Search by Gene
| geneid | 56894 |
|---|---|
| ensemblid | ENSG00000160216.21 |
| hgncid | 326 |
| symbol | AGPAT3 |
| name | 1-acylglycerol-3-phosphate O-acyltransferase 3 |
| refseq_nuc | NM_020132.5 |
| refseq_prot | NP_064517.1 |
| ensembl_nuc | ENST00000291572.13 |
| ensembl_prot | ENSP00000291572.8 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 43865223 |
| end | 43987592 |
| strand | + |
| ver | v1.2 |
| region | chr21:43865223-43987592 |
| region5000 | chr21:43860223-43992592 |
| regionname0 | AGPAT3_chr21_43865223_43987592 |
| regionname5000 | AGPAT3_chr21_43860223_43992592 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 376 | 340 | 89 | 70 | 124 | 15 | 40 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0002 | 0/0 | 376 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0003 | 0/0 | 376 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1131 | 332 | 85 | 70 | 124 | 15 | 36 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| c0002 | 0/0 | 1131 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| c0003 | 0/0 | 1131 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| c0004 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| c0005 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| c0006 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| c0007 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| c0008 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| c0009 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 5435 | 101 | 5 | 20 | 55 | 11 | 8 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0002 | 0/0 | 5437 | 37 | 7 | 2 | 22 | 0 | 6 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0003 | 0/0 | 5435 | 28 | 7 | 0 | 20 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0004 | 0/0 | 5436 | 26 | 0 | 16 | 8 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0005 | 0/0 | 5435 | 7 | 1 | 2 | 0 | 0 | 4 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0006 | 0/0 | 5435 | 7 | 6 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0007 | 0/0 | 5435 | 7 | 5 | 0 | 2 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0008 | 0/0 | 5435 | 6 | 0 | 0 | 0 | 2 | 4 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0009 | 0/0 | 5435 | 6 | 0 | 6 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0010 | 0/0 | 5435 | 5 | 2 | 1 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0011 | 0/0 | 5435 | 5 | 0 | 0 | 3 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0012 | 0/0 | 5434 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0013 | 0/0 | 5436 | 4 | 0 | 0 | 1 | 0 | 3 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0014 | 0/0 | 5435 | 4 | 0 | 2 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0015 | 0/0 | 5433 | 4 | 2 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0016 | 0/0 | 5436 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0017 | 0/0 | 5434 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0018 | 0/0 | 5434 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0019 | 0/0 | 5435 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0020 | 0/0 | 5434 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0021 | 0/0 | 5435 | 3 | 0 | 2 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0022 | 0/0 | 5436 | 3 | 0 | 2 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0023 | 0/0 | 5435 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0024 | 0/0 | 5435 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0025 | 0/0 | 5433 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0026 | 0/0 | 5437 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0027 | 0/0 | 5435 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0028 | 0/0 | 5435 | 2 | 0 | 1 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0029 | 0/0 | 5436 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0030 | 0/0 | 5435 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0031 | 0/0 | 5435 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0032 | 0/0 | 5435 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0033 | 0/0 | 5436 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0034 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0035 | 0/0 | 5435 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0036 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0037 | 0/0 | 5433 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0038 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0039 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0040 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0041 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0042 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0043 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0044 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0045 | 0/0 | 5436 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0046 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0047 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0048 | 0/0 | 5436 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0049 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0050 | 0/0 | 5436 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0051 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0052 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0053 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0054 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0055 | 0/0 | 5436 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0056 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0057 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0058 | 0/0 | 5435 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0059 | 0/0 | 5435 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0060 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0061 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0062 | 0/0 | 5436 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0063 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0064 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0065 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0066 | 0/0 | 5435 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0067 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0068 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0069 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0070 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0071 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0072 | 0/0 | 5433 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0073 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0074 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0075 | 0/0 | 5435 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0076 | 0/0 | 5436 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0077 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0078 | 0/0 | 5437 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0079 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0080 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| t0081 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 332 | 85 | 70 | 124 | 15 | 36 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0009 | a0001 | c0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0002c0006 | a0002 | c0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0003c0007 | a0003 | c0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 99 | 5 | 20 | 55 | 10 | 7 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 35 | 6 | 2 | 22 | 0 | 5 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 28 | 7 | 0 | 20 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 26 | 0 | 16 | 8 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 7 | 1 | 2 | 0 | 0 | 4 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 7 | 5 | 0 | 2 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 6 | 0 | 0 | 0 | 2 | 4 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0025 | a0001 | c0001 | t0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0026 | a0001 | c0001 | t0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0027 | a0001 | c0001 | t0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0028 | a0001 | c0001 | t0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0029 | a0001 | c0001 | t0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0030 | a0001 | c0001 | t0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0031 | a0001 | c0001 | t0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0032 | a0001 | c0001 | t0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0033 | a0001 | c0001 | t0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0036 | a0001 | c0001 | t0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0037 | a0001 | c0001 | t0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0038 | a0001 | c0001 | t0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0039 | a0001 | c0001 | t0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0040 | a0001 | c0001 | t0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0041 | a0001 | c0001 | t0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0042 | a0001 | c0001 | t0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0043 | a0001 | c0001 | t0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0044 | a0001 | c0001 | t0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0045 | a0001 | c0001 | t0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0046 | a0001 | c0001 | t0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0047 | a0001 | c0001 | t0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0049 | a0001 | c0001 | t0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0050 | a0001 | c0001 | t0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0051 | a0001 | c0001 | t0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0052 | a0001 | c0001 | t0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0053 | a0001 | c0001 | t0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0054 | a0001 | c0001 | t0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0055 | a0001 | c0001 | t0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0056 | a0001 | c0001 | t0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0057 | a0001 | c0001 | t0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0058 | a0001 | c0001 | t0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0059 | a0001 | c0001 | t0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0060 | a0001 | c0001 | t0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0061 | a0001 | c0001 | t0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0062 | a0001 | c0001 | t0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0063 | a0001 | c0001 | t0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0064 | a0001 | c0001 | t0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0065 | a0001 | c0001 | t0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0066 | a0001 | c0001 | t0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0067 | a0001 | c0001 | t0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0068 | a0001 | c0001 | t0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0069 | a0001 | c0001 | t0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0070 | a0001 | c0001 | t0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0072 | a0001 | c0001 | t0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0073 | a0001 | c0001 | t0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0074 | a0001 | c0001 | t0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0075 | a0001 | c0001 | t0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0076 | a0001 | c0001 | t0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0077 | a0001 | c0001 | t0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0078 | a0001 | c0001 | t0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0079 | a0001 | c0001 | t0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0080 | a0001 | c0001 | t0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0001t0081 | a0001 | c0001 | t0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0002t0018 | a0001 | c0002 | t0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0002t0048 | a0001 | c0002 | t0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0003t0011 | a0001 | c0003 | t0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0004t0002 | a0001 | c0004 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0008t0071 | a0001 | c0008 | t0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0001c0009t0002 | a0001 | c0009 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0002c0006t0010 | a0002 | c0006 | t0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| a0003c0007t0001 | a0003 | c0007 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0222 | a0001 | c0001 | t0001 | g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0225 | a0001 | c0001 | t0001 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0237 | a0001 | c0001 | t0001 | g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0243 | a0001 | c0001 | t0001 | g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0245 | a0001 | c0001 | t0001 | g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0247 | a0001 | c0001 | t0001 | g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0248 | a0001 | c0001 | t0001 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0252 | a0001 | c0001 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0253 | a0001 | c0001 | t0001 | g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0255 | a0001 | c0001 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0256 | a0001 | c0001 | t0001 | g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0263 | a0001 | c0001 | t0001 | g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0264 | a0001 | c0001 | t0001 | g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0265 | a0001 | c0001 | t0001 | g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0268 | a0001 | c0001 | t0001 | g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0270 | a0001 | c0001 | t0001 | g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0271 | a0001 | c0001 | t0001 | g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0274 | a0001 | c0001 | t0001 | g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0275 | a0001 | c0001 | t0001 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0276 | a0001 | c0001 | t0001 | g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0280 | a0001 | c0001 | t0001 | g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0282 | a0001 | c0001 | t0001 | g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0283 | a0001 | c0001 | t0001 | g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0285 | a0001 | c0001 | t0001 | g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0287 | a0001 | c0001 | t0001 | g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0289 | a0001 | c0001 | t0001 | g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0290 | a0001 | c0001 | t0001 | g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0291 | a0001 | c0001 | t0001 | g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0292 | a0001 | c0001 | t0001 | g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0294 | a0001 | c0001 | t0001 | g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0295 | a0001 | c0001 | t0001 | g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0297 | a0001 | c0001 | t0001 | g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0300 | a0001 | c0001 | t0001 | g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0305 | a0001 | c0001 | t0001 | g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0309 | a0001 | c0001 | t0001 | g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0310 | a0001 | c0001 | t0001 | g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0001g0334 | a0001 | c0001 | t0001 | g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0014 | a0001 | c0001 | t0002 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0016 | a0001 | c0001 | t0002 | g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0019 | a0001 | c0001 | t0002 | g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0023 | a0001 | c0001 | t0002 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0040 | a0001 | c0001 | t0002 | g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0041 | a0001 | c0001 | t0002 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0049 | a0001 | c0001 | t0002 