:83553481
|
G | A | 10 | a0001c0001t0004g0307a0001c0001t0005g0179a0001c0001t0005g0195others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+8879G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553481 | ||||||
| chr4:83553593
|
A | G | 10 | a0001c0001t0004g0307a0001c0001t0005g0179a0001c0001t0005g0195others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+8991A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553593 | ||||||
| chr4:83553616
|
AG | A | 7 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+9016delG | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83553616 | |||||
| chr4:83553641
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208+9039G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553641 | ||||||
| chr4:83553814
|
G | A | 32 | a0001c0001t0001g0153a0001c0001t0003g0010a0001c0001t0003g0011others(29): Show | 32 | HG00597.hp1 HG00609.hp1 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.208+9212G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553814 | ||||||
| chr4:83553843
|
C | G | 7 | a0001c0001t0001g0067a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG01168.hp1 HG01169.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+9241C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553843 | ||||||
| chr4:83553972
|
A | T | 2 | a0001c0001t0003g0294a0001c0001t0003g0302 | 2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.208+9370A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553972 | ||||||
| chr4:83554504
|
A | C | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG01081.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+9902A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83554504 | ||||||
| chr4:83554741
|
T | C | 1 | a0001c0001t0006g0207 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.208+10139T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83554741 | ||||||
| chr4:83554801
|
C | CT | 53 | a0001c0001t0001g0109a0001c0001t0001g0136a0001c0001t0001g0147others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.208+10219dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83554801 | |||||
| chr4:83554801
|
CTTT | C | 76 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(73): Show | 76 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.208+10217_208+1021 others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83554801 | |||||
| chr4:83554964
|
C | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0078others(3): Show | 6 | HG02698.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+10362C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83554964 | ||||||
| chr4:83555004
|
A | C | 6 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(3): Show | 6 | HG00438.hp1 HG00609.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+10402A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555004 | ||||||
| chr4:83555043
|
A | T | 8 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(5): Show | 8 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+10441A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555043 | ||||||
| chr4:83555150
|
T | C | 2 | a0001c0001t0003g0014a0001c0001t0005g0005 | 2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.208+10548T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555150 | ||||||
| chr4:83555208
|
A | G | 18 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(15): Show | 18 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+10606A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555208 | ||||||
| chr4:83555394
|
TTTAATCA others(10): Show |
T | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+10793_208+1080 others(21): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555394 | ||||||
| chr4:83555470
|
A | G | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+10868A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555470 | ||||||
| chr4:83555562
|
G | A | 1 | a0001c0001t0002g0317 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.208+10960G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555562 | ||||||
| chr4:83555625
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.208+11023G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555625 | ||||||
| chr4:83555707
|
C | T | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+11105C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555707 | ||||||
| chr4:83555790
|
G | A | 6 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+11188G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555790 | ||||||
| chr4:83555809
|
T | C | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+11207T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555809 | ||||||
| chr4:83555824
|
A | G | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+11222A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555824 | ||||||
| chr4:83555840
|
A | G | 2 | a0001c0001t0003g0062a0001c0001t0003g0063 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.208+11238A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555840 | ||||||
| chr4:83556095
|
A | G | 2 | a0001c0001t0010g0246a0001c0001t0010g0268 | 2 | HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.208+11493A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556095 | ||||||
| chr4:83556122
|
A | G | 1 | a0001c0001t0003g0022 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.208+11520A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556122 | ||||||
| chr4:83556245
|
T | C | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.208+11643T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556245 | ||||||
| chr4:83556390
|
T | C | 1 | a0001c0001t0003g0052 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.208+11788T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556390 | ||||||
| chr4:83556562
|
A | ATT | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+11968_208+1196 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83556562 | |||||
| chr4:83556782
|
CA | C | 6 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0002g0324others(3): Show | 6 | HG02258.hp1 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+12194delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83556782 | |||||
| chr4:83556937
|
C | T | 1 | a0001c0001t0003g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.208+12335C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556937 | ||||||
| chr4:83556989
|
C | G | 104 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(101): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.208+12387C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556989 | ||||||
| chr4:83557036
|
C | T | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12434C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557036 | ||||||
| chr4:83557103
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.208+12501C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557103 | ||||||
| chr4:83557119
|
T | G | 5 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+12517T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557119 | ||||||
| chr4:83557272
|
C | A | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12670C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557272 | ||||||
| chr4:83557332
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0124 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.208+12730A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557332 | ||||||
| chr4:83557359
|
T | C | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12757T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557359 | ||||||
| chr4:83557463
|
G | C | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12861G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557463 | ||||||
| chr4:83557511
|
A | G | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12909A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557511 | ||||||
| chr4:83557518
|
TA | T | 87 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(84): Show | 87 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.208+12925delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83557518 | |||||
| chr4:83557527
|
A | T | 67 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(64): Show | 67 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.208+12925A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557527 | ||||||
| chr4:83557583
|
A | G | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12981A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557583 | ||||||
| chr4:83557726
|
A | G | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208+13124A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557726 | ||||||
| chr4:83557834
|
T | C | 1 | a0001c0001t0006g0207 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.208+13232T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557834 | ||||||
| chr4:83557890
|
T | C | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208+13288T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557890 | ||||||
| chr4:83557907
|
C | T | 6 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+13305C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557907 | ||||||
| chr4:83557909
|
G | T | 1 | a0001c0001t0001g0061 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.208+13307G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557909 | ||||||
| chr4:83557967
|
C | G | 18 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(15): Show | 18 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+13365C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557967 | ||||||
| chr4:83558071
|
G | A | 5 | a0001c0001t0002g0155a0001c0001t0002g0260a0001c0001t0002g0261others(2): Show | 5 | NA18943.hp2 NA18948.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+13469G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558071 | ||||||
| chr4:83558213
|
T | A | 1 | a0001c0001t0003g0046 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.208+13611T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558213 | ||||||
| chr4:83558213
|
T | C | 104 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(101): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.208+13611T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558213 | ||||||
| chr4:83558249
|
TG | T | 4 | a0001c0001t0003g0014a0001c0001t0003g0193a0001c0001t0005g0005others(1): Show | 4 | HG02258.hp1 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+13648delG | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558249 | ||||||
| chr4:83558256
|
A | G | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+13654A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558256 | ||||||
| chr4:83558319
|
T | G | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+13717T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558319 | ||||||
| chr4:83558435
|
A | T | 12 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215others(9): Show | 12 | HG01243.hp1 HG02630.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.208+13833A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558435 | ||||||
| chr4:83558540
|
G | A | 83 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(80): Show | 83 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.208+13938G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558540 | ||||||
| chr4:83558765
|
G | A | 102 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.208+14163G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558765 | ||||||
| chr4:83558874
|
C | T | 2 | a0001c0001t0003g0062a0001c0001t0003g0063 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.208+14272C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558874 | ||||||
| chr4:83559046
|
A | G | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208+14444A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559046 | ||||||
| chr4:83559099
|
A | C | 101 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.208+14497A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559099 | ||||||
| chr4:83559120
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.208+14518G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559120 | ||||||
| chr4:83559304
|
A | G | 329 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0045others(326): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.208+14702A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559304 | ||||||
| chr4:83559322
|
G | T | 2 | a0001c0001t0003g0149a0001c0001t0003g0176 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.208+14720G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559322 | ||||||
| chr4:83559347
|
A | G | 29 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(26): Show | 29 | HG00099.hp1 HG01243.hp1 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.208+14745A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559347 | ||||||
| chr4:83559426
|
C | T | 3 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0207 | 3 | HG01891.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.208+14824C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559426 | ||||||
| chr4:83559468
|
C | T | 1 | a0001c0001t0002g0267 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.208+14866C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559468 | ||||||
| chr4:83559489
|
A | G | 1 | a0001c0001t0006g0207 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.208+14887A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559489 | ||||||
| chr4:83559575
|
C | T | 29 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(26): Show | 29 | HG00099.hp1 HG01243.hp1 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.208+14973C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559575 | ||||||
| chr4:83559579
|
C | G | 29 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(26): Show | 29 | HG00099.hp1 HG01243.hp1 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.208+14977C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559579 | ||||||
| chr4:83559678
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.208+15076G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559678 | ||||||
| chr4:83559757
|
C | T | 1 | a0001c0001t0004g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.208+15155C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559757 | ||||||
| chr4:83559831
|
C | T | 71 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.208+15229C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559831 | ||||||
| chr4:83560100
|
C | T | 1 | a0001c0001t0004g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.208+15498C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560100 | ||||||
| chr4:83560116
|
C | T | 11 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 11 | HG00099.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.208+15514C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560116 | ||||||
| chr4:83560294
|
G | A | 1 | a0001c0001t0006g0207 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.208+15692G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560294 | ||||||
| chr4:83560418
|
AT | A | 22 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(19): Show | 22 | HG00099.hp1 HG01243.hp1 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.208+15826delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83560418 | |||||
| chr4:83560549
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.208+15947G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560549 | ||||||
| chr4:83560704
|
G | C | 18 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+16102G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560704 | ||||||
| chr4:83560934
|
C | T | 18 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+16332C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560934 | ||||||
| chr4:83560965
|
G | A | 18 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+16363G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560965 | ||||||
| chr4:83561034
|
C | T | 3 | a0001c0001t0002g0267a0001c0001t0010g0246a0001c0001t0010g0268 | 3 | HG00099.hp2 HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.208+16432C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561034 | ||||||
| chr4:83561052
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.208+16450G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561052 | ||||||
| chr4:83561177
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.208+16575C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561177 | ||||||
| chr4:83561234
|
G | C | 225 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.208+16632G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561234 | ||||||
| chr4:83561301
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.208+16699A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561301 | ||||||
| chr4:83561482
|
C | T | 18 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+16880C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561482 | ||||||
| chr4:83561514
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0110 | 2 | NA18959.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.208+16912G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561514 | ||||||
| chr4:83561587
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.208+16985A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561587 | ||||||
| chr4:83561664
|
A | C | 18 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+17062A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561664 | ||||||
| chr4:83561680
|
A | G | 1 | a0001c0001t0005g0197 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.208+17078A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561680 | ||||||
| chr4:83561819
|
A | AAG | 23 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(20): Show | 23 | HG00099.hp1 HG01243.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.208+17227_208+1722 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83561819 | |||||
| chr4:83561929
|
C | T | 1 | a0001c0001t0003g0322 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.208+17327C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561929 | ||||||
| chr4:83562027
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0136 | 2 | HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.208+17425A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562027 | ||||||
| chr4:83562081
|
G | A | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+17479G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562081 | ||||||
| chr4:83562108
|
C | G | 8 | a0001c0001t0005g0197a0001c0001t0006g0001a0001c0001t0006g0002others(5): Show | 8 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+17506C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562108 | ||||||
| chr4:83562172
|
T | TTATATAT others(57): Show |
2 | a0002c0002t0003g0167a0002c0002t0003g0168 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.208+17623_208+1762 others(68): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562172 | |||||
| chr4:83562179
|
T | TTA | 3 | a0001c0001t0001g0102a0001c0001t0001g0136a0001c0001t0001g0169 | 3 | HG02523.hp2 NA18939.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.208+17596_208+1759 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562179 | |||||
| chr4:83562179
|
T | TTATATAT others(27): Show |
1 | a0001c0001t0001g0101 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.208+17590_208+1762 others(38): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562179 | |||||
| chr4:83562179
|
TTA | T | 92 | a0001c0001t0001g0082a0001c0001t0001g0240a0001c0001t0001g0242others(89): Show | 92 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.208+17596_208+1759 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562179 | |||||
| chr4:83562181
|
A | ATATATAT others(23): Show |
5 | a0001c0001t0001g0069a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG01081.hp1 HG01884.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+17594_208+1762 others(34): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562181 | |||||
| chr4:83562183
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0005g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.208+17593_208+1759 others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562183 | |||||
| chr4:83562183
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0124 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.208+17596_208+1762 others(32): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562183 | |||||
| chr4:83562183
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0001g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208+17623_208+1762 others(60): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562183 | |||||
| chr4:83562183
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0001g0126 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208+17623_208+1762 others(62): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562183 | |||||
| chr4:83562183
|
A | ATATATAT others(53): Show |
1 | a0001c0001t0001g0070 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.208+17623_208+1762 others(64): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562183 | |||||
| chr4:83562188
|
T | TATATATA others(39): Show |
1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.208+17595_208+1759 others(50): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562188 | |||||
| chr4:83562188
|
T | TATATATA others(30): Show |
1 | a0001c0001t0008g0065 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.208+17610_208+1764 others(41): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562188 | |||||
| chr4:83562190
|
TATATATA others(24): Show |
T | 2 | a0001c0001t0001g0048a0001c0001t0003g0181 | 2 | HG00642.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.208+17589_208+1761 others(35): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562190 | ||||||
| chr4:83562190
|
TATATATA others(29): Show |
T | 66 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.208+17589_208+1762 others(40): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562190 | ||||||
| chr4:83562190
|
TATATATA others(33): Show |
T | 2 | a0001c0001t0003g0052a0001c0001t0003g0327 | 2 | HG04228.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.208+17589_208+1762 others(44): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562190 | ||||||
| chr4:83562192
|
TATATATA others(26): Show |
T | 2 | a0001c0001t0005g0179a0001c0001t0012g0245 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208+17598_208+1763 others(37): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562192 | |||||
| chr4:83562193
|
ATATATAA others(38): Show |
A | 7 | a0001c0001t0005g0197a0001c0001t0006g0001a0001c0001t0006g0002others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+17592_208+1763 others(49): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562193 | ||||||
| chr4:83562194
|
T | TA | 17 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0184others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+17593dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562194 | |||||
| chr4:83562195
|
ATATAATA others(36): Show |
A | 1 | a0001c0001t0005g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.208+17594_208+1763 others(47): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562195 | ||||||
| chr4:83562195
|
ATATAATA others(38): Show |
A | 1 | a0001c0001t0006g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.208+17594_208+1763 others(49): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562195 | ||||||
| chr4:83562196
|
TATA | T | 3 | a0001c0001t0002g0183a0001c0001t0002g0190a0001c0001t0002g0192 | 3 | HG02486.hp2 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.208+17598_208+1760 others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562196 | |||||
| chr4:83562196
|
TATAATAT others(22): Show |
T | 3 | a0001c0001t0004g0187a0001c0001t0004g0307a0001c0001t0005g0247 | 3 | HG01243.hp1 HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.208+17598_208+1762 others(33): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562196 | |||||
| chr4:83562198
|
T | A | 9 | a0001c0001t0001g0111a0001c0001t0003g0196a0001c0001t0004g0198others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+17596T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562198 | ||||||
| chr4:83562198
|
TAATATAT others(20): Show |
T | 6 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+17598_208+1762 others(31): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562198 | |||||
| chr4:83562199
|
A | AT | 17 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0184others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+17597_208+1759 others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562199 | ||||||
| chr4:83562199
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208+17597_208+1759 others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562199 | ||||||
| chr4:83562199
|
A | T | 8 | a0001c0001t0003g0196a0001c0001t0004g0198a0001c0001t0004g0199others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+17597A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562199 | ||||||
| chr4:83562199
|
AATATATA others(5): Show |
A | 1 | a0001c0001t0002g0189 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208+17598_208+1760 others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562199 | ||||||
| chr4:83562199
|
AATATATA others(18): Show |
A | 3 | a0001c0001t0005g0195a0001c0001t0005g0319a0001c0001t0005g0333 | 3 | HG02896.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.208+17599_208+1762 others(29): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562199 | |||||
| chr4:83562199
|
AATATATA others(29): Show |
A | 1 | a0001c0001t0003g0057 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.208+17599_208+1763 others(40): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562199 | |||||
| chr4:83562200
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.208+17598A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562200 | ||||||
| chr4:83562204
|
A | AT | 17 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0184others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+17603dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562204 | |||||
| chr4:83562204
|
A | ATATAT | 8 | a0001c0001t0003g0196a0001c0001t0004g0198a0001c0001t0004g0199others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+17603_208+1760 others(9): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562204 | |||||
| chr4:83562210
|
AT | A | 4 | a0001c0001t0002g0183a0001c0001t0002g0190a0001c0001t0002g0192others(1): Show | 4 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+17610delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562210 | |||||
| chr4:83562211
|
T | TA | 22 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0184others(19): Show | 22 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.208+17609_208+1761 others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562211 | ||||||
| chr4:83562211
|
T | TTA | 6 | a0001c0001t0001g0037a0001c0001t0001g0045a0001c0001t0001g0077others(3): Show | 6 | HG00639.hp2 HG00741.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+17622_208+1762 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562211 | |||||
| chr4:83562211
|
T | TTATATAT others(27): Show |
1 | a0001c0001t0001g0165 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208+17623_208+1762 others(38): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562211 | |||||
| chr4:83562211
|
TTATATAT others(19): Show |
T | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.208+17622_208+1764 others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562211 | |||||
| chr4:83562214
|
T | TA | 19 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0184others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.208+17613dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | |||||
| chr4:83562214
|
T | TATATA | 8 | a0001c0001t0003g0196a0001c0001t0004g0198a0001c0001t0004g0199others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+17613_208+1761 others(9): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | |||||
| chr4:83562214
|
T | TATATATA others(2): Show |
88 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.208+17613_208+1762 others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | |||||
| chr4:83562214
|
T | TATATATA others(24): Show |
1 | a0001c0001t0002g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.208+17621_208+1762 others(35): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | |||||
| chr4:83562214
|
T | TATATATA others(24): Show |
3 | a0001c0001t0003g0014a0001c0001t0005g0005a0001c0001t0005g0006 | 3 | HG02258.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.208+17621_208+1762 others(35): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | |||||
| chr4:83562214
|
T | TATATATA others(22): Show |
1 | a0001c0001t0003g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.208+17621_208+1762 others(33): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | |||||
| chr4:83562214
|
T | TATATATA others(28): Show |
1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+17634_208+1763 others(39): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | |||||
| chr4:83562224
|
TA | T | 7 | a0001c0001t0001g0048a0001c0001t0002g0183a0001c0001t0002g0189others(4): Show | 7 | HG00642.hp1 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+17624delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562224 | |||||
| chr4:83562225
|
A | T | 3 | a0001c0001t0005g0195a0001c0001t0005g0319a0001c0001t0005g0333 | 3 | HG02896.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.208+17623A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562225 | ||||||
| chr4:83562228
|
AT | A | 4 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+17627delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562228 | ||||||
| chr4:83562232
|
A | G | 4 | a0001c0001t0003g0014a0001c0001t0003g0193a0001c0001t0005g0005others(1): Show | 4 | HG02258.hp1 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+17630A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562232 | ||||||
| chr4:83562235
|
T | A | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208+17633T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562235 | ||||||
| chr4:83562235
|
TA | T | 4 | a0001c0001t0001g0048a0001c0001t0003g0052a0001c0001t0003g0181others(1): Show | 4 | HG00642.hp1 HG04228.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+17635delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562235 | |||||
| chr4:83562236
|
A | AT | 66 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.208+17634_208+1763 others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562236 | ||||||
| chr4:83562236
|
A | T | 2 | a0001c0001t0001g0075a0001c0001t0003g0057 | 2 | HG02738.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.208+17634A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562236 | ||||||
| chr4:83562237
|
A | T | 3 | a0001c0001t0005g0219a0001c0001t0009g0007a0001c0001t0009g0008 | 3 | HG03130.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.208+17635A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562237 | ||||||
| chr4:83562238
|
T | A | 21 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(18): Show | 21 | HG01243.hp1 HG02486.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.208+17636T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562238 | ||||||
| chr4:83562248
|
T | A | 2 | a0001c0001t0003g0144a0001c0001t0003g0177 | 2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.208+17646T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562248 | ||||||
| chr4:83562775
|
C | G | 1 | a0001c0001t0002g0323 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.208+18173C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562775 | ||||||
| chr4:83562791
|
G | GAGAT | 5 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+18191_208+1819 others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562791 | |||||
| chr4:83562795
|
T | TATAG | 36 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0332others(33): Show | 36 | HG00099.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.208+18215_208+1821 others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562795 | |||||
| chr4:83562795
|
T | TATAGACA others(13): Show |
5 | a0001c0001t0005g0197a0001c0001t0006g0208a0001c0001t0007g0009others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+18198_208+1819 others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562795 | |||||
| chr4:83562795
|
T | TATAGATA others(1): Show |
64 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.208+18211_208+1821 others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562795 | |||||
| chr4:83562795
|
T | TATAGATA others(5): Show |
2 | a0001c0001t0003g0017a0001c0001t0003g0322 | 2 | HG04184.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.208+18207_208+1821 others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562795 | |||||
| chr4:83562795
|
T | TATAGATA others(9): Show |
1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+18203_208+1821 others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562795 | |||||
| chr4:83562877
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.208+18275G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562877 | ||||||
| chr4:83562881
|
G | T | 3 | a0001c0001t0007g0009a0001c0001t0007g0204a0001c0001t0007g0205 | 3 | HG02622.hp2 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.208+18279G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562881 | ||||||
| chr4:83562963
|
G | A | 76 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.208+18361G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562963 | ||||||
| chr4:83562967
|
T | G | 76 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.208+18365T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562967 | ||||||
| chr4:83563180
|
G | A | 76 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.209-18382G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563180 | ||||||
| chr4:83563478
|
C | CT | 7 | a0001c0001t0001g0077a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG00438.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-18063dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83563478 | |||||
| chr4:83563478
|
CT | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.209-18063delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83563478 | |||||
| chr4:83563478
|
CTT | C | 7 | a0001c0001t0003g0068a0001c0001t0003g0149a0001c0001t0003g0176others(4): Show | 7 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-18064_209-1806 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83563478 | |||||
| chr4:83563481
|
T | C | 7 | a0001c0001t0003g0014a0001c0001t0003g0193a0001c0001t0005g0005others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-18081T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563481 | ||||||
| chr4:83563696
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.209-17866G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563696 | ||||||
| chr4:83563728
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.209-17834G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563728 | ||||||
| chr4:83563773
|
A | G | 76 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.209-17789A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563773 | ||||||
| chr4:83563841
|
T | G | 1 | a0001c0001t0001g0133 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.209-17721T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563841 | ||||||
| chr4:83564062
|
G | A | 5 | a0001c0001t0005g0197a0001c0001t0006g0208a0001c0001t0007g0009others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-17500G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564062 | ||||||
| chr4:83564247
|
G | A | 28 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(25): Show | 28 | HG00099.hp1 HG01243.hp1 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.209-17315G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564247 | ||||||
| chr4:83564374
|
C | T | 18 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-17188C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564374 | ||||||
| chr4:83564469
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.209-17093C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564469 | ||||||
| chr4:83564537
|
A | G | 10 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(7): Show | 10 | HG00099.hp1 HG02486.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-17025A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564537 | ||||||
| chr4:83564557
|
G | A | 2 | a0001c0001t0006g0001a0001c0001t0006g0002 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.209-17005G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564557 | ||||||
| chr4:83564596
|
A | G | 18 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-16966A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564596 | ||||||
| chr4:83564655
|
C | T | 18 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-16907C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564655 | ||||||
| chr4:83564685
|
C | A | 82 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0045others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.209-16877C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564685 | ||||||
| chr4:83564706
|
G | GA | 18 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-16847dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83564706 | |||||
| chr4:83564866
|
T | A | 1 | a0001c0001t0003g0239 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.209-16696T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564866 | ||||||
| chr4:83564878
|
A | AT | 18 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-16676dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83564878 | |||||
| chr4:83564967
|
A | G | 7 | a0001c0001t0003g0196a0001c0001t0004g0198a0001c0001t0004g0199others(4): Show | 7 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-16595A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564967 | ||||||
| chr4:83565011
|
C | T | 71 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-16551C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565011 | ||||||
| chr4:83565012
|
G | A | 3 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0207 | 3 | HG01891.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.209-16550G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565012 | ||||||
| chr4:83565161
|
C | T | 14 | a0001c0001t0001g0077a0001c0001t0002g0213a0001c0001t0002g0214others(11): Show | 14 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.209-16401C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565161 | ||||||
| chr4:83565213
|
G | T | 1 | a0001c0001t0004g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.209-16349G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565213 | ||||||
| chr4:83565341
|
T | A | 1 | a0001c0001t0002g0316 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.209-16221T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565341 | ||||||
| chr4:83565479
|
A | G | 3 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0207 | 3 | HG01891.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.209-16083A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565479 | ||||||
| chr4:83565495
|
AT | A | 97 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.209-16058delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83565495 | |||||
| chr4:83565530
|
G | A | 97 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.209-16032G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565530 | ||||||
| chr4:83565585
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.209-15977G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565585 | ||||||
| chr4:83565685
|
C | T | 3 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215 | 3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.209-15877C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565685 | ||||||
| chr4:83565705
|
C | T | 2 | a0001c0001t0003g0014a0001c0001t0005g0005 | 2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.209-15857C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565705 | ||||||
| chr4:83565715
|
G | A | 89 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.209-15847G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565715 | ||||||
| chr4:83565776
|
C | T | 71 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-15786C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565776 | ||||||
| chr4:83565782
|
G | A | 28 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(25): Show | 28 | HG00099.hp1 HG01243.hp1 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.209-15780G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565782 | ||||||
| chr4:83565936
|
G | A | 2 | a0002c0002t0003g0167a0002c0002t0003g0168 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.209-15626G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565936 | ||||||
| chr4:83565951
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.209-15611C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565951 | ||||||
| chr4:83566066
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.209-15496C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566066 | ||||||
| chr4:83566217
|
T | C | 2 | a0001c0001t0002g0332a0001c0001t0006g0207 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.209-15345T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566217 | ||||||
| chr4:83566264
|
C | G | 1 | a0001c0001t0003g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.209-15298C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566264 | ||||||
| chr4:83566308
|
G | A | 1 | a0001c0001t0005g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.209-15254G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566308 | ||||||
| chr4:83566393
|
A | C | 1 | a0001c0001t0002g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.209-15169A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566393 | ||||||
| chr4:83566404
|
T | A | 113 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.209-15158T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566404 | ||||||
| chr4:83566408
|
AAATT | A | 3 | a0001c0001t0007g0009a0001c0001t0007g0204a0001c0001t0007g0205 | 3 | HG02622.hp2 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.209-15145_209-1514 others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566408 | |||||
| chr4:83566419
|
T | TTTA | 116 | a0001c0001t0001g0072a0001c0001t0001g0083a0001c0001t0001g0084others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.209-15116_209-1511 others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566419 | |||||
| chr4:83566419
|
T | TTTATTA | 65 | a0001c0001t0001g0153a0001c0001t0003g0010a0001c0001t0003g0011others(62): Show | 65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.209-15119_209-1511 others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566419 | |||||
| chr4:83566419
|
T | TTTATTAT others(2): Show |
15 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(12): Show | 15 | HG00099.hp1 HG01243.hp1 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.209-15122_209-1511 others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566419 | |||||
| chr4:83566419
|
T | TTTATTAT others(5): Show |
4 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0310others(1): Show | 4 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-15125_209-1511 others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566419 | |||||
| chr4:83566419
|
T | TTTATTAT others(8): Show |
9 | a0001c0001t0004g0187a0001c0001t0004g0215a0001c0001t0005g0179others(6): Show | 9 | HG02630.hp2 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-15128_209-1511 others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566419 | |||||
| chr4:83566970
|
T | C | 99 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.209-14592T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566970 | ||||||
| chr4:83567146
|
AT | A | 13 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0187others(10): Show | 13 | HG01243.hp1 HG02630.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-14408delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83567146 | |||||
| chr4:83567229
|
T | C | 95 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.209-14333T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83567229 | ||||||
| chr4:83567370
|
G | A | 24 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(21): Show | 24 | HG00099.hp1 HG01243.hp1 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.209-14192G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83567370 | ||||||
| chr4:83567531
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.209-14031G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83567531 | ||||||
| chr4:83567818
|
G | A | 1 | a0001c0001t0004g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.209-13744G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83567818 | ||||||
| chr4:83567969
|
C | T | 95 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.209-13593C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83567969 | ||||||