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0050 | a0001 | c0001 | t0002 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0060 | a0001 | c0001 | t0002 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0078 | a0001 | c0001 | t0002 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0120 | a0001 | c0001 | t0002 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0132 | a0001 | c0001 | t0002 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0149 | a0001 | c0001 | t0002 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0171 | a0001 | c0001 | t0002 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0178 | a0001 | c0001 | t0002 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0183 | a0001 | c0001 | t0002 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0189 | a0001 | c0001 | t0002 | g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0199 | a0001 | c0001 | t0002 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0219 | a0001 | c0001 | t0002 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0224 | a0001 | c0001 | t0002 | g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0238 | a0001 | c0001 | t0002 | g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0246 | a0001 | c0001 | t0002 | g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0258 | a0001 | c0001 | t0002 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0267 | a0001 | c0001 | t0002 | g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0296 | a0001 | c0001 | t0002 | g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0307 | a0001 | c0001 | t0002 | g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0332 | a0001 | c0001 | t0002 | g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0333 | a0001 | c0001 | t0002 | g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0335 | a0001 | c0001 | t0002 | g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0336 | a0001 | c0001 | t0002 | g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0337 | a0001 | c0001 | t0002 | g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0338 | a0001 | c0001 | t0002 | g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0002g0339 | a0001 | c0001 | t0002 | g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0002 | a0001 | c0001 | t0003 | g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0080 | a0001 | c0001 | t0003 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0085 | a0001 | c0001 | t0003 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0119 | a0001 | c0001 | t0003 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0121 | a0001 | c0001 | t0003 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0123 | a0001 | c0001 | t0003 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0124 | a0001 | c0001 | t0003 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0125 | a0001 | c0001 | t0003 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0127 | a0001 | c0001 | t0003 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0128 | a0001 | c0001 | t0003 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0129 | a0001 | c0001 | t0003 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0130 | a0001 | c0001 | t0003 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0131 | a0001 | c0001 | t0003 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0135 | a0001 | c0001 | t0003 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0137 | a0001 | c0001 | t0003 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0139 | a0001 | c0001 | t0003 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0140 | a0001 | c0001 | t0003 | g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0153 | a0001 | c0001 | t0003 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0160 | a0001 | c0001 | t0003 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0161 | a0001 | c0001 | t0003 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0167 | a0001 | c0001 | t0003 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0181 | a0001 | c0001 | t0003 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0236 | a0001 | c0001 | t0003 | g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0288 | a0001 | c0001 | t0003 | g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0306 | a0001 | c0001 | t0003 | g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0308 | a0001 | c0001 | t0003 | g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0003g0319 | a0001 | c0001 | t0003 | g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0003 | a0001 | c0001 | t0004 | g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0004 | a0001 | c0001 | t0004 | g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0010 | a0001 | c0001 | t0004 | g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0011 | a0001 | c0001 | t0004 | g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0012 | a0001 | c0001 | t0004 | g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0029 | a0001 | c0001 | t0004 | g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0038 | a0001 | c0001 | t0004 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0044 | a0001 | c0001 | t0004 | g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0047 | a0001 | c0001 | t0004 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0079 | a0001 | c0001 | t0004 | g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0126 | a0001 | c0001 | t0004 | g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0185 | a0001 | c0001 | t0004 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0188 | a0001 | c0001 | t0004 | g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0190 | a0001 | c0001 | t0004 | g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0193 | a0001 | c0001 | t0004 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0203 | a0001 | c0001 | t0004 | g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0240 | a0001 | c0001 | t0004 | g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0244 | a0001 | c0001 | t0004 | g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0278 | a0001 | c0001 | t0004 | g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0281 | a0001 | c0001 | t0004 | g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0286 | a0001 | c0001 | t0004 | g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0311 | a0001 | c0001 | t0004 | g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0312 | a0001 | c0001 | t0004 | g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0314 | a0001 | c0001 | t0004 | g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0317 | a0001 | c0001 | t0004 | g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0004g0340 | a0001 | c0001 | t0004 | g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0005g0082 | a0001 | c0001 | t0005 | g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0005g0086 | a0001 | c0001 | t0005 | g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0005g0088 | a0001 | c0001 | t0005 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0005g0089 | a0001 | c0001 | t0005 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0005g0090 | a0001 | c0001 | t0005 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0005g0111 | a0001 | c0001 | t0005 | g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0005g0322 | a0001 | c0001 | t0005 | g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0006g0045 | a0001 | c0001 | t0006 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0006g0061 | a0001 | c0001 | t0006 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0006g0074 | a0001 | c0001 | t0006 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0006g0097 | a0001 | c0001 | t0006 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0006g0194 | a0001 | c0001 | t0006 | g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0006g0205 | a0001 | c0001 | t0006 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0006g0241 | a0001 | c0001 | t0006 | g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0007g0122 | a0001 | c0001 | t0007 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0007g0154 | a0001 | c0001 | t0007 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0007g0192 | a0001 | c0001 | t0007 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0007g0326 | a0001 | c0001 | t0007 | g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0007g0327 | a0001 | c0001 | t0007 | g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0007g0328 | a0001 | c0001 | t0007 | g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0007g0329 | a0001 | c0001 | t0007 | g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0008g0039 | a0001 | c0001 | t0008 | g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0008g0042 | a0001 | c0001 | t0008 | g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0008g0043 | a0001 | c0001 | t0008 | g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0008g0143 | a0001 | c0001 | t0008 | g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0008g0158 | a0001 | c0001 | t0008 | g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0008g0159 | a0001 | c0001 | t0008 | g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0009g0030 | a0001 | c0001 | t0009 | g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0009g0226 | a0001 | c0001 | t0009 | g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0009g0227 | a0001 | c0001 | t0009 | g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0009g0229 | a0001 | c0001 | t0009 | g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0009g0230 | a0001 | c0001 | t0009 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0009g0284 | a0001 | c0001 | t0009 | g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0010g0063 | a0001 | c0001 | t0010 | g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0010g0095 | a0001 | c0001 | t0010 | g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0010g0096 | a0001 | c0001 | t0010 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0010g0110 | a0001 | c0001 | t0010 | g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0011g0021 | a0001 | c0001 | t0011 | g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0011g0166 | a0001 | c0001 | t0011 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0011g0204 | a0001 | c0001 | t0011 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0012g0070 | a0001 | c0001 | t0012 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0012g0076 | a0001 | c0001 | t0012 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0012g0099 | a0001 | c0001 | t0012 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0012g0101 | a0001 | c0001 | t0012 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0013g0005 | a0001 | c0001 | t0013 | g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0013g0006 | a0001 | c0001 | t0013 | g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0013g0239 | a0001 | c0001 | t0013 | g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0013g0249 | a0001 | c0001 | t0013 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0014g0198 | a0001 | c0001 | t0014 | g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0014g0234 | a0001 | c0001 | t0014 | g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0014g0259 | a0001 | c0001 | t0014 | g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0014g0266 | a0001 | c0001 | t0014 | g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0015g0115 | a0001 | c0001 | t0015 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0015g0116 | a0001 | c0001 | t0015 | g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0015g0117 | a0001 | c0001 | t0015 | g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0015g0118 | a0001 | c0001 | t0015 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0016g0071 | a0001 | c0001 | t0016 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0016g0072 | a0001 | c0001 | t0016 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0016g0075 | a0001 | c0001 | t0016 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0017g0077 | a0001 | c0001 | t0017 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0017g0098 | a0001 | c0001 | t0017 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0017g0100 | a0001 | c0001 | t0017 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0018g0081 | a0001 | c0001 | t0018 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0018g0084 | a0001 | c0001 | t0018 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0019g0069 | a0001 | c0001 | t0019 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0019g0323 | a0001 | c0001 | t0019 | g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0019g0330 | a0001 | c0001 | t0019 | g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0020g0064 | a0001 | c0001 | t0020 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0020g0065 | a0001 | c0001 | t0020 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0020g0066 | a0001 | c0001 | t0020 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0021g0062 | a0001 | c0001 | t0021 | g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0021g0262 | a0001 | c0001 | t0021 | g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0021g0272 | a0001 | c0001 | t0021 | g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0022g0032 | a0001 | c0001 | t0022 | g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0022g0051 | a0001 | c0001 | t0022 | g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0022g0055 | a0001 | c0001 | t0022 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0023g0001 | a0001 | c0001 | t0023 | g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0024g0106 | a0001 | c0001 | t0024 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0024g0107 | a0001 | c0001 | t0024 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0025g0087 | a0001 | c0001 | t0025 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0025g0108 | a0001 | c0001 | t0025 | g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0026g0059 | a0001 | c0001 | t0026 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0026g0191 | a0001 | c0001 | t0026 | g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0027g0067 | a0001 | c0001 | t0027 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0027g0299 | a0001 | c0001 | t0027 | g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0028g0018 | a0001 | c0001 | t0028 | g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0028g0242 | a0001 | c0001 | t0028 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0029g0083 | a0001 | c0001 | t0029 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0029g0144 | a0001 | c0001 | t0029 | g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0030g0073 | a0001 | c0001 | t0030 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0030g0331 | a0001 | c0001 | t0030 | g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0031g0195 | a0001 | c0001 | t0031 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0031g0196 | a0001 | c0001 | t0031 | g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0032g0324 | a0001 | c0001 | t0032 | g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0032g0325 | a0001 | c0001 | t0032 | g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0033g0212 | a0001 | c0001 | t0033 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0033g0213 | a0001 | c0001 | t0033 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0034g0105 | a0001 | c0001 | t0034 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0035g0303 | a0001 | c0001 | t0035 | g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0036g0094 | a0001 | c0001 | t0036 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0037g0304 | a0001 | c0001 | t0037 | g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0038g0109 | a0001 | c0001 | t0038 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0039g0102 | a0001 | c0001 | t0039 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0040g0007 | a0001 | c0001 | t0040 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0041g0091 | a0001 | c0001 | t0041 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0042g0092 | a0001 | c0001 | t0042 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0043g0103 | a0001 | c0001 | t0043 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0044g0093 | a0001 | c0001 | t0044 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0045g0104 | a0001 | c0001 | t0045 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0046g0133 | a0001 | c0001 | t0046 