| chr4:83568316
|
A | G | 4 | a0001c0001t0003g0014a0001c0001t0003g0193a0001c0001t0004g0310others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-13246A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568316 | ||||||
| chr4:83568318
|
G | A | 6 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-13244G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568318 | ||||||
| chr4:83568358
|
G | A | 1 | a0001c0001t0004g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.209-13204G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568358 | ||||||
| chr4:83568364
|
C | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0108 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.209-13198C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568364 | ||||||
| chr4:83568493
|
C | T | 95 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.209-13069C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568493 | ||||||
| chr4:83568510
|
CT | C | 26 | a0001c0001t0001g0074a0001c0001t0002g0183a0001c0001t0002g0189others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.209-13037delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83568510 | |||||
| chr4:83568569
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.209-12993G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568569 | ||||||
| chr4:83568594
|
G | C | 1 | a0001c0001t0002g0250 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.209-12968G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568594 | ||||||
| chr4:83568634
|
G | A | 93 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.209-12928G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568634 | ||||||
| chr4:83568639
|
C | G | 1 | a0001c0001t0001g0097 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.209-12923C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568639 | ||||||
| chr4:83568653
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.209-12909A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568653 | ||||||
| chr4:83569037
|
C | A | 81 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.209-12525C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569037 | ||||||
| chr4:83569195
|
A | G | 71 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-12367A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569195 | ||||||
| chr4:83569371
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.209-12191G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569371 | ||||||
| chr4:83569519
|
G | T | 333 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0045others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.209-12043G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569519 | ||||||
| chr4:83569544
|
ATGTC | A | 71 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-12017_209-1201 others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569544 | ||||||
| chr4:83569555
|
G | A | 71 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-12007G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569555 | ||||||
| chr4:83569586
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.209-11976A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569586 | ||||||
| chr4:83569670
|
G | A | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.209-11892G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569670 | ||||||
| chr4:83569838
|
T | TA | 7 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-11714dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83569838 | |||||
| chr4:83569859
|
T | A | 81 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.209-11703T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569859 | ||||||
| chr4:83569887
|
C | T | 8 | a0001c0001t0005g0197a0001c0001t0006g0001a0001c0001t0006g0002others(5): Show | 8 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-11675C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569887 | ||||||
| chr4:83569968
|
A | C | 116 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.209-11594A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569968 | ||||||
| chr4:83570154
|
C | T | 71 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-11408C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570154 | ||||||
| chr4:83570265
|
T | G | 9 | a0001c0001t0002g0332a0001c0001t0005g0197a0001c0001t0006g0001others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-11297T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570265 | ||||||
| chr4:83570471
|
C | CT | 34 | a0001c0001t0001g0131a0001c0001t0001g0160a0001c0001t0001g0172others(31): Show | 34 | HG01243.hp1 HG02055.hp1 HG02071.hp2 others(31): Show |
intron_variant | MODIFIER | c.209-11072dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83570471 | |||||
| chr4:83570471
|
CT | C | 78 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.209-11072delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83570471 | |||||
| chr4:83570527
|
C | G | 9 | a0001c0001t0002g0332a0001c0001t0005g0197a0001c0001t0006g0001others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-11035C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570527 | ||||||
| chr4:83570563
|
C | A | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-10999C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570563 | ||||||
| chr4:83570621
|
C | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0078others(3): Show | 6 | HG02698.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-10941C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570621 | ||||||
| chr4:83570910
|
A | G | 1 | a0001c0001t0005g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.209-10652A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570910 | ||||||
| chr4:83570967
|
C | A | 17 | a0001c0001t0002g0222a0001c0001t0004g0187a0001c0001t0004g0307others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.209-10595C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570967 | ||||||
| chr4:83571061
|
T | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0206a0001c0001t0005g0219 | 3 | HG00099.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.209-10501T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571061 | ||||||
| chr4:83571438
|
CT | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-10120delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83571438 | |||||
| chr4:83571458
|
T | TTTGTGGG others(7): Show |
1 | a0001c0001t0001g0044 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.209-10102_209-1008 others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83571458 | |||||
| chr4:83571506
|
TAAGTATT others(22): Show |
T | 1 | a0001c0001t0001g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.209-10053_209-1002 others(33): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83571506 | |||||
| chr4:83571585
|
A | T | 1 | a0001c0001t0001g0145 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-9977A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571585 | ||||||
| chr4:83571680
|
A | G | 5 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-9882A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571680 | ||||||
| chr4:83571687
|
TATATATA others(13): Show |
T | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9865_209-9846d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83571687 | |||||
| chr4:83571715
|
T | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9847T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571715 | ||||||
| chr4:83571719
|
C | CACACATA others(35): Show |
1 | a0001c0001t0001g0165 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209-9831_209-9790d others(44): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83571719 | |||||
| chr4:83571725
|
T | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9837T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571725 | ||||||
| chr4:83571739
|
C | T | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.209-9823C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571739 | ||||||
| chr4:83571740
|
G | A | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9822G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571740 | ||||||
| chr4:83571768
|
A | G | 2 | a0001c0001t0002g0039a0001c0001t0002g0266 | 2 | NA18612.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.209-9794A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571768 | ||||||
| chr4:83571901
|
T | A | 1 | a0001c0001t0002g0265 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.209-9661T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571901 | ||||||
| chr4:83571922
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.209-9640G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571922 | ||||||
| chr4:83571952
|
T | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9610T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571952 | ||||||
| chr4:83571973
|
A | G | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9589A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571973 | ||||||
| chr4:83572051
|
A | T | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209-9511A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572051 | ||||||
| chr4:83572160
|
A | G | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9402A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572160 | ||||||
| chr4:83572469
|
C | T | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9093C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572469 | ||||||
| chr4:83572475
|
T | G | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9087T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572475 | ||||||
| chr4:83572477
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9085C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572477 | ||||||
| chr4:83572478
|
T | G | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9084T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572478 | ||||||
| chr4:83572479
|
T | C | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9083T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572479 | ||||||
| chr4:83572485
|
T | G | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9077T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572485 | ||||||
| chr4:83572487
|
A | T | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9075A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572487 | ||||||
| chr4:83572490
|
T | G | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9072T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572490 | ||||||
| chr4:83572498
|
T | G | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9064T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572498 | ||||||
| chr4:83572513
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9049C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572513 | ||||||
| chr4:83572514
|
A | C | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9048A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572514 | ||||||
| chr4:83572518
|
A | T | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9044A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572518 | ||||||
| chr4:83572533
|
A | C | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209-9029A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572533 | ||||||
| chr4:83572845
|
C | T | 13 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0003g0196others(10): Show | 13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-8717C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572845 | ||||||
| chr4:83572846
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.209-8716G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572846 | ||||||
| chr4:83573012
|
CAT | C | 7 | a0001c0001t0001g0120a0001c0001t0002g0209a0001c0001t0002g0210others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-8547_209-8546d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83573012 | |||||
| chr4:83573080
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.209-8482G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83573080 | ||||||
| chr4:83573169
|
C | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0123others(2): Show | 5 | HG02451.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-8393C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83573169 | ||||||
| chr4:83573284
|
GCTTGCCA others(7): Show |
G | 1 | a0001c0001t0001g0163 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.209-8277_209-8264d others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83573284 | ||||||
| chr4:83573773
|
T | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-7789T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83573773 | ||||||
| chr4:83574220
|
G | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-7342G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574220 | ||||||
| chr4:83574366
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.209-7196T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574366 | ||||||
| chr4:83574484
|
G | A | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209-7078G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574484 | ||||||
| chr4:83574489
|
T | C | 87 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.209-7073T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574489 | ||||||
| chr4:83574496
|
T | TAGAG | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-7063_209-7062i others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574496 | |||||
| chr4:83574574
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.209-6988C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574574 | ||||||
| chr4:83574603
|
C | G | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-6959C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574603 | ||||||
| chr4:83574624
|
A | AT | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0103others(6): Show | 9 | HG02071.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-6885dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
A | ATT | 13 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0001g0139others(10): Show | 13 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-6886_209-6885d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
A | ATTT | 6 | a0001c0001t0001g0069a0001c0001t0001g0138a0001c0001t0003g0046others(3): Show | 6 | HG02602.hp2 HG02895.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-6887_209-6885d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.209-6897_209-6885d others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0002g0329 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.209-6902_209-6885d others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
AT | A | 9 | a0001c0001t0001g0070a0001c0001t0001g0120a0001c0001t0002g0209others(6): Show | 9 | HG01884.hp2 HG02809.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-6885delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATT | A | 13 | a0001c0001t0001g0126a0001c0001t0001g0153a0001c0001t0003g0017others(10): Show | 13 | HG00609.hp1 HG01109.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-6886_209-6885d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTT | A | 13 | a0001c0001t0001g0061a0001c0001t0003g0010a0001c0001t0003g0013others(10): Show | 13 | HG00280.hp2 HG02004.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-6887_209-6885d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0134a0001c0001t0001g0165 | 2 | HG02257.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.209-6894_209-6885d others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0001g0094a0001c0001t0001g0308a0001c0001t0002g0280others(1): Show | 4 | HG01261.hp2 HG03927.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-6895_209-6885d others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0045a0001c0001t0004g0307 | 2 | HG01243.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.209-6896_209-6885d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(6): Show |
A | 9 | a0001c0001t0001g0037a0001c0001t0001g0092a0001c0001t0001g0106others(6): Show | 9 | HG01169.hp1 HG01433.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-6897_209-6885d others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(7): Show |
A | 10 | a0001c0001t0001g0067a0001c0001t0001g0091a0001c0001t0001g0098others(7): Show | 10 | HG01168.hp1 HG02071.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-6898_209-6885d others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(8): Show |
A | 12 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0089others(9): Show | 12 | HG00741.hp2 HG02109.hp2 HG03209.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-6899_209-6885d others(17): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(9): Show |
A | 10 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0088others(7): Show | 10 | HG00597.hp2 HG01515.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-6900_209-6885d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(10): Show |
A | 12 | a0001c0001t0001g0066a0001c0001t0001g0078a0001c0001t0001g0087others(9): Show | 12 | HG02486.hp2 HG02970.hp2 HG03492.hp2 others(9): Show |
intron_variant | MODIFIER | c.209-6901_209-6885d others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(11): Show |
A | 7 | a0001c0001t0001g0104a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 7 | HG00733.hp1 HG02293.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-6902_209-6885d others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(12): Show |
A | 12 | a0001c0001t0001g0075a0001c0001t0001g0178a0001c0001t0002g0293others(9): Show | 12 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-6903_209-6885d others(21): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(13): Show |
A | 9 | a0001c0001t0001g0133a0001c0001t0002g0317a0001c0001t0003g0062others(6): Show | 9 | HG00140.hp2 HG01168.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-6904_209-6885d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(14): Show |
A | 12 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0003g0056others(9): Show | 12 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.209-6905_209-6885d others(23): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(15): Show |
A | 13 | a0001c0001t0001g0129a0001c0001t0002g0229a0001c0001t0002g0230others(10): Show | 13 | HG01169.hp2 HG02056.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-6906_209-6885d others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(16): Show |
A | 6 | a0001c0001t0001g0086a0001c0001t0002g0232a0001c0001t0002g0253others(3): Show | 6 | HG01257.hp1 HG01981.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-6907_209-6885d others(25): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(17): Show |
A | 7 | a0001c0001t0003g0018a0001c0001t0003g0182a0001c0001t0004g0121others(4): Show | 7 | HG00099.hp1 HG00733.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-6908_209-6885d others(26): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(18): Show |
A | 5 | a0001c0001t0001g0125a0001c0001t0004g0199a0001c0001t0005g0036others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-6909_209-6885d others(27): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(19): Show |
A | 12 | a0001c0001t0002g0079a0001c0001t0002g0332a0001c0001t0004g0198others(9): Show | 12 | HG01106.hp2 HG01243.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-6910_209-6885d others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(20): Show |
A | 9 | a0001c0001t0001g0044a0001c0001t0001g0110a0001c0001t0002g0252others(6): Show | 9 | HG02027.hp2 NA18951.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-6911_209-6885d others(29): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(21): Show |
A | 46 | a0001c0001t0001g0076a0001c0001t0001g0085a0001c0001t0001g0237others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.209-6912_209-6885d others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(22): Show |
A | 8 | a0001c0001t0001g0174a0001c0001t0001g0242a0001c0001t0002g0260others(5): Show | 8 | HG01256.hp2 NA18939.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-6913_209-6885d others(31): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(23): Show |
A | 3 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0002g0281 | 3 | HG01081.hp1 HG02015.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.209-6914_209-6885d others(32): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(24): Show |
A | 13 | a0001c0001t0001g0152a0001c0001t0001g0156a0001c0001t0001g0157others(10): Show | 13 | HG02055.hp1 HG02809.hp1 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-6915_209-6885d others(33): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(25): Show |
A | 9 | a0001c0001t0001g0142a0001c0001t0001g0154a0001c0001t0001g0159others(6): Show | 9 | HG00438.hp1 HG00609.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-6916_209-6885d others(34): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574624
|
ATTTTTTT others(26): Show |
A | 2 | a0001c0001t0002g0326a0001c0001t0008g0173 | 2 | NA18956.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.209-6917_209-6885d others(35): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | |||||
| chr4:83574665
|
TTTTTTTT others(6): Show |
T | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.209-6896_209-6884d others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574665 | ||||||
| chr4:83574779
|
G | A | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-6783G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574779 | ||||||
| chr4:83574880
|
T | G | 1 | a0001c0001t0001g0145 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6682T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574880 | ||||||
| chr4:83574881
|
T | G | 16 | a0001c0001t0002g0222a0001c0001t0004g0187a0001c0001t0004g0307others(13): Show | 16 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-6681T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574881 | ||||||
| chr4:83574881
|
T | TTG | 69 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.209-6681_209-6680i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574881 | ||||||
| chr4:83574882
|
G | GT | 22 | a0001c0001t0001g0087a0001c0001t0001g0099a0001c0001t0001g0129others(19): Show | 22 | HG00099.hp1 HG00639.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.209-6667dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574882 | |||||
| chr4:83574882
|
G | T | 90 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.209-6680G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574882 | ||||||
| chr4:83574944
|
C | T | 5 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-6618C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574944 | ||||||
| chr4:83575065
|
G | A | 1 | a0001c0001t0002g0317 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.209-6497G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575065 | ||||||
| chr4:83575129
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6433G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575129 | ||||||
| chr4:83575130
|
C | A | 1 | a0001c0001t0001g0145 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6432C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575130 | ||||||
| chr4:83575131
|
C | G | 1 | a0001c0001t0001g0145 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6431C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575131 | ||||||
| chr4:83575132
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6430T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575132 | ||||||
| chr4:83575133
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6429C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575133 | ||||||
| chr4:83575191
|
A | G | 91 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.209-6371A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575191 | ||||||
| chr4:83575511
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.209-6051C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575511 | ||||||
| chr4:83575517
|
A | G | 1 | a0001c0001t0002g0253 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.209-6045A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575517 | ||||||
| chr4:83575700
|
C | T | 8 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(5): Show | 8 | HG02258.hp2 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-5862C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575700 | ||||||
| chr4:83575998
|
C | A | 11 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-5564C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575998 | ||||||
| chr4:83576323
|
G | A | 3 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215 | 3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.209-5239G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83576323 | ||||||
| chr4:83576412
|
T | TTTTA | 131 | a0001c0001t0001g0037a0001c0001t0001g0045a0001c0001t0001g0048others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.209-5109_209-5106d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83576412 | |||||
| chr4:83576412
|
T | TTTTATTT others(1): Show |
19 | a0001c0001t0001g0142a0001c0001t0002g0185a0001c0001t0002g0213others(16): Show | 19 | HG01070.hp2 HG01891.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.209-5113_209-5106d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83576412 | |||||
| chr4:83576412
|
TTTTA | T | 14 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0084others(11): Show | 14 | HG00140.hp2 HG00280.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.209-5109_209-5106d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83576412 | |||||
| chr4:83576412
|
TTTTATTT others(5): Show |
T | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209-5117_209-5106d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83576412 | |||||
| chr4:83576471
|
T | A | 1 | a0001c0001t0007g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.209-5091T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83576471 | ||||||
| chr4:83576472
|
C | T | 1 | a0001c0001t0007g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.209-5090C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83576472 | ||||||
| chr4:83576766
|
A | T | 1 | a0001c0001t0001g0240 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.209-4796A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83576766 | ||||||
| chr4:83576896
|
G | C | 1 | a0001c0001t0002g0211 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.209-4666G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83576896 | ||||||
| chr4:83577010
|
T | G | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209-4552T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577010 | ||||||
| chr4:83577066
|
T | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-4496T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577066 | ||||||
| chr4:83577195
|
T | A | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-4367T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577195 | ||||||
| chr4:83577205
|
G | GAAAGACA others(317): Show |
3 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012 | 3 | NA18612.hp1 NA18969.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.209-4346_209-4345i others(326): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577205 | |||||
| chr4:83577441
|
A | G | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-4121A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577441 | ||||||
| chr4:83577788
|
C | CT | 59 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0075others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.209-3748dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | |||||
| chr4:83577788
|
C | CTT | 13 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0002g0213others(10): Show | 13 | HG00408.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-3749_209-3748d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | |||||
| chr4:83577788
|
C | CTTT | 55 | a0001c0001t0001g0037a0001c0001t0001g0045a0001c0001t0001g0048others(52): Show | 55 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.209-3750_209-3748d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | |||||
| chr4:83577788
|
C | CTTTT | 17 | a0001c0001t0003g0016a0001c0001t0003g0018a0001c0001t0003g0019others(14): Show | 17 | HG00280.hp2 HG00642.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.209-3751_209-3748d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | |||||
| chr4:83577788
|
C | CTTTTT | 6 | a0001c0001t0003g0011a0001c0001t0003g0026a0001c0001t0003g0144others(3): Show | 6 | HG01258.hp2 HG03831.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-3752_209-3748d others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | |||||
| chr4:83577788
|
CT | C | 6 | a0001c0001t0001g0078a0001c0001t0001g0118a0001c0001t0002g0209others(3): Show | 6 | HG01081.hp1 HG02897.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-3748delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | |||||
| chr4:83577937
|
TTACAGGC others(53): Show |
T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-3624_209-3565d others(62): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577937 | ||||||
| chr4:83577951
|
C | T | 13 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0003g0196others(10): Show | 13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-3611C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577951 | ||||||
| chr4:83577976
|
T | C | 20 | a0001c0001t0002g0222a0001c0001t0003g0014a0001c0001t0003g0193others(17): Show | 20 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.209-3586T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577976 | ||||||
| chr4:83578231
|
T | C | 3 | a0001c0001t0003g0071a0001c0001t0003g0144a0001c0001t0003g0212 | 3 | HG00280.hp2 HG01081.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.209-3331T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578231 | ||||||
| chr4:83578376
|
T | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.209-3186T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578376 | ||||||
| chr4:83578829
|
A | C | 3 | a0001c0001t0004g0041a0001c0001t0004g0042a0001c0001t0004g0043 | 3 | HG02145.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.209-2733A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578829 | ||||||
| chr4:83578857
|
T | TTTCC | 76 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.209-2688_209-2685d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578857 | |||||
| chr4:83578857
|
T | TTTCCTTC others(1): Show |
9 | a0001c0001t0003g0014a0001c0001t0003g0193a0001c0001t0005g0006others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2692_209-2685d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578857 | |||||
| chr4:83578921
|
T | C | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2641T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578921 | ||||||
| chr4:83578922
|
T | TTTCTTTC others(4): Show |
58 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0153others(55): Show | 58 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.209-2637_209-2627d others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578922 | |||||
| chr4:83578930
|
T | TTTC | 16 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0003g0011others(13): Show | 16 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-2629_209-2627d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578930 | |||||
| chr4:83578933
|
C | CT | 3 | a0001c0001t0001g0078a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.209-2626dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578933 | |||||
| chr4:83578933
|
CTTTCT | C | 7 | a0001c0001t0004g0041a0001c0001t0004g0121a0001c0001t0004g0200others(4): Show | 7 | HG02055.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-2611_209-2607d others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578933 | |||||
| chr4:83578937
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.209-2625C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578937 | ||||||
| chr4:83578937
|
CT | C | 3 | a0001c0001t0005g0191a0001c0001t0005g0220a0001c0001t0005g0224 | 3 | HG03139.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.209-2621delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578937 | |||||
| chr4:83578938
|
T | TTTC | 16 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0003g0011others(13): Show | 16 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-2622_209-2621i others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578938 | |||||
| chr4:83578939
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.209-2623T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578939 | ||||||
| chr4:83578942
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.209-2620C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578942 | ||||||
| chr4:83578943
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0002g0314 | 2 | NA18952.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.209-2619T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578943 | ||||||
| chr4:83578943
|
T | TTCTTTCT others(3): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0178 | 2 | HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.209-2618_209-2617i others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578943 | |||||
| chr4:83578943
|
T | TTTCTTTC others(4): Show |
3 | a0001c0001t0001g0078a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.209-2617_209-2616i others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578943 | |||||
| chr4:83578943
|
TTTTCTTT others(68): Show |
T | 1 | a0001c0001t0005g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.209-2611_209-2537d others(77): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578943 | |||||
| chr4:83578943
|
TTTTCTTT others(76): Show |
T | 1 | a0001c0001t0009g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.209-2611_209-2529d others(85): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578943 | |||||
| chr4:83578946
|
TCTTTTCT others(64): Show |
T | 1 | a0001c0001t0009g0007 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.209-2611_209-2541d others(73): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578946 | |||||
| chr4:83578947
|
CT | C | 23 | a0001c0001t0001g0075a0001c0001t0001g0081a0001c0001t0001g0098others(20): Show | 23 | HG01243.hp1 HG01243.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.209-2611delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578947 | |||||
| chr4:83578947
|
CTTT | C | 13 | a0001c0001t0001g0308a0001c0001t0002g0210a0001c0001t0002g0229others(10): Show | 13 | HG02258.hp2 HG02559.hp2 HG02970.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-2613_209-2611d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578947 | |||||
| chr4:83578947
|
CTTTTCTT | C | 3 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0234 | 3 | HG02622.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.209-2613_209-2607d others(9): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578947 | |||||
| chr4:83578947
|
CTTTTCTT others(4): Show |
C | 1 | a0001c0001t0002g0232 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.209-2613_209-2603d others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578947 | |||||
| chr4:83578948
|
T | TC | 99 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0133others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.209-2614_209-2613i others(3): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | ||||||
| chr4:83578948
|
T | TCTTTC | 25 | a0001c0001t0002g0025a0001c0001t0002g0112a0001c0001t0002g0184others(22): Show | 25 | HG01168.hp2 HG01192.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.209-2614_209-2613i others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | ||||||
| chr4:83578948
|
T | TCTTTCTT others(2): Show |
24 | a0001c0001t0002g0015a0001c0001t0002g0183a0001c0001t0002g0189others(21): Show | 24 | HG00408.hp1 HG00438.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.209-2614_209-2613i others(11): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | ||||||
| chr4:83578948
|
T | TCTTTCTT others(6): Show |
6 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0003g0033others(3): Show | 6 | HG00597.hp1 HG02015.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2614_209-2613i others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | ||||||
| chr4:83578948
|
T | TCTTTCTT others(10): Show |
1 | a0001c0001t0003g0022 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.209-2614_209-2613i others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | ||||||
| chr4:83578948
|
T | TCTTTCTT others(22): Show |
1 | a0001c0001t0003g0114 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.209-2614_209-2613i others(31): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | ||||||
| chr4:83578948
|
T | TTCTTTCT others(19): Show |
1 | a0001c0001t0003g0030 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.209-2613_209-2612i others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | |||||
| chr4:83578948
|
T | TTTC | 30 | a0001c0001t0001g0037a0001c0001t0001g0045a0001c0001t0001g0069others(27): Show | 30 | HG00609.hp2 HG00741.hp2 HG01515.hp2 others(27): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | |||||
| chr4:83578948
|
T | TTTCTTTC | 14 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0094others(11): Show | 14 | HG00597.hp2 HG01106.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(9): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | |||||
| chr4:83578948
|
T | TTTCTTTC others(4): Show |
12 | a0001c0001t0001g0067a0001c0001t0001g0096a0001c0001t0001g0102others(9): Show | 12 | HG01168.hp1 HG01175.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | |||||
| chr4:83578948
|
T | TTTCTTTC others(8): Show |
16 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0082others(13): Show | 16 | HG00408.hp2 HG01346.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(17): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | |||||
| chr4:83578948
|
T | TTTCTTTC others(12): Show |
17 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0087others(14): Show | 17 | HG01081.hp1 HG01261.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(21): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | |||||
| chr4:83578948
|
T | TTTCTTTC others(16): Show |
8 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0089others(5): Show | 8 | HG00438.hp1 HG02523.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(25): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | |||||
| chr4:83578948
|
T | TTTCTTTC others(20): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0108a0001c0001t0001g0160 | 3 | HG01169.hp1 NA18972.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.209-2612_209-2611i others(29): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | |||||
| chr4:83578948
|
T | TTTCTTTC others(28): Show |
1 | a0001c0001t0001g0099 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.209-2612_209-2611i others(37): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | |||||
| chr4:83578949
|
T | C | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-2613T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578949 | ||||||
| chr4:83578950
|
T | TTC | 11 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0003g0011others(8): Show | 11 | HG00642.hp1 HG01070.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-2610_209-2609d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578950 | |||||
| chr4:83578950
|
TTCTTTCT others(60): Show |
T | 2 | a0001c0001t0005g0005a0001c0001t0005g0206 | 2 | HG00099.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.209-2611_209-2545d others(69): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578950 | ||||||
| chr4:83578952
|
CTT | C | 5 | a0001c0001t0003g0014a0001c0001t0003g0023a0001c0001t0003g0024others(2): Show | 5 | HG00280.hp2 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2608_209-2607d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578952 | |||||
| chr4:83578958
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.209-2604T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578958 | ||||||
| chr4:83578963
|
T | G | 5 | a0001c0001t0005g0197a0001c0001t0006g0001a0001c0001t0006g0002others(2): Show | 5 | HG01891.hp1 HG02572.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2599T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578963 | ||||||
| chr4:83578963
|
T | TCTTGCTT others(51): Show |
3 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215 | 3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.209-2596_209-2595i others(60): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578963 | |||||
| chr4:83578967
|
T | G | 1 | a0001c0001t0003g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.209-2595T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578967 | ||||||
| chr4:83578971
|
T | G | 5 | a0001c0001t0002g0332a0001c0001t0005g0036a0001c0001t0006g0208others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-2591T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578971 | ||||||
| chr4:83578978
|
T | A | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2584T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578978 | ||||||
| chr4:83578985
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0139 | 2 | HG01081.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.209-2577T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578985 | ||||||
| chr4:83578987
|
TCCTTCCT others(23): Show |
T | 3 | a0001c0001t0002g0222a0001c0001t0005g0220a0001c0001t0005g0224 | 3 | HG02559.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.209-2573_209-2544d others(32): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578987 | |||||
| chr4:83578989
|
C | T | 193 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0070others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.209-2573C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578989 | ||||||
| chr4:83578991
|
TCCTTCCT others(19): Show |
T | 1 | a0001c0001t0005g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.209-2569_209-2544d others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578991 | |||||
| chr4:83578992
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2570C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578992 | ||||||
| chr4:83578993
|
C | T | 126 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0070others(123): Show | 126 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.209-2569C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578993 | ||||||
| chr4:83578995
|
TCCTTCCT others(15): Show |
T | 7 | a0001c0001t0002g0248a0001c0001t0002g0257a0001c0001t0002g0258others(4): Show | 7 | HG02004.hp2 HG02451.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-2565_209-2544d others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578995 | |||||
| chr4:83578996
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2566C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578996 | ||||||
| chr4:83578997
|
C | T | 96 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0070others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.209-2565C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578997 | ||||||
| chr4:83579000
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2562C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579000 | ||||||
| chr4:83579001
|
C | T | 55 | a0001c0001t0001g0070a0001c0001t0001g0122a0001c0001t0001g0133others(52): Show | 55 | HG00639.hp1 HG00642.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.209-2561C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579001 | ||||||
| chr4:83579004
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2558C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579004 | ||||||
| chr4:83579005
|
C | T | 26 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0308others(23): Show | 26 | HG01243.hp1 HG01346.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.209-2557C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579005 | ||||||
| chr4:83579007
|
TCCTTCTT others(3): Show |
T | 1 | a0001c0001t0002g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.209-2553_209-2544d others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579007 | |||||
| chr4:83579008
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2554C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579008 | ||||||
| chr4:83579009
|
C | T | 8 | a0001c0001t0001g0308a0001c0001t0002g0210a0001c0001t0002g0280others(5): Show | 8 | HG01346.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2553C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579009 | ||||||
| chr4:83579009
|
CTTCTTTC others(29): Show |
C | 1 | a0001c0001t0012g0245 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.209-2552_209-2517d others(38): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579009 | ||||||
| chr4:83579009
|
CTTCTTTC others(33): Show |
C | 1 | a0001c0001t0004g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.209-2552_209-2513d others(42): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579009 | ||||||
| chr4:83579009
|
CTTCTTTC others(37): Show |