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0047g0025 | a0001 | c0001 | t0047 | g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0049g0320 | a0001 | c0001 | t0049 | g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0050g0024 | a0001 | c0001 | t0050 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0051g0207 | a0001 | c0001 | t0051 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0052g0220 | a0001 | c0001 | t0052 | g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0053g0321 | a0001 | c0001 | t0053 | g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0054g0022 | a0001 | c0001 | t0054 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0055g0318 | a0001 | c0001 | t0055 | g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0056g0141 | a0001 | c0001 | t0056 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0057g0208 | a0001 | c0001 | t0057 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0058g0315 | a0001 | c0001 | t0058 | g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0059g0033 | a0001 | c0001 | t0059 | g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0060g0302 | a0001 | c0001 | t0060 | g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0061g0250 | a0001 | c0001 | t0061 | g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0062g0313 | a0001 | c0001 | t0062 | g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0063g0273 | a0001 | c0001 | t0063 | g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0064g0147 | a0001 | c0001 | t0064 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0065g0020 | a0001 | c0001 | t0065 | g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0066g0027 | a0001 | c0001 | t0066 | g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0067g0277 | a0001 | c0001 | t0067 | g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0068g0013 | a0001 | c0001 | t0068 | g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0069g0301 | a0001 | c0001 | t0069 | g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0070g0134 | a0001 | c0001 | t0070 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0072g0209 | a0001 | c0001 | t0072 | g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0073g0053 | a0001 | c0001 | t0073 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0074g0211 | a0001 | c0001 | t0074 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0075g0008 | a0001 | c0001 | t0075 | g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0076g0279 | a0001 | c0001 | t0076 | g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0077g0254 | a0001 | c0001 | t0077 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0078g0316 | a0001 | c0001 | t0078 | g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0079g0228 | a0001 | c0001 | t0079 | g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0080g0187 | a0001 | c0001 | t0080 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0001t0081g0136 | a0001 | c0001 | t0081 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0002t0018g0114 | a0001 | c0002 | t0018 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0002t0048g0298 | a0001 | c0002 | t0048 | g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0003t0011g0260 | a0001 | c0003 | t0011 | g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0003t0011g0261 | a0001 | c0003 | t0011 | g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0004t0002g0138 | a0001 | c0004 | t0002 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0005t0001g0293 | a0001 | c0005 | t0001 | g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0008t0071g0068 | a0001 | c0008 | t0071 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0001c0009t0002g0186 | a0001 | c0009 | t0002 | g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0002c0006t0010g0112 | a0002 | c0006 | t0010 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| a0003c0007t0001g0052 | a0003 | c0007 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0076 | g0279 | EUR | GBR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | FIN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00323 | hp1 | a0001 | c0001 | t0021 | g0062 | EUR | FIN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00323 | hp2 | a0001 | c0001 | t0008 | g0143 | EUR | FIN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00558 | hp2 | a0001 | c0001 | t0033 | g0213 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00639 | hp1 | a0001 | c0001 | t0010 | g0095 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0244 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0278 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0240 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00733 | hp2 | a0001 | c0001 | t0021 | g0272 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0090 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0286 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG00741 | hp2 | a0001 | c0001 | t0065 | g0020 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01069 | hp2 | a0001 | c0001 | t0023 | g0001 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01071 | hp2 | a0001 | c0001 | t0023 | g0001 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0082 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01081 | hp1 | a0001 | c0001 | t0072 | g0209 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0241 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01109 | hp1 | a0001 | c0001 | t0025 | g0108 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01167 | hp1 | a0001 | c0001 | t0073 | g0053 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0314 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01243 | hp1 | a0001 | c0001 | t0022 | g0032 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01243 | hp2 | a0001 | c0001 | t0032 | g0324 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01256 | hp1 | a0001 | c0001 | t0014 | g0198 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01257 | hp1 | a0001 | c0001 | t0062 | g0313 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0332 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01258 | hp1 | a0001 | c0001 | t0014 | g0234 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01258 | hp2 | a0001 | c0001 | t0031 | g0196 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0116 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01346 | hp2 | a0001 | c0001 | t0028 | g0018 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01358 | hp1 | a0001 | c0001 | t0061 | g0250 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0030 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01496 | hp2 | a0001 | c0001 | t0015 | g0117 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01515 | hp1 | a0003 | c0007 | t0001 | g0052 | EUR | IBS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01884 | hp1 | a0002 | c0006 | t0010 | g0112 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0192 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0205 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01934 | hp1 | a0001 | c0001 | t0021 | g0262 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01943 | hp2 | a0001 | c0001 | t0009 | g0226 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0311 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0229 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02015 | hp1 | a0001 | c0001 | t0047 | g0025 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02040 | hp1 | a0001 | c0001 | t0011 | g0166 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02055 | hp1 | a0001 | c0001 | t0019 | g0330 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02055 | hp2 | a0001 | c0001 | t0024 | g0107 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02056 | hp2 | a0001 | c0001 | t0069 | g0301 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0122 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0317 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02148 | hp1 | a0001 | c0001 | t0009 | g0284 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0312 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | CDX | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | CDX | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02257 | hp1 | a0001 | c0001 | t0050 | g0024 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0326 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0328 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02273 | hp1 | a0001 | c0001 | t0009 | g0227 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02280 | hp2 | a0001 | c0001 | t0043 | g0103 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02293 | hp1 | a0001 | c0001 | t0026 | g0191 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02293 | hp2 | a0001 | c0001 | t0079 | g0228 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02300 | hp1 | a0001 | c0001 | t0026 | g0059 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0230 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02523 | hp1 | a0001 | c0001 | t0067 | g0277 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02572 | hp1 | a0001 | c0001 | t0041 | g0091 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02572 | hp2 | a0001 | c0001 | t0056 | g0141 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0086 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02615 | hp1 | a0001 | c0001 | t0017 | g0098 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02615 | hp2 | a0001 | c0001 | t0031 | g0195 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02622 | hp1 | a0001 | c0002 | t0048 | g0298 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02630 | hp2 | a0001 | c0001 | t0040 | g0007 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02647 | hp1 | a0001 | c0001 | t0029 | g0083 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02647 | hp2 | a0001 | c0001 | t0018 | g0081 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0039 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0088 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02698 | hp1 | a0001 | c0001 | t0014 | g0266 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0138 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0322 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02809 | hp1 | a0001 | c0001 | t0037 | g0304 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0101 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02818 | hp2 | a0001 | c0001 | t0032 | g0325 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0329 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02886 | hp2 | a0001 | c0001 | t0053 | g0321 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02895 | hp2 | a0001 | c0001 | t0030 | g0331 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02896 | hp2 | a0001 | c0001 | t0030 | g0073 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02922 | hp2 | a0001 | c0001 | t0012 | g0076 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0077 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02965 | hp2 | a0001 | c0001 | t0046 | g0133 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0115 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02970 | hp2 | a0001 | c0001 | t0017 | g0100 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0099 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02976 | hp2 | a0001 | c0001 | t0052 | g0220 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03041 | hp1 | a0001 | c0001 | t0027 | g0067 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03098 | hp1 | a0001 | c0001 | t0060 | g0302 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0327 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03130 | hp2 | a0001 | c0001 | t0070 | g0134 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03139 | hp1 | a0001 | c0001 | t0045 | g0104 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03139 | hp2 | a0001 | c0001 | t0042 | g0092 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03195 | hp2 | a0001 | c0001 | t0054 | g0022 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03209 | hp2 | a0001 | c0001 | t0025 | g0087 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03453 | hp1 | a0001 | c0001 | t0020 | g0065 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03486 | hp1 | a0001 | c0001 | t0019 | g0323 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03486 | hp2 | a0001 | c0001 | t0057 | g0208 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03490 | hp1 | a0001 | c0001 | t0013 | g0006 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03490 | hp2 | a0001 | c0003 | t0011 | g0260 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03491 | hp2 | a0001 | c0001 | t0008 | g0043 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03492 | hp1 | a0001 | c0003 | t0011 | g0261 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0042 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03540 | hp2 | a0001 | c0001 | t0039 | g0102 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03579 | hp2 | a0001 | c0008 | t0071 | g0068 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03654 | hp1 | a0001 | c0001 | t0059 | g0033 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03669 | hp2 | a0001 | c0001 | t0066 | g0027 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03688 | hp1 | a0001 | c0001 | t0058 | g0315 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03710 | hp1 | a0001 | c0001 | t0013 | g0239 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03710 | hp2 | a0001 | c0001 | t0013 | g0005 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03831 | hp1 | a0001 | c0001 | t0035 | g0303 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03831 | hp2 | a0001 | c0001 | t0014 | g0259 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0158 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03927 | hp1 | a0001 | c0001 | t0078 | g0316 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0203 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0319 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0111 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG04184 | hp1 | a0001 | c0005 | t0001 | g0293 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0089 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG04199 | hp1 | a0001 | c0009 | t0002 | g0186 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG04204 | hp1 | a0001 | c0001 | t0075 | g0008 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG04228 | hp1 | a0001 | c0001 | t0010 | g0063 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0072 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18522 | hp2 | a0001 | c0001 | t0019 | g0069 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | CHB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18906 | hp1 | a0001 | c0001 | t0024 | g0106 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0071 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0154 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18962 | hp1 | a0001 | c0001 | t0028 | g0242 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18968 | hp2 | a0001 | c0001 | t0011 | g0204 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18977 | hp2 | a0001 | c0001 | t0077 | g0254 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18983 | hp2 | a0001 | c0001 | t0081 | g0136 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18985 | hp2 | a0001 | c0001 | t0063 | g0273 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18993 | hp1 | a0001 | c0001 | t0033 | g0212 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18994 | hp1 | a0001 | c0001 | t0055 | g0318 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18998 | hp2 | a0001 | c0001 | t0013 | g0249 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0096 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19030 | hp2 | a0001 | c0001 | t0027 | g0299 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19043 | hp2 | a0001 | c0001 | t0038 | g0109 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19062 | hp2 | a0001 | c0001 | t0074 | g0211 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19065 | hp2 | a0001 | c0001 | t0068 | g0013 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19084 | hp2 | a0001 | c0001 | t0080 | g0187 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0074 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA19240 | hp2 | a0001 | c0001 | t0044 | g0093 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA20129 | hp1 | a0001 | c0001 | t0051 | g0207 | AFR | ASW | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | ASW | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0159 | EUR | TSI | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA20805 | hp2 | a0001 | c0001 | t0022 | g0055 | EUR | TSI | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0110 | SAS | GIH | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | GIH | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01123 | hp1 | a0001 | c0001 | t0022 | g0051 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02109 | hp1 | a0001 | c0002 | t0018 | g0114 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0097 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02486 | hp1 | a0001 | c0001 | t0049 | g0320 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02486 | hp2 | a0001 | c0001 | t0029 | g0144 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02559 | hp1 | a0001 | c0001 | t0036 | g0094 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG02559 | hp2 | a0001 | c0001 | t0020 | g0064 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0118 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG03471 | hp2 | a0001 | c0001 | t0020 | g0066 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG06807 | hp1 | a0001 | c0001 | t0018 | g0084 | AFR | USA | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| HG06807 | hp2 | a0001 | c0001 | t0034 | g0105 | AFR | USA | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18955 | hp1 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA20300 | hp1 | a0001 | c0001 | t0064 | g0147 | AFR | USA | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA20300 | hp2 | a0001 | c0001 | t0016 | g0075 | AFR | USA | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0070 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0157 | REF | REF | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0177 | REF | REF | AGPAT3_chr21_43860223_43992592 | AGPAT3 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43971391
|
C | T | 1 | a0003 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.668C>T | p.Ala223Val | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/10 | 902/6565 | 668/1131 | 223/376 | chr21 | 43971391 | ||
| chr21:43981031
|
G | A | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.886G>A | p.Gly296Arg | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1120/6565 | 886/1131 | 296/376 | chr21 | 43981031 | ||
| chr21:43981041
|
T | G | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.896T>G | p.Phe299Cys | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1130/6565 | 896/1131 | 299/376 | chr21 | 43981041 | ||
| chr21:43981042
|
T | G | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.897T>G | p.Phe299Leu | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1131/6565 | 897/1131 | 299/376 | chr21 | 43981042 | ||
| chr21:43981059
|
C | A | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.914C>A | p.Pro305Gln | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1148/6565 | 914/1131 | 305/376 | chr21 | 43981059 | ||
| chr21:43981061
|
T | G | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.916T>G | p.Trp306Gly | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1150/6565 | 916/1131 | 306/376 | chr21 | 43981061 | ||
| chr21:43981065
|
C | G | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.920C>G | p.Thr307Ser | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1154/6565 | 920/1131 | 307/376 | chr21 | 43981065 | ||
| chr21:43981068
|
T | G | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.923T>G | p.Leu308Arg | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1157/6565 | 923/1131 | 308/376 | chr21 | 43981068 | ||
| chr21:43981091
|
A | G | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.946A>G | p.Thr316Ala | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1180/6565 | 946/1131 | 316/376 | chr21 | 43981091 | ||
| chr21:43981092
|
C | A | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.947C>A | p.Thr316Asn | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1181/6565 | 947/1131 | 316/376 | chr21 | 43981092 | ||
| chr21:43981103
|
T | A | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.958T>A | p.Ser320Thr | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1192/6565 | 958/1131 | 320/376 | chr21 | 43981103 | ||
| chr21:43981133
|
T | C | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.988T>C | p.Phe330Leu | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1222/6565 | 988/1131 | 330/376 | chr21 | 43981133 | ||
| chr21:43981134
|
T | C | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.989T>C | p.Phe330Ser | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1223/6565 | 989/1131 | 330/376 | chr21 | 43981134 | ||
| chr21:43981136
|
G | T | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.991G>T | p.Ala331Ser | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1225/6565 | 991/1131 | 331/376 | chr21 | 43981136 | ||
| chr21:43981140
|
G | T | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.995G>T | p.Ser332Ile | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1229/6565 | 995/1131 | 332/376 | chr21 | 43981140 | ||
| chr21:43981155
|
T | A | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1010T>A | p.Leu337Gln | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1244/6565 | 1010/1131 | 337/376 | chr21 | 43981155 | ||
| chr21:43981167
|
T | C | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1022T>C | p.Phe341Ser | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1256/6565 | 1022/1131 | 341/376 | chr21 | 43981167 | ||
| chr21:43981170
|
T | G | 1 | a0002 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1025T>G | p.Leu342Trp | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1259/6565 | 1025/1131 | 342/376 | chr21 | 43981170 | ||
| chr21:43981185
|
C | A | 1 | a0002 | 1 | HG01884.hp1 | missense_variant&splice_region_variant | MODERATE | c.1040C>A | p.Ala347Glu | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1274/6565 | 1040/1131 | 347/376 | chr21 | 43981185 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43959714
|
C | T | 1 | a0001c0009 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.33C>T | p.Phe11Phe | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/10 | 267/6565 | 33/1131 | 11/376 | chr21 | 43959714 | ||
| chr21:43969150
|
C | G | 1 | a0001c0008 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.381C>G | p.Leu127Leu | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/10 | 615/6565 | 381/1131 | 127/376 | chr21 | 43969150 | ||
| chr21:43969153
|
C | T | 1 | a0001c0003 | 2 | HG03490.hp2 HG03492.hp1 |
synonymous_variant | LOW | c.384C>T | p.Tyr128Tyr | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/10 | 618/6565 | 384/1131 | 128/376 | chr21 | 43969153 | ||
| chr21:43969159
|
C | T | 1 | a0001c0002 | 2 | HG02109.hp1 HG02622.hp1 |
synonymous_variant | LOW | c.390C>T | p.Pro130Pro | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/10 | 624/6565 | 390/1131 | 130/376 | chr21 | 43969159 | ||
| chr21:43969258
|
G | A | 1 | a0001c0004 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.489G>A | p.Ser163Ser | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/10 | 723/6565 | 489/1131 | 163/376 | chr21 | 43969258 | ||
| chr21:43970760
|
G | A | 1 | a0001c0005 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.618G>A | p.Pro206Pro | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/10 | 852/6565 | 618/1131 | 206/376 | chr21 | 43970760 | ||
| chr21:43981030
|
A | C | 1 | a0002c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.885A>C | p.Pro295Pro | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1119/6565 | 885/1131 | 295/376 | chr21 | 43981030 | ||
| chr21:43981033
|
G | T | 1 | a0002c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.888G>T | p.Gly296Gly | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1122/6565 | 888/1131 | 296/376 | chr21 | 43981033 | ||
| chr21:43981069
|
C | T | 1 | a0002c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.924C>T | p.Leu308Leu | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1158/6565 | 924/1131 | 308/376 | chr21 | 43981069 | ||