C | 2 | a0001c0001t0005g0319a0001c0001t0014g0004 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.209-2552_209-2509d others(46): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579009 | ||||||
| chr4:83579012
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2550C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579012 | ||||||
| chr4:83579013
|
T | C | 100 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0070others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.209-2549T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579013 | ||||||
| chr4:83579017
|
C | CCTTT | 9 | a0001c0001t0001g0089a0001c0001t0001g0100a0001c0001t0001g0104others(6): Show | 9 | HG01106.hp2 HG01261.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-2485_209-2482d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579017
|
C | CCTTTCTT others(1): Show |
4 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0001g0142others(1): Show | 4 | HG01891.hp2 NA18944.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-2489_209-2482d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579017
|
C | CCTTTCTT others(5): Show |
3 | a0001c0001t0001g0094a0001c0001t0001g0138a0001c0001t0001g0175 | 3 | HG01175.hp2 HG03927.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.209-2493_209-2482d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579017
|
C | CCTTTCTT others(13): Show |
1 | a0001c0001t0001g0090 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.209-2501_209-2482d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579017
|
C | CTT | 22 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0106others(19): Show | 22 | HG00597.hp2 HG00609.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.209-2545_209-2544i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | ||||||
| chr4:83579017
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2545C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | ||||||
| chr4:83579017
|
CCT | C | 43 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0075others(40): Show | 43 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.209-2544_209-2543d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | ||||||
| chr4:83579017
|
CCTTT | C | 29 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0073others(26): Show | 29 | HG00639.hp2 HG00741.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.209-2485_209-2482d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579017
|
CCTTTCT | C | 6 | a0001c0001t0001g0133a0001c0001t0002g0155a0001c0001t0002g0210others(3): Show | 6 | HG00642.hp2 HG02559.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-2544_209-2539d others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | ||||||
| chr4:83579017
|
CCTTTCTT others(1): Show |
C | 4 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0002g0332others(1): Show | 4 | HG02040.hp2 HG02145.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-2489_209-2482d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579017
|
CCTTTCTT others(3): Show |
C | 6 | a0001c0001t0002g0253a0001c0001t0002g0262a0001c0001t0002g0265others(3): Show | 6 | HG00733.hp1 HG01257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2544_209-2535d others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | ||||||
| chr4:83579017
|
CCTTTCTT others(5): Show |
C | 1 | a0001c0001t0004g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2493_209-2482d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579017
|
CCTTTCTT others(7): Show |
C | 8 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0002g0039others(5): Show | 8 | HG01884.hp1 HG02145.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2544_209-2531d others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | ||||||
| chr4:83579017
|
CCTTTCTT others(9): Show |
C | 1 | a0001c0001t0004g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.209-2497_209-2482d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579017
|
CCTTTCTT others(11): Show |
C | 10 | a0001c0001t0001g0243a0001c0001t0002g0185a0001c0001t0002g0209others(7): Show | 10 | HG00099.hp2 HG02717.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-2544_209-2527d others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | ||||||
| chr4:83579017
|
CCTTTCTT others(13): Show |
C | 4 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2501_209-2482d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579017
|
CCTTTCTT others(15): Show |
C | 9 | a0001c0001t0002g0271a0001c0001t0002g0282a0001c0001t0002g0295others(6): Show | 9 | HG01192.hp1 HG02622.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2544_209-2523d others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | ||||||
| chr4:83579017
|
CCTTTCTT others(19): Show |
C | 3 | a0001c0001t0002g0250a0001c0001t0002g0269a0001c0001t0002g0276 | 3 | NA18968.hp2 NA18997.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.209-2544_209-2519d others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | ||||||
| chr4:83579017
|
CCTTTCTT others(25): Show |
C | 3 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0223 | 3 | HG02818.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.209-2513_209-2482d others(34): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579017
|
CCTTTCTT others(29): Show |
C | 1 | a0001c0001t0005g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.209-2517_209-2482d others(38): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | |||||
| chr4:83579019
|
T | C | 23 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0106others(20): Show | 23 | HG00597.hp2 HG00609.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.209-2543T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579019 | ||||||
| chr4:83579021
|
T | C | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2541T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579021 | ||||||
| chr4:83579023
|
T | C | 30 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0109others(27): Show | 30 | HG00639.hp1 HG01070.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-2539T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579023 | ||||||
| chr4:83579025
|
T | TCC | 23 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0098others(20): Show | 23 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.209-2536_209-2535i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579025 | |||||
| chr4:83579026
|
CTT | C | 13 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0159others(10): Show | 13 | HG00140.hp2 HG00642.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-2534_209-2533d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579026 | |||||
| chr4:83579027
|
T | C | 20 | a0001c0001t0001g0070a0001c0001t0001g0122a0001c0001t0001g0133others(17): Show | 20 | HG00642.hp2 HG01070.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.209-2535T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579027 | ||||||
| chr4:83579029
|
T | C | 14 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0159others(11): Show | 14 | HG00140.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.209-2533T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579029 | ||||||
| chr4:83579029
|
T | TCC | 9 | a0001c0001t0001g0069a0001c0001t0001g0109a0001c0001t0001g0110others(6): Show | 9 | HG00639.hp1 HG01496.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2532_209-2531i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579029 | |||||
| chr4:83579030
|
CTT | C | 8 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0244others(5): Show | 8 | HG01106.hp1 HG01109.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-2530_209-2529d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579030 | |||||
| chr4:83579031
|
T | C | 22 | a0001c0001t0001g0133a0001c0001t0001g0308a0001c0001t0002g0155others(19): Show | 22 | HG01257.hp1 HG01346.hp2 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.209-2531T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579031 | ||||||
| chr4:83579033
|
T | C | 9 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0244others(6): Show | 9 | HG01106.hp1 HG01109.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2529T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579033 | ||||||
| chr4:83579033
|
T | TCC | 4 | a0001c0001t0001g0070a0001c0001t0001g0122a0001c0001t0003g0327others(1): Show | 4 | HG04228.hp1 HG06807.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2528_209-2527i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579033 | |||||
| chr4:83579034
|
CTT | C | 6 | a0001c0001t0002g0305a0001c0001t0002g0320a0001c0001t0003g0068others(3): Show | 6 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-2526_209-2525d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579034 | |||||
| chr4:83579035
|
T | C | 29 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0308others(26): Show | 29 | HG01346.hp2 HG01884.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.209-2527T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579035 | ||||||
| chr4:83579037
|
T | C | 7 | a0001c0001t0002g0305a0001c0001t0002g0314a0001c0001t0002g0320others(4): Show | 7 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-2525T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579037 | ||||||
| chr4:83579038
|
CTT | C | 5 | a0001c0001t0001g0133a0001c0001t0002g0155a0001c0001t0002g0253others(2): Show | 5 | HG01257.hp1 HG02615.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-2522_209-2521d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579038 | |||||
| chr4:83579039
|
T | C | 28 | a0001c0001t0002g0039a0001c0001t0002g0185a0001c0001t0002g0209others(25): Show | 28 | HG01346.hp2 HG01884.hp1 HG02004.hp2 others(25): Show |
intron_variant | MODIFIER | c.209-2523T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579039 | ||||||
| chr4:83579041
|
T | C | 7 | a0001c0001t0001g0133a0001c0001t0002g0155a0001c0001t0002g0253others(4): Show | 7 | HG01257.hp1 HG02615.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-2521T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579041 | ||||||
| chr4:83579042
|
CTT | C | 11 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(8): Show | 11 | HG00099.hp2 HG02717.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-2518_209-2517d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579042 | |||||
| chr4:83579043
|
T | C | 20 | a0001c0001t0002g0222a0001c0001t0002g0248a0001c0001t0002g0257others(17): Show | 20 | HG01192.hp1 HG02004.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.209-2519T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579043 | ||||||
| chr4:83579043
|
TTTCTTTC others(33): Show |
T | 1 | a0001c0001t0015g0003 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.209-2515_209-2476d others(42): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579043 | |||||
| chr4:83579045
|
T | C | 61 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.209-2517T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579045 | ||||||
| chr4:83579045
|
T | TCCTTCCT others(194): Show |
1 | a0001c0001t0005g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209-2516_209-2515i others(203): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579045 | |||||
| chr4:83579045
|
TCTTTCTT others(29): Show |
T | 1 | a0001c0001t0005g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.209-2515_209-2480d others(38): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579045 | |||||
| chr4:83579046
|
CTT | C | 18 | a0001c0001t0002g0039a0001c0001t0002g0185a0001c0001t0002g0209others(15): Show | 18 | HG01346.hp2 HG01884.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-2514_209-2513d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579046 | |||||
| chr4:83579047
|
T | C | 16 | a0001c0001t0002g0222a0001c0001t0002g0248a0001c0001t0002g0257others(13): Show | 16 | HG02004.hp2 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-2515T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579047 | ||||||
| chr4:83579047
|
TTTCTTTC others(33): Show |
T | 11 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0189others(8): Show | 11 | HG02258.hp2 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2511_209-2472d others(42): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579047 | |||||
| chr4:83579049
|
T | C | 19 | a0001c0001t0002g0039a0001c0001t0002g0185a0001c0001t0002g0209others(16): Show | 19 | HG01346.hp2 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.209-2513T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579049 | ||||||
| chr4:83579049
|
T | TCCTTCCT others(194): Show |
1 | a0001c0001t0003g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.209-2512_209-2511i others(203): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579049 | |||||
| chr4:83579049
|
TCTTTCTT others(25): Show |
T | 25 | a0001c0001t0002g0015a0001c0001t0002g0112a0001c0001t0002g0183others(22): Show | 25 | HG00408.hp1 HG00438.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.209-2511_209-2480d others(34): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579049 | |||||
| chr4:83579050
|
CTT | C | 11 | a0001c0001t0002g0250a0001c0001t0002g0269a0001c0001t0002g0271others(8): Show | 11 | HG01192.hp1 HG02109.hp1 NA18959.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2510_209-2509d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579050 | |||||
| chr4:83579051
|
T | C | 15 | a0001c0001t0002g0025a0001c0001t0002g0211a0001c0001t0002g0238others(12): Show | 15 | HG01070.hp2 HG01256.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.209-2511T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579051 | ||||||
| chr4:83579053
|
T | C | 11 | a0001c0001t0002g0250a0001c0001t0002g0269a0001c0001t0002g0271others(8): Show | 11 | HG01192.hp1 HG02109.hp1 NA18959.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2509T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579053 | ||||||
| chr4:83579053
|
T | TCC | 11 | a0001c0001t0002g0222a0001c0001t0002g0248a0001c0001t0002g0257others(8): Show | 11 | HG02004.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2508_209-2507i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579053 | |||||
| chr4:83579053
|
T | TCTTTCTT others(190): Show |
1 | a0001c0001t0003g0014 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.209-2500_209-2499i others(199): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579053 | |||||
| chr4:83579053
|
TCTTTCTT others(21): Show |
T | 9 | a0001c0001t0002g0025a0001c0001t0002g0211a0001c0001t0002g0238others(6): Show | 9 | HG01256.hp2 HG01433.hp2 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2507_209-2480d others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579053 | |||||
| chr4:83579055
|
T | C | 6 | a0001c0001t0002g0254a0001c0001t0002g0272a0001c0001t0002g0274others(3): Show | 6 | HG01070.hp2 HG01517.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2507T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579055 | ||||||
| chr4:83579057
|
T | C | 2 | a0001c0001t0002g0293a0001c0001t0006g0208 | 2 | HG00140.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.209-2505T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579057 | ||||||
| chr4:83579057
|
TCTTTCTT others(17): Show |
T | 3 | a0001c0001t0002g0254a0001c0001t0002g0274a0001c0001t0004g0187 | 3 | HG01517.hp1 HG01981.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.209-2503_209-2480d others(26): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579057 | |||||
| chr4:83579059
|
T | C | 4 | a0001c0001t0002g0272a0001c0001t0002g0279a0001c0001t0006g0208others(1): Show | 4 | HG01070.hp2 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2503T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579059 | ||||||
| chr4:83579059
|
TTTCTTTC others(21): Show |
T | 2 | a0001c0001t0003g0010a0001c0001t0003g0034 | 2 | NA18969.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.209-2499_209-2472d others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579059 | |||||
| chr4:83579061
|
T | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0217others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-2501T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579061 | ||||||
| chr4:83579061
|
TCTTTCTT others(13): Show |
T | 2 | a0001c0001t0002g0272a0001c0001t0002g0279 | 2 | HG01070.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.209-2499_209-2480d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579061 | |||||
| chr4:83579063
|
T | C | 4 | a0001c0001t0002g0293a0001c0001t0006g0208a0001c0001t0007g0009others(1): Show | 4 | HG00140.hp1 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2499T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579063 | ||||||
| chr4:83579063
|
TTTCTTTC others(17): Show |
T | 7 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0003g0013others(4): Show | 7 | HG01109.hp1 HG02486.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-2495_209-2472d others(26): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579063 | |||||
| chr4:83579063
|
TTTCTTTC others(21): Show |
T | 1 | a0001c0001t0003g0239 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.209-2495_209-2468d others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579063 | |||||
| chr4:83579063
|
TTTCTTTC others(25): Show |
T | 2 | a0001c0001t0002g0244a0001c0001t0003g0056 | 2 | NA18944.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.209-2495_209-2464d others(34): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579063 | |||||
| chr4:83579065
|
T | C | 8 | a0001c0001t0002g0314a0001c0001t0003g0297a0001c0001t0003g0304others(5): Show | 8 | HG01169.hp2 HG01891.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2497T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579065 | ||||||
| chr4:83579065
|
TCTTTCTT others(9): Show |
T | 1 | a0001c0001t0002g0293 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.209-2495_209-2480d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579065 | |||||
| chr4:83579066
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2496C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579066 | ||||||
| chr4:83579067
|
T | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0006g0208others(2): Show | 5 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2495T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579067 | ||||||
| chr4:83579067
|
T | TTCCCTTC others(5): Show |
1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.209-2494_209-2493i others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579067 | |||||
| chr4:83579067
|
TTTCTTTC others(9): Show |
T | 2 | a0001c0001t0003g0012a0001c0001t0003g0144 | 2 | HG03831.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.209-2491_209-2476d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579067 | |||||
| chr4:83579067
|
TTTCTTTC others(13): Show |
T | 9 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0059others(6): Show | 9 | HG00609.hp1 HG03490.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2491_209-2472d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579067 | |||||
| chr4:83579067
|
TTTCTTTC others(17): Show |
T | 2 | a0001c0001t0003g0050a0001c0001t0003g0289 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.209-2491_209-2468d others(26): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579067 | |||||
| chr4:83579069
|
T | C | 8 | a0001c0001t0002g0155a0001c0001t0002g0253a0001c0001t0002g0314others(5): Show | 8 | HG00099.hp1 HG01257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2493T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579069 | ||||||
| chr4:83579069
|
T | TC | 3 | a0001c0001t0004g0215a0002c0002t0003g0167a0002c0002t0003g0168 | 3 | HG01257.hp2 HG01258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.209-2492dupC | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579069 | |||||
| chr4:83579069
|
T | TCCTTCCT others(6): Show |
1 | a0001c0001t0005g0197 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.209-2492_209-2491i others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579069 | |||||
| chr4:83579069
|
T | TCCTTCCT others(10): Show |
1 | a0001c0001t0006g0207 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.209-2492_209-2491i others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579069 | |||||
| chr4:83579071
|
T | C | 13 | a0001c0001t0001g0074a0001c0001t0001g0118a0001c0001t0002g0213others(10): Show | 13 | HG00099.hp1 HG01081.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-2491T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579071 | ||||||
| chr4:83579071
|
TTTCTTTC others(5): Show |
T | 2 | a0001c0001t0003g0019a0001c0001t0003g0212 | 2 | HG00280.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.209-2487_209-2476d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579071 | |||||
| chr4:83579071
|
TTTCTTTC others(9): Show |
T | 4 | a0001c0001t0001g0049a0001c0001t0003g0027a0001c0001t0003g0060others(1): Show | 4 | HG00280.hp1 HG03834.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2487_209-2472d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579071 | |||||
| chr4:83579071
|
TTTCTTTC others(13): Show |
T | 2 | a0001c0001t0003g0127a0001c0001t0003g0302 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.209-2487_209-2468d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579071 | |||||
| chr4:83579073
|
T | C | 18 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243others(15): Show | 18 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-2489T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579073 | ||||||
| chr4:83579073
|
T | TCCTTCCT others(10): Show |
1 | a0001c0001t0006g0001 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.209-2488_209-2487i others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579073 | |||||
| chr4:83579075
|
T | C | 18 | a0001c0001t0001g0066a0001c0001t0001g0103a0001c0001t0001g0118others(15): Show | 18 | HG00099.hp1 HG01081.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-2487T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579075 | ||||||
| chr4:83579075
|
T | TTTCTTTC others(7): Show |
1 | a0001c0001t0001g0136 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.209-2482_209-2481i others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579075 | |||||
| chr4:83579075
|
TTTCTTCC others(5): Show |
T | 3 | a0001c0001t0003g0016a0001c0001t0003g0052a0001c0001t0003g0064 | 3 | NA19057.hp2 NA19064.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.209-2483_209-2472d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579075 | |||||
| chr4:83579075
|
TTTCTTCC others(9): Show |
T | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-2483_209-2468d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579075 | |||||
| chr4:83579077
|
T | C | 23 | a0001c0001t0001g0133a0001c0001t0002g0039a0001c0001t0002g0216others(20): Show | 23 | HG00642.hp2 HG00733.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.209-2485T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579077 | ||||||
| chr4:83579079
|
T | C | 28 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0001t0001g0240others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.209-2483T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579079 | ||||||
| chr4:83579079
|
TTCCCTTC others(1): Show |
T | 17 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0020others(14): Show | 17 | HG00140.hp2 HG00597.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.209-2481_209-2474d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579079 | |||||
| chr4:83579079
|
TTCCCTTC others(5): Show |
T | 1 | a0001c0001t0003g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.209-2481_209-2470d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579079 | |||||
| chr4:83579081
|
C | CCCTT | 25 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0073others(22): Show | 25 | HG00438.hp1 HG01106.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.209-2436_209-2433d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
C | CCCTTCCT others(1): Show |
10 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0081others(7): Show | 10 | HG01993.hp1 HG02015.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-2440_209-2433d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
C | CCCTTCCT others(5): Show |
6 | a0001c0001t0001g0098a0001c0001t0001g0124a0001c0001t0001g0131others(3): Show | 6 | HG02071.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2444_209-2433d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
C | CCCTTCCT others(9): Show |
4 | a0001c0001t0001g0122a0001c0001t0004g0188a0001c0001t0005g0331others(1): Show | 4 | HG02965.hp2 HG03579.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2448_209-2433d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
C | CCCTTCCT others(13): Show |
1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.209-2452_209-2433d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
C | CCCTTCCT others(17): Show |
1 | a0001c0001t0001g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209-2456_209-2433d others(26): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
C | CCCTTCCT others(21): Show |
1 | a0001c0001t0001g0119 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.209-2460_209-2433d others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
C | CCTT | 7 | a0001c0001t0004g0215a0001c0001t0005g0197a0001c0001t0006g0001others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-2480_209-2479i others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
C | CCTTCCTT others(16): Show |
1 | a0001c0001t0006g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.209-2480_209-2479i others(25): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
C | T | 55 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0001t0001g0133others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.209-2481C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579081 | ||||||
| chr4:83579081
|
CCCTT | C | 24 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0078others(21): Show | 24 | HG00597.hp2 HG00609.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.209-2436_209-2433d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
CCCTTCCT others(1): Show |
C | 8 | a0001c0001t0001g0037a0001c0001t0001g0045a0001c0001t0001g0150others(5): Show | 8 | HG00741.hp2 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2440_209-2433d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579081
|
CCCTTCCT others(5): Show |
C | 1 | a0001c0001t0004g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.209-2444_209-2433d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | |||||
| chr4:83579083
|
C | T | 36 | a0001c0001t0002g0184a0001c0001t0002g0185a0001c0001t0002g0186others(33): Show | 36 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.209-2479C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579083 | ||||||
| chr4:83579085
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0015g0003 | 2 | HG02055.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.209-2477T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579085 | ||||||
| chr4:83579087
|
C | T | 13 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0003g0017others(10): Show | 13 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-2475C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579087 | ||||||
| chr4:83579130
|
T | C | 77 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.209-2432T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579130 | ||||||
| chr4:83579132
|
T | C | 1 | a0001c0001t0002g0280 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.209-2430T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579132 | ||||||
| chr4:83579134
|
T | C | 3 | a0001c0001t0002g0259a0001c0001t0004g0095a0001c0001t0004g0310 | 3 | HG01261.hp2 HG02109.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.209-2428T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579134 | ||||||
| chr4:83579137
|
C | T | 1 | a0001c0001t0004g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2425C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579137 | ||||||
| chr4:83579141
|
C | T | 1 | a0001c0001t0004g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2421C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579141 | ||||||
| chr4:83579146
|
CCT | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-2407_209-2406d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579146 | |||||
| chr4:83579150
|
T | C | 1 | a0001c0001t0004g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2412T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579150 | ||||||
| chr4:83579154
|
T | C | 1 | a0001c0001t0004g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2408T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579154 | ||||||
| chr4:83579157
|
T | C | 1 | a0001c0001t0004g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2405T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579157 | ||||||
| chr4:83579278
|
T | TTCCCC | 5 | a0001c0001t0002g0079a0001c0001t0002g0292a0001c0001t0005g0005others(2): Show | 5 | HG00099.hp1 HG01106.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2260_209-2256d others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579278 | |||||
| chr4:83579278
|
TTCCCC | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG01081.hp1 HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.209-2260_209-2256d others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579278 | |||||
| chr4:83579368
|
C | T | 11 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2194C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579368 | ||||||
| chr4:83579403
|
C | G | 4 | a0001c0001t0003g0040a0001c0001t0003g0054a0001c0001t0003g0055others(1): Show | 4 | NA18946.hp1 NA18964.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2159C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579403 | ||||||
| chr4:83579404
|
T | C | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2158T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579404 | ||||||
| chr4:83579405
|
G | T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2157G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579405 | ||||||
| chr4:83579406
|
C | G | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2156C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579406 | ||||||
| chr4:83579482
|
A | G | 11 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2080A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579482 | ||||||
| chr4:83579848
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.209-1714A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579848 | ||||||
| chr4:83579857
|
C | T | 1 | a0001c0001t0004g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-1705C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579857 | ||||||
| chr4:83580140
|
A | G | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-1422A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580140 | ||||||
| chr4:83580310
|
C | A | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-1252C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580310 | ||||||
| chr4:83580362
|
CTTGA | C | 5 | a0001c0001t0002g0155a0001c0001t0002g0260a0001c0001t0002g0261others(2): Show | 5 | NA18943.hp2 NA18948.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-1197_209-1194d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83580362 | |||||
| chr4:83580572
|
C | T | 1 | a0001c0001t0002g0025 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.209-990C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580572 | ||||||
| chr4:83580810
|
A | G | 109 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.209-752A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580810 | ||||||
| chr4:83580814
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.209-748C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580814 | ||||||
| chr4:83580892
|
T | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-670T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580892 | ||||||
| chr4:83580965
|
G | A | 1 | a0001c0004t0004g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.209-597G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580965 | ||||||
| chr4:83580968
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.209-594T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580968 | ||||||
| chr4:83581025
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.209-537G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83581025 | ||||||
| chr4:83581065
|
C | T | 1 | a0001c0001t0002g0253 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.209-497C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83581065 | ||||||
| chr4:83581095
|
C | CA | 120 | a0001c0001t0001g0044a0001c0001t0001g0075a0001c0001t0001g0076others(117): Show | 120 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.209-441dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83581095 | |||||
| chr4:83581095
|
C | CAA | 46 | a0001c0001t0001g0131a0001c0001t0001g0225a0001c0001t0001g0308others(43): Show | 46 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.209-442_209-441dup others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83581095 | |||||
| chr4:83581095
|
CAAAAAAA | C | 10 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0026others(7): Show | 10 | HG01070.hp1 HG02602.hp2 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-447_209-441del others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83581095 | |||||
| chr4:83581095
|
CAAAAAAA others(1): Show |
C | 63 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.209-448_209-441del others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83581095 | |||||
| chr4:83581218
|
C | T | 1 | a0001c0001t0003g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.209-344C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83581218 | ||||||
| chr4:83581449
|
A | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-113A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83581449 | ||||||
| chr4:83581523
|
C | T | 4 | a0001c0001t0001g0255a0001c0001t0005g0197a0001c0001t0006g0001others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-39C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83581523 | ||||||
| chr4:83581891
|
T | C | 6 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.479+59T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83581891 | ||||||
| chr4:83581972
|
A | G | 233 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.479+140A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83581972 | ||||||
| chr4:83581973
|
A | C | 233 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.479+141A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83581973 | ||||||
| chr4:83582138
|
GGAA | G | 13 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0003g0196others(10): Show | 13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.479+318_479+320del others(3): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83582138 | |||||
| chr4:83582205
|
T | C | 1 | a0001c0001t0003g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.479+373T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582205 | ||||||
| chr4:83582222
|
C | T | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.479+390C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582222 | ||||||
| chr4:83582289
|
C | T | 1 | a0001c0001t0002g0292 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.479+457C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582289 | ||||||
| chr4:83582344
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.479+512G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582344 | ||||||
| chr4:83582352
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.479+520C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582352 | ||||||
| chr4:83582411
|
G | A | 1 | a0001c0001t0003g0057 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.479+579G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582411 | ||||||
| chr4:83582446
|
C | T | 7 | a0001c0001t0001g0092a0001c0001t0004g0198a0001c0001t0004g0199others(4): Show | 7 | HG01243.hp2 HG02055.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.479+614C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582446 | ||||||
| chr4:83582447
|
G | A | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+615G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582447 | ||||||
| chr4:83582474
|
C | T | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+642C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582474 | ||||||
| chr4:83582689
|
C | G | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+857C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582689 | ||||||
| chr4:83582756
|
C | T | 1 | a0001c0001t0004g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.479+924C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582756 | ||||||
| chr4:83582786
|
G | GT | 72 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.479+963dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83582786 | |||||
| chr4:83582786
|
G | T | 1 | a0001c0001t0003g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.479+954G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582786 | ||||||
| chr4:83582861
|
A | G | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.479+1029A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582861 | ||||||
| chr4:83583072
|
C | T | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+1240C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583072 | ||||||
| chr4:83583186
|
C | T | 6 | a0001c0001t0005g0005a0001c0001t0005g0206a0001c0001t0005g0219others(3): Show | 6 | HG00099.hp1 HG03130.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.479+1354C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583186 | ||||||
| chr4:83583293
|
C | CA | 9 | a0001c0001t0002g0300a0001c0001t0002g0311a0001c0001t0002g0323others(6): Show | 9 | HG00099.hp1 HG03130.hp1 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.479+1471dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583293 | |||||
| chr4:83583295
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.479+1463A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583295 | ||||||
| chr4:83583333
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.479+1501C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583333 | ||||||
| chr4:83583482
|
A | G | 13 | a0001c0001t0005g0179a0001c0001t0005g0191a0001c0001t0005g0195others(10): Show | 13 | HG02055.hp1 HG02809.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.479+1650A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583482 | ||||||
| chr4:83583517
|
A | G | 4 | a0001c0001t0006g0208a0001c0001t0007g0009a0001c0001t0007g0204others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+1685A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583517 | ||||||
| chr4:83583624
|
G | A | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.479+1792G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583624 | ||||||
| chr4:83583638
|
G | A | 3 | a0001c0001t0004g0187a0001c0001t0004g0307a0001c0001t0005g0247 | 3 | HG01243.hp1 HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.479+1806G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583638 | ||||||
| chr4:83583644
|
G | T | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+1812G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583644 | ||||||
| chr4:83583656
|
G | A | 11 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+1824G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583656 | ||||||
| chr4:83583658
|
C | G | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.479+1826C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583658 | ||||||
| chr4:83583666
|
T | TGAA | 16 | a0001c0001t0001g0153a0001c0001t0003g0011a0001c0001t0003g0013others(13): Show | 16 | HG00597.hp1 HG00609.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.479+1835_479+1837d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583666 | |||||
| chr4:83583667
|
G | GA | 121 | a0001c0001t0001g0075a0001c0001t0001g0084a0001c0001t0001g0086others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.479+1865dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | |||||
| chr4:83583667
|
G | GAA | 35 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(32): Show | 35 | HG00642.hp2 HG01109.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.479+1864_479+1865d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | |||||
| chr4:83583667
|
G | GAAAAAAA others(3): Show |
2 | a0001c0001t0007g0204a0001c0001t0007g0205 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.479+1856_479+1865d others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | |||||
| chr4:83583667
|
G | GAAAAAAA others(4): Show |
4 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0006g0001others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+1855_479+1865d others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | |||||
| chr4:83583667
|
G | GAAAAAAA others(5): Show |
1 | a0001c0001t0004g0215 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.479+1854_479+1865d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | |||||
| chr4:83583667
|
G | GAAAAAAA others(6): Show |
1 | a0001c0001t0006g0002 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.479+1853_479+1865d others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | |||||
| chr4:83583668
|
A | AAG | 54 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0059others(51): Show | 54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.479+1837_479+1838i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583668 | |||||
| chr4:83583704
|
T | G | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.479+1872T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583704 | ||||||
| chr4:83583826
|
T | G | 11 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+1994T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583826 | ||||||
| chr4:83583955
|
G | A | 2 | a0001c0001t0004g0041a0001c0001t0004g0043 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.479+2123G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583955 | ||||||
| chr4:83584170
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.479+2338C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584170 | ||||||
| chr4:83584378
|
C | T | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+2546C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584378 | ||||||
| chr4:83584457
|
G | A | 4 | a0001c0001t0002g0300a0001c0001t0002g0311a0001c0001t0002g0314others(1): Show | 4 | NA18947.hp2 NA18975.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+2625G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584457 | ||||||
| chr4:83584488
|
A | C | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+2656A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584488 | ||||||
| chr4:83584497
|
A | C | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+2665A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584497 | ||||||
| chr4:83584564
|
G | C | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-2691G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584564 | ||||||
| chr4:83584564
|
G | T | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.480-2691G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584564 | ||||||
| chr4:83584565
|
A | G | 87 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.480-2690A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584565 | ||||||
| chr4:83584609
|
G | T | 1 | a0001c0001t0002g0112 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.480-2646G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584609 | ||||||
| chr4:83584698
|
G | T | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-2557G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584698 | ||||||
| chr4:83584718
|
C | T | 1 | a0001c0001t0003g0239 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.480-2537C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584718 | ||||||
| chr4:83584863
|
T | C | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-2392T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584863 | ||||||
| chr4:83584920
|
C | G | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-2335C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584920 | ||||||
| chr4:83585039
|
T | C | 124 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0240others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.480-2216T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585039 | ||||||
| chr4:83585095
|
G | A | 7 | a0001c0001t0003g0023a0001c0001t0003g0024a0001c0001t0003g0027others(4): Show | 7 | HG01109.hp2 HG01175.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.480-2160G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585095 | ||||||
| chr4:83585127
|
A | C | 73 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.480-2128A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585127 | ||||||
| chr4:83585197
|
A | G | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-2058A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585197 | ||||||
| chr4:83585210
|
A | G | 1 | a0001c0001t0005g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.480-2045A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585210 | ||||||
| chr4:83585294
|
T | C | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1961T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585294 | ||||||
| chr4:83585331
|
A | C | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1924A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585331 | ||||||
| chr4:83585340
|
G | A | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1915G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585340 | ||||||
| chr4:83585383
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.480-1872A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585383 | ||||||
| chr4:83585513
|
A | C | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1742A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585513 | ||||||
| chr4:83585594
|
T | C | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1661T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585594 | ||||||
| chr4:83585615
|
CT | C | 75 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.480-1627delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83585615 | |||||
| chr4:83585716
|
G | A | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.480-1539G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585716 | ||||||
| chr4:83585833
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0206a0001c0001t0005g0219 | 3 | HG00099.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.480-1422C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585833 | ||||||
| chr4:83585851
|
T | G | 1 | a0001c0001t0013g0140 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.480-1404T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585851 | ||||||
| chr4:83585852
|
G | A | 1 | a0001c0001t0004g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.480-1403G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585852 | ||||||
| chr4:83585876
|
T | C | 1 | a0001c0001t0004g0310 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1379T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585876 | ||||||
| chr4:83585975
|
G | GCCAGACT | 14 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0003g0193others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.480-1278_480-1277i others(9): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83585975 | |||||
| chr4:83586119
|
A | C | 86 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.480-1136A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586119 | ||||||
| chr4:83586137
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.480-1118G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586137 | ||||||
| chr4:83586154
|
G | A | 1 | a0001c0001t0012g0245 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.480-1101G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586154 | ||||||
| chr4:83586183
|
C | G | 11 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0215others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.480-1072C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586183 | ||||||
| chr4:83586399
|
A | G | 14 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0003g0193others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.480-856A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586399 | ||||||
| chr4:83586409
|
T | C | 1 | a0001c0001t0005g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.480-846T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586409 | ||||||
| chr4:83586589
|
A | T | 219 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.480-666A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586589 | ||||||
| chr4:83586890
|
C | T | 2 | a0001c0001t0003g0068a0001c0001t0003g0151 | 2 | HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.480-365C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586890 | ||||||
| chr4:83587018
|
G | A | 6 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0206others(3): Show | 6 | HG00099.hp1 HG03130.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.480-237G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83587018 | ||||||
| chr4:83587543
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.554+214C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 4/11 | chr4 | 83587543 | ||||||
| chr4:83587611
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.554+282A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 4/11 | chr4 | 83587611 | ||||||
| chr4:83587676
|
T | G | 21 | a0001c0001t0003g0196a0001c0001t0004g0215a0001c0001t0005g0036others(18): Show | 21 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.554+347T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 4/11 | chr4 | 83587676 | ||||||
| chr4:83588032
|
A | G | 2 | a0001c0001t0005g0319a0001c0001t0014g0004 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.555-178A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 4/11 | chr4 | 83588032 | ||||||
| chr4:83588073
|
A | T | 8 | a0001c0001t0004g0215a0001c0001t0006g0001a0001c0001t0006g0002others(5): Show | 8 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-137A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 4/11 | chr4 | 83588073 | ||||||
| chr4:83588312
|
T | TG | 333 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0045others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.644+13_644+14insG | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588312 | ||||||
| chr4:83588444
|
G | A | 9 | a0001c0001t0002g0155a0001c0001t0002g0260a0001c0001t0002g0261others(6): Show | 9 | NA18943.hp2 NA18948.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.644+145G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588444 | ||||||
| chr4:83588502
|
C | T | 2 | a0001c0001t0001g0298a0001c0001t0001g0301 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.644+203C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588502 | ||||||
| chr4:83588584
|
A | C | 8 | a0001c0001t0003g0014a0001c0001t0003g0193a0001c0001t0005g0005others(5): Show | 8 | HG00099.hp1 HG02258.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.644+285A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588584 | ||||||
| chr4:83588698
|
C | G | 8 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0213others(5): Show | 8 | HG01884.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.644+399C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588698 | ||||||
| chr4:83588744
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.644+445T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588744 | ||||||
| chr4:83588855
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.644+556C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588855 | ||||||
| chr4:83589085
|
G | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG01081.hp1 HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.644+786G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83589085 | ||||||
| chr4:83589297
|
A | G | 2 | a0001c0001t0005g0197a0001c0001t0005g0247 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.645-902A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83589297 | ||||||
| chr4:83590055
|
T | C | 1 | a0001c0001t0003g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.645-144T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83590055 | ||||||
| chr4:83590401
|
C | T | 6 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | NA18946.hp2 NA18947.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+109C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83590401 | ||||||
| chr4:83590429
|
T | C | 11 | a0001c0001t0003g0014a0001c0001t0003g0193a0001c0001t0005g0005others(8): Show | 11 | HG00099.hp1 HG02258.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.738+137T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83590429 | ||||||
| chr4:83590457
|
G | A | 8 | a0001c0001t0003g0023a0001c0001t0003g0024a0001c0001t0003g0027others(5): Show | 8 | HG01109.hp2 HG01175.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.738+165G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83590457 | ||||||
| chr4:83590571
|
T | C | 174 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(171): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.738+279T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83590571 | ||||||
| chr4:83590856
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.738+564T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83590856 | ||||||
| chr4:83590885
|
C | CT | 77 | a0001c0001t0001g0096a0001c0001t0001g0160a0001c0001t0002g0183others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.738+613dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83590885 | |||||
| chr4:83590885
|
CT | C | 28 | a0001c0001t0001g0087a0001c0001t0001g0108a0001c0001t0001g0134others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.738+613delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83590885 | |||||
| chr4:83591060
|
G | A | 3 | a0001c0001t0003g0014a0001c0001t0003g0193a0001c0001t0005g0331 | 3 | HG02258.hp1 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.738+768G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591060 | ||||||
| chr4:83591142
|
G | A | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.738+850G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591142 | ||||||
| chr4:83591236
|
G | A | 174 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(171): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.738+944G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591236 | ||||||
| chr4:83591275
|
A | G | 1 | a0001c0004t0004g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.738+983A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591275 | ||||||
| chr4:83591299
|
A | T | 2 | a0001c0001t0005g0197a0001c0001t0005g0247 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.738+1007A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591299 | ||||||
| chr4:83591300
|
G | T | 2 | a0001c0001t0005g0197a0001c0001t0005g0247 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.738+1008G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591300 | ||||||
| chr4:83591301
|
G | T | 2 | a0001c0001t0005g0197a0001c0001t0005g0247 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.738+1009G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591301 | ||||||
| chr4:83591302
|
C | T | 2 | a0001c0001t0005g0197a0001c0001t0005g0247 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.738+1010C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591302 | ||||||
| chr4:83591330
|
T | C | 1 | a0001c0001t0003g0304 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.738+1038T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591330 | ||||||
| chr4:83591740
|
G | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0060 | 2 | HG03834.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.738+1448G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591740 | ||||||
| chr4:83591802
|
T | C | 1 | a0001c0001t0004g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.738+1510T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591802 | ||||||
| chr4:83592153
|
C | A | 1 | a0001c0001t0005g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.738+1861C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592153 | ||||||
| chr4:83592230
|
A | G | 8 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0122others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.738+1938A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592230 | ||||||
| chr4:83592236
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.738+1944G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592236 | ||||||
| chr4:83592285
|
C | G | 1 | a0001c0001t0005g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.738+1993C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592285 | ||||||
| chr4:83592394
|
T | C | 2 | a0001c0001t0004g0188a0001c0001t0004g0228 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.738+2102T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592394 | ||||||
| chr4:83592497
|
A | G | 73 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.738+2205A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592497 | ||||||
| chr4:83592825
|
A | G | 1 | a0001c0001t0003g0052 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.739-2020A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592825 | ||||||
| chr4:83592952
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.739-1893C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592952 | ||||||
| chr4:83593045
|
T | G | 1 | a0001c0001t0002g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.739-1800T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593045 | ||||||
| chr4:83593166
|
C | CTTTTTTT others(5): Show |
40 | a0001c0001t0003g0010a0001c0001t0003g0012a0001c0001t0003g0017others(37): Show | 40 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.739-1673_739-1662d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83593166 | |||||
| chr4:83593166
|
C | CTTTTTTT others(6): Show |
29 | a0001c0001t0003g0011a0001c0001t0003g0016a0001c0001t0003g0018others(26): Show | 29 | HG00597.hp1 HG00733.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.739-1674_739-1662d others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83593166 | |||||
| chr4:83593166
|
C | CTTTTTTT others(7): Show |
6 | a0001c0001t0003g0013a0001c0001t0003g0021a0001c0001t0003g0026others(3): Show | 6 | HG02056.hp1 HG02738.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.739-1675_739-1662d others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83593166 | |||||
| chr4:83593226
|
A | G | 333 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0045others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.739-1619A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593226 | ||||||
| chr4:83593307
|
G | A | 1 | a0001c0001t0003g0040 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.739-1538G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593307 | ||||||
| chr4:83593380
|
G | T | 1 | a0001c0001t0004g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.739-1465G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593380 | ||||||
| chr4:83593429
|
G | A | 4 | a0001c0001t0006g0208a0001c0001t0007g0009a0001c0001t0007g0204others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-1416G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593429 | ||||||
| chr4:83593449
|
AACC | A | 11 | a0001c0001t0005g0179a0001c0001t0005g0191a0001c0001t0005g0195others(8): Show | 11 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.739-1390_739-1388d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83593449 | |||||
| chr4:83593740
|
T | C | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.739-1105T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593740 | ||||||
| chr4:83593821
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0206a0001c0001t0005g0219 | 3 | HG00099.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.739-1024A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593821 | ||||||
| chr4:83593931
|
G | A | 2 | a0001c0001t0009g0007a0001c0001t0009g0008 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.739-914G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593931 | ||||||
| chr4:83593977
|
A | G | 1 | a0001c0001t0003g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.739-868A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593977 | ||||||
| chr4:83594246
|
T | C | 6 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.739-599T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594246 | ||||||
| chr4:83594254
|
C | T | 3 | a0001c0001t0005g0006a0001c0001t0005g0197a0001c0001t0005g0247 | 3 | HG02818.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.739-591C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594254 | ||||||
| chr4:83594428
|
T | G | 2 | a0001c0001t0005g0197a0001c0001t0005g0247 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.739-417T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594428 | ||||||
| chr4:83594503
|
T | C | 5 | a0001c0001t0002g0183a0001c0001t0002g0189a0001c0001t0002g0190others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.739-342T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594503 | ||||||
| chr4:83594622
|
G | A | 102 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.739-223G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594622 | ||||||
| chr4:83594640
|
C | T | 2 | a0001c0001t0003g0014a0001c0001t0005g0331 | 2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.739-205C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594640 | ||||||
| chr4:83594815
|
C | T | 73 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.739-30C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594815 | ||||||
| chr4:83595012
|
A | G | 11 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0118others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.854+52A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595012 | ||||||
| chr4:83595038
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0141 | 2 | NA18947.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.854+78C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595038 | ||||||
| chr4:83595323
|
A | AT | 11 | a0001c0001t0005g0179a0001c0001t0005g0191a0001c0001t0005g0195others(8): Show | 11 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.854+363_854+364ins others(1): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595323 | ||||||
| chr4:83595346
|
C | A | 6 | a0001c0001t0001g0102a0001c0001t0001g0134a0001c0001t0001g0136others(3): Show | 6 | HG02027.hp1 HG02040.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.854+386C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595346 | ||||||
| chr4:83595346
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.854+386C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595346 | ||||||
| chr4:83595536
|
G | A | 178 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.854+576G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595536 | ||||||
| chr4:83595603
|
G | A | 2 | a0001c0001t0004g0188a0001c0001t0004g0228 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.854+643G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595603 | ||||||
| chr4:83595607
|
C | G | 1 | a0001c0001t0003g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.854+647C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595607 | ||||||
| chr4:83595611
|
T | C | 7 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0207others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.854+651T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595611 | ||||||
| chr4:83595629
|
G | A | 9 | a0001c0001t0003g0196a0001c0001t0005g0036a0001c0001t0006g0001others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.854+669G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595629 | ||||||
| chr4:83595713
|
TA | T | 10 | a0001c0001t0001g0087a0001c0001t0001g0097a0001c0001t0001g0108others(7): Show | 10 | HG01169.hp1 HG01169.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.854+765delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 83595713 | |||||
| chr4:83595762
|
A | G | 4 | a0001c0001t0002g0300a0001c0001t0002g0311a0001c0001t0002g0314others(1): Show | 4 | NA18947.hp2 NA18975.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.854+802A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595762 | ||||||
| chr4:83595937
|
C | T | 3 | a0001c0001t0003g0297a0001c0001t0003g0304a0001c0001t0003g0328 | 3 | HG01169.hp2 HG02698.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.855-921C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595937 | ||||||
| chr4:83596233
|
C | G | 72 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.855-625C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596233 | ||||||
| chr4:83596391
|
C | T | 12 | a0001c0001t0005g0036a0001c0001t0005g0179a0001c0001t0005g0191others(9): Show | 12 | HG02723.hp2 HG02809.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.855-467C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596391 | ||||||
| chr4:83596437
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.855-421A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596437 | ||||||
| chr4:83596628
|
A | C | 1 | a0001c0001t0002g0250 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.855-230A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596628 | ||||||
| chr4:83596629
|
C | A | 1 | a0001c0001t0002g0250 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.855-229C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596629 | ||||||
| chr4:83596631
|
A | C | 1 | a0001c0001t0002g0250 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.855-227A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596631 | ||||||
| chr4:83596851
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA19062.hp2 | splice_region_variant&intron_variant | LOW | c.855-7T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596851 | ||||||
| chr4:83596854
|
A | G | 1 | a0001c0001t0002g0270 | 1 | NA18969.hp1 | splice_region_variant&intron_variant | LOW | c.855-4A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596854 | ||||||
| chr4:83597162
|
G | T | 178 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.910+249G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 8/11 | chr4 | 83597162 | ||||||
| chr4:83597184
|
C | T | 1 | a0001c0001t0003g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.911-246C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 8/11 | chr4 | 83597184 | ||||||
| chr4:83597211
|
A | G | 5 | a0001c0001t0005g0036a0001c0001t0006g0001a0001c0001t0006g0002others(2): Show | 5 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.911-219A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 8/11 | chr4 | 83597211 | ||||||
| chr4:83597341
|
A | G | 2 | a0001c0001t0004g0188a0001c0001t0004g0228 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.911-89A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 8/11 | chr4 | 83597341 | ||||||
| chr4:83597405
|
C | T | 73 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.911-25C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 8/11 | chr4 | 83597405 | ||||||
| chr4:83597678
|
C | T | 1 | a0001c0001t0003g0021 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.996+163C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597678 | ||||||
| chr4:83597688
|
A | G | 1 | a0001c0001t0006g0207 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.996+173A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597688 | ||||||
| chr4:83597739
|
A | G | 11 | a0001c0001t0003g0014a0001c0001t0003g0196a0001c0001t0005g0005others(8): Show | 11 | HG00099.hp1 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.996+224A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597739 | ||||||
| chr4:83597755
|
CAG | C | 5 | a0001c0001t0003g0016a0001c0001t0003g0019a0001c0001t0003g0033others(2): Show | 5 | HG00597.hp1 HG02015.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.996+242_996+243del others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 83597755 | |||||
| chr4:83597923
|
A | G | 189 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.997-128A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597923 | ||||||
| chr4:83597997
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.997-54C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597997 | ||||||
| chr4:83597998
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.997-53G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597998 | ||||||
| chr4:83598277
|
T | C | 1 | a0001c0001t0005g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1125+98T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | chr4 | 83598277 | ||||||
| chr4:83598430
|
C | T | 1 | a0001c0001t0002g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1126-214C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | chr4 | 83598430 | ||||||
| chr4:83598486
|
T | G | 215 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1126-158T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | chr4 | 83598486 | ||||||
| chr4:83598622
|
A | AT | 19 | a0001c0001t0002g0253a0001c0001t0002g0258a0001c0001t0002g0269others(16): Show | 19 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.1126-8dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 83598622 | |||||
| chr4:83598622
|
AT | A | 73 | a0001c0001t0001g0133a0001c0001t0001g0147a0001c0001t0001g0174others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
splice_region_variant&intron_variant | LOW | c.1126-8delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 83598622 | |||||
| chr4:83598625
|
T | G | 16 | a0001c0001t0005g0036a0001c0001t0005g0179a0001c0001t0005g0191others(13): Show | 16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1126-19T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | chr4 | 83598625 | ||||||
| chr4:83598751
|
C | CT | 12 | a0001c0001t0001g0070a0001c0001t0001g0085a0001c0001t0001g0107others(9): Show | 12 | HG01433.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1205+64dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
C | CTT | 7 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0004g0041others(4): Show | 7 | HG00099.hp1 HG01496.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.1205+63_1205+64dup others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
C | CTTT | 8 | a0001c0001t0002g0213a0001c0001t0002g0265a0001c0001t0002g0277others(5): Show | 8 | HG02040.hp1 HG02897.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1205+62_1205+64dup others(3): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
C | CTTTT | 50 | a0001c0001t0001g0226a0001c0001t0002g0025a0001c0001t0002g0039others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1205+61_1205+64dup others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
C | CTTTTT | 44 | a0001c0001t0001g0225a0001c0001t0002g0015a0001c0001t0002g0079others(41): Show | 44 | HG00140.hp1 HG00438.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1205+60_1205+64dup others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
C | CTTTTTT | 8 | a0001c0001t0002g0186a0001c0001t0002g0278a0001c0001t0002g0300others(5): Show | 8 | HG00733.hp1 HG02004.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.1205+59_1205+64dup others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
CT | C | 58 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(55): Show | 58 | HG00438.hp1 HG00597.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.1205+64delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
CTTTT | C | 17 | a0001c0001t0003g0011a0001c0001t0003g0019a0001c0001t0003g0030others(14): Show | 17 | HG00140.hp2 HG00639.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1205+61_1205+64del others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
CTTTTT | C | 52 | a0001c0001t0003g0010a0001c0001t0003g0012a0001c0001t0003g0013others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1205+60_1205+64del others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
CTTTTTT | C | 7 | a0001c0001t0002g0330a0001c0001t0003g0023a0001c0001t0003g0027others(4): Show | 7 | HG01175.hp1 HG02004.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1205+59_1205+64del others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1205+55_1205+64del others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1205+54_1205+64del others(11): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0308 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1205+52_1205+64del others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0069 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1205+51_1205+64del others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0002g0274 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1205+46_1205+64del others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598751
|
CTTTTTTT others(17): Show |
C | 7 | a0001c0001t0005g0191a0001c0001t0005g0195a0001c0001t0005g0220others(4): Show | 7 | HG02896.hp1 HG02897.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1205+41_1205+64del others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | |||||
| chr4:83598830
|
ATGATCAT others(14): Show |
A | 2 | a0001c0001t0001g0102a0001c0001t0001g0136 | 2 | HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1205+130_1205+150d others(23): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598830 | |||||
| chr4:83598877
|
C | T | 72 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1205+154C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83598877 | ||||||
| chr4:83598888
|
C | G | 11 | a0001c0001t0005g0179a0001c0001t0005g0191a0001c0001t0005g0195others(8): Show | 11 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1205+165C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83598888 | ||||||
| chr4:83599082
|
C | A | 84 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1205+359C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599082 | ||||||
| chr4:83599524
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1205+801T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599524 | ||||||
| chr4:83599534
|
T | G | 189 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1205+811T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599534 | ||||||
| chr4:83599545
|
C | G | 189 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1205+822C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599545 | ||||||
| chr4:83599864
|
T | G | 1 | a0001c0001t0002g0259 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1205+1141T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599864 | ||||||
| chr4:83599865
|
G | T | 1 | a0001c0001t0002g0259 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1205+1142G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599865 | ||||||
| chr4:83599948
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | NA18939.hp2 NA19011.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1205+1225A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599948 | ||||||
| chr4:83599963
|
T | C | 11 | a0001c0001t0003g0014a0001c0001t0003g0196a0001c0001t0005g0005others(8): Show | 11 | HG00099.hp1 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1205+1240T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599963 | ||||||
| chr4:83600124
|
A | C | 200 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1205+1401A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600124 | ||||||
| chr4:83600131
|
T | C | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1205+1408T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600131 | ||||||
| chr4:83600328
|
C | CCAT | 178 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1205+1606_1205+160 others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83600328 | |||||
| chr4:83600330
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1205+1607A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600330 | ||||||
| chr4:83600385
|
A | G | 7 | a0001c0001t0003g0014a0001c0001t0005g0005a0001c0001t0005g0206others(4): Show | 7 | HG00099.hp1 HG02258.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1205+1662A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600385 | ||||||
| chr4:83600479
|
T | C | 73 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1205+1756T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600479 | ||||||
| chr4:83600503
|
A | AATT | 178 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1205+1796_1205+179 others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83600503 | |||||
| chr4:83600531
|
G | A | 1 | a0001c0001t0005g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1205+1808G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600531 | ||||||
| chr4:83600621
|
G | C | 3 | a0001c0001t0003g0071a0001c0001t0003g0144a0001c0001t0003g0212 | 3 | HG00280.hp2 HG01081.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1205+1898G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600621 | ||||||
| chr4:83600664
|
A | G | 179 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1205+1941A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600664 | ||||||
| chr4:83600669
|
A | AT | 12 | a0001c0001t0003g0023a0001c0001t0003g0024a0001c0001t0003g0027others(9): Show | 12 | HG01109.hp2 HG01175.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.1205+1954dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83600669 | |||||
| chr4:83600694
|
T | C | 205 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0015others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1205+1971T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600694 | ||||||
| chr4:83600827
|
C | T | 1 | a0003c0003t0002g0284 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1205+2104C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600827 | ||||||
| chr4:83600927
|
T | G | 6 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1205+2204T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600927 | ||||||
| chr4:83601021
|
C | T | 3 | a0001c0001t0002g0227a0001c0001t0002g0312a0001c0001t0002g0313 | 3 | HG01884.hp1 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1205+2298C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601021 | ||||||
| chr4:83601438
|
G | T | 1 | a0001c0001t0002g0329 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1205+2715G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601438 | ||||||
| chr4:83601564
|
G | A | 17 | a0001c0001t0005g0006a0001c0001t0005g0036a0001c0001t0005g0179others(14): Show | 17 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.1205+2841G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601564 | ||||||
| chr4:83601624
|
G | A | 4 | a0001c0001t0006g0001a0001c0001t0006g0002a0001c0001t0006g0207others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1205+2901G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601624 | ||||||
| chr4:83601631
|
T | C | 2 | a0001c0001t0004g0188a0001c0001t0004g0228 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1205+2908T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601631 | ||||||
| chr4:83601647
|
C | T | 1 | a0001c0001t0002g0269 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1205+2924C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601647 | ||||||
| chr4:83601731
|
G | C | 1 | a0001c0001t0003g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1206-2937G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601731 | ||||||
| chr4:83601740
|
C | T | 103 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0039others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1206-2928C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601740 | ||||||
| chr4:83601876
|
T | C | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1206-2792T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601876 | ||||||
| chr4:83601949
|
T | C | 207 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0039others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1206-2719T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601949 | ||||||
| chr4:83601950
|
C | G | 1 | a0001c0001t0002g0259 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1206-2718C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601950 | ||||||
| chr4:83602019
|
T | C | 1 | a0001c0001t0006g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1206-2649T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602019 | ||||||
| chr4:83602075
|
A | T | 1 | a0003c0003t0002g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1206-2593A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602075 | ||||||
| chr4:83602118
|
A | G | 8 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(5): Show | 8 | HG02258.hp2 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1206-2550A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602118 | ||||||
| chr4:83602122
|
G | T | 1 | a0001c0001t0003g0047 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1206-2546G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602122 | ||||||
| chr4:83602162
|
T | A | 1 | a0001c0001t0005g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1206-2506T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602162 | ||||||
| chr4:83602467
|
T | G | 1 | a0001c0001t0003g0047 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1206-2201T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602467 | ||||||
| chr4:83602557
|
AAG | A | 74 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1206-2109_1206-210 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83602557 | |||||
| chr4:83602588
|
G | C | 1 | a0001c0001t0005g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1206-2080G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602588 | ||||||
| chr4:83602613
|
TA | T | 188 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0039others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1206-2053delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83602613 | |||||
| chr4:83602766
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1206-1902C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602766 | ||||||
| chr4:83603037
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1206-1631G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603037 | ||||||
| chr4:83603330
|
C | A | 72 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1206-1338C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603330 | ||||||
| chr4:83603439
|
A | G | 207 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0039others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1206-1229A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603439 | ||||||
| chr4:83603470
|
C | T | 177 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0039others(174): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1206-1198C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603470 | ||||||
| chr4:83603589
|
G | A | 1 | a0001c0001t0003g0050 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1206-1079G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603589 | ||||||
| chr4:83603647
|
G | A | 2 | a0001c0001t0002g0259a0001c0001t0002g0264 | 2 | HG00408.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1206-1021G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603647 | ||||||
| chr4:83603739
|
AAGATTGT others(28): Show |
A | 1 | a0001c0001t0002g0265 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1206-926_1206-892d others(37): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83603739 | |||||
| chr4:83603790
|
C | CA | 12 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0102others(9): Show | 12 | HG01261.hp1 HG02027.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1206-856dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83603790 | |||||
| chr4:83603790
|
CA | C | 19 | a0001c0001t0001g0101a0001c0001t0001g0126a0001c0001t0001g0137others(16): Show | 19 | HG01346.hp1 HG01993.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1206-856delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83603790 | |||||
| chr4:83603790
|
CAAA | C | 175 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0039others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1206-858_1206-856d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83603790 | |||||
| chr4:83603790
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0037a0001c0001t0001g0045a0001c0001t0001g0150 | 3 | HG00741.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1206-865_1206-856d others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83603790 | |||||
| chr4:83603804
|
A | C | 177 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0039others(174): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1206-864A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603804 | ||||||
| chr4:83603907
|
A | G | 13 | a0001c0001t0005g0179a0001c0001t0005g0191a0001c0001t0005g0195others(10): Show | 13 | HG02809.hp1 HG02818.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.1206-761A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603907 | ||||||
| chr4:83603986
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-682A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603986 | ||||||
| chr4:83603991
|
A | T | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-677A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603991 | ||||||
| chr4:83603999
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-669G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603999 | ||||||
| chr4:83604000
|
T | A | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-668T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604000 | ||||||
| chr4:83604021
|
G | T | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-647G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604021 | ||||||
| chr4:83604023
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-645G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604023 | ||||||
| chr4:83604045
|
T | A | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-623T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604045 | ||||||
| chr4:83604048
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-620T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604048 | ||||||
| chr4:83604050
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-618G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604050 | ||||||
| chr4:83604055
|
A | T | 74 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1206-613A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604055 | ||||||
| chr4:83604063
|
T | TTTTG | 3 | a0001c0001t0004g0041a0001c0001t0004g0042a0001c0001t0004g0043 | 3 | HG02145.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1206-585_1206-582d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83604063 | |||||
| chr4:83604065
|
T | A | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-603T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604065 | ||||||
| chr4:83604067
|
G | T | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-601G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604067 | ||||||
| chr4:83604070
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-598T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604070 | ||||||
| chr4:83604071
|
G | T | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-597G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604071 | ||||||
| chr4:83604075
|
G | T | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-593G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604075 | ||||||
| chr4:83604083
|
G | T | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-585G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604083 | ||||||
| chr4:83604093
|
C | T | 103 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0039others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1206-575C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604093 | ||||||
| chr4:83604094
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-574G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604094 | ||||||
| chr4:83604095
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-573A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604095 | ||||||
| chr4:83604112
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-556C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604112 | ||||||
| chr4:83604128
|
A | G | 73 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0012others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1206-540A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604128 | ||||||
| chr4:83604134
|
T | A | 1 | a0001c0001t0003g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-534T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604134 | ||||||
| chr4:83604141
|
G | T | 1 | a0001c0001t0002g0238 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1206-527G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604141 | ||||||
| chr4:83604142
|
G | C | 1 | a0001c0001t0002g0238 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1206-526G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604142 | ||||||
| chr4:83604163
|
C | T | 1 | a0001c0001t0004g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1206-505C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604163 | ||||||
| chr4:83604220
|
C | T | 1 | a0001c0001t0005g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1206-448C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604220 | ||||||
| chr4:83604228
|
T | G | 103 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0039others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1206-440T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604228 | ||||||
| chr4:83604270
|
T | C | 207 | a0001c0001t0002g0015a0001c0001t0002g0025a0001c0001t0002g0039others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1206-398T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604270 | ||||||
| chr4:83604554
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0101a0001c0001t0001g0137 | 3 | HG01346.hp1 HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1206-114A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604554 |