| chr21:43981132
|
C | G | 1 | a0002c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.987C>G | p.Val329Val | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1221/6565 | 987/1131 | 329/376 | chr21 | 43981132 | ||
| chr21:43981159
|
C | T | 1 | a0002c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1014C>T | p.Ile338Ile | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1248/6565 | 1014/1131 | 338/376 | chr21 | 43981159 | ||
| chr21:43981168
|
C | T | 1 | a0002c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1023C>T | p.Phe341Phe | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1257/6565 | 1023/1131 | 341/376 | chr21 | 43981168 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43903982
|
G | A | 21 | a0001c0001t0005a0001c0001t0010a0001c0001t0012others(18): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/10 | 55700 | chr21 | 43903982 | |||||
| chr21:43959679
|
G | A | 1 | a0001c0001t0026 | 2 | HG02293.hp1 HG02300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-3G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/10 | 3 | chr21 | 43959679 | |||||
| chr21:43982507
|
A | T | 1 | a0001c0001t0081 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 115 | chr21 | 43982507 | |||||
| chr21:43982604
|
C | T | 1 | a0001c0001t0080 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*212C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 212 | chr21 | 43982604 | |||||
| chr21:43982680
|
G | C | 1 | a0001c0001t0034 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*288G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 288 | chr21 | 43982680 | |||||
| chr21:43982867
|
C | T | 1 | a0001c0001t0079 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*475C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 475 | chr21 | 43982867 | |||||
| chr21:43982935
|
G | A | 1 | a0001c0001t0046 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*543G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 543 | chr21 | 43982935 | |||||
| chr21:43982939
|
G | A | 32 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(29): Show | 88 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*547G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 547 | chr21 | 43982939 | |||||
| chr21:43983133
|
C | A | 1 | a0001c0001t0058 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*741C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 741 | chr21 | 43983133 | |||||
| chr21:43983221
|
C | T | 2 | a0001c0001t0041a0001c0001t0057 | 2 | HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*829C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 829 | chr21 | 43983221 | |||||
| chr21:43983351
|
A | G | 5 | a0001c0001t0003a0001c0001t0007a0001c0001t0040others(2): Show | 38 | HG00544.hp2 HG00597.hp2 HG01891.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*959A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 959 | chr21 | 43983351 | |||||
| chr21:43983477
|
A | G | 48 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(45): Show | 164 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*1085A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1085 | chr21 | 43983477 | |||||
| chr21:43983527
|
C | T | 2 | a0001c0001t0046a0001c0001t0070 | 2 | HG02965.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1135C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1135 | chr21 | 43983527 | |||||
| chr21:43983665
|
A | G | 3 | a0001c0001t0008a0001c0001t0011a0001c0003t0011 | 11 | HG00323.hp2 HG02040.hp1 HG02683.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1273A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1273 | chr21 | 43983665 | |||||
| chr21:43983679
|
G | A | 4 | a0001c0001t0024a0001c0001t0034a0001c0001t0043others(1): Show | 5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1287G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1287 | chr21 | 43983679 | |||||
| chr21:43983779
|
T | C | 1 | a0001c0001t0059 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1387T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1387 | chr21 | 43983779 | |||||
| chr21:43984007
|
C | T | 1 | a0001c0001t0069 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1615C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1615 | chr21 | 43984007 | |||||
| chr21:43984048
|
C | T | 4 | a0001c0001t0036a0001c0001t0037a0001c0001t0038others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1656C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1656 | chr21 | 43984048 | |||||
| chr21:43984146
|
T | C | 1 | a0001c0001t0024 | 2 | HG02055.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1754T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1754 | chr21 | 43984146 | |||||
| chr21:43984239
|
C | T | 37 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(34): Show | 117 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1847C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1847 | chr21 | 43984239 | |||||
| chr21:43984242
|
G | A | 2 | a0001c0001t0015a0001c0001t0072 | 5 | HG01081.hp1 HG01261.hp2 HG01496.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1850G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1850 | chr21 | 43984242 | |||||
| chr21:43984379
|
A | G | 1 | a0001c0001t0067 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1987A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1987 | chr21 | 43984379 | |||||
| chr21:43984457
|
A | G | 44 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(41): Show | 127 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2065A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2065 | chr21 | 43984457 | |||||
| chr21:43984681
|
AT | A | 25 | a0001c0001t0008a0001c0001t0011a0001c0001t0012others(22): Show | 46 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2301delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2301 | INFO_REALIGN_3_PRIME | chr21 | 43984681 | ||||
| chr21:43984681
|
ATT | A | 5 | a0001c0001t0015a0001c0001t0025a0001c0001t0036others(2): Show | 9 | HG01081.hp1 HG01109.hp1 HG01261.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2300_*2301delTT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2300 | INFO_REALIGN_3_PRIME | chr21 | 43984681 | ||||
| chr21:43984693
|
T | G | 3 | a0001c0001t0015a0001c0001t0025a0001c0001t0072 | 7 | HG01081.hp1 HG01109.hp1 HG01261.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2301T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2301 | chr21 | 43984693 | |||||
| chr21:43984696
|
G | C | 1 | a0001c0001t0061 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2304G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2304 | chr21 | 43984696 | |||||
| chr21:43984756
|
A | G | 2 | a0001c0001t0046a0001c0001t0070 | 2 | HG02965.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2364A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2364 | chr21 | 43984756 | |||||
| chr21:43984791
|
C | CT | 23 | a0001c0001t0002a0001c0001t0004a0001c0001t0016others(20): Show | 89 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2409dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2410 | INFO_REALIGN_3_PRIME | chr21 | 43984791 | ||||
| chr21:43984805
|
T | C | 2 | a0001c0001t0030a0001c0001t0051 | 3 | HG02895.hp2 HG02896.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2413T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2413 | chr21 | 43984805 | |||||
| chr21:43984965
|
A | G | 21 | a0001c0001t0008a0001c0001t0011a0001c0001t0015others(18): Show | 38 | HG00323.hp2 HG01081.hp1 HG01109.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2573A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2573 | chr21 | 43984965 | |||||
| chr21:43984982
|
G | A | 1 | a0001c0002t0048 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2590G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2590 | chr21 | 43984982 | |||||
| chr21:43985086
|
G | A | 1 | a0001c0001t0051 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2694G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2694 | chr21 | 43985086 | |||||
| chr21:43985093
|
C | A | 20 | a0001c0001t0008a0001c0001t0011a0001c0001t0015others(17): Show | 37 | HG00323.hp2 HG01081.hp1 HG01109.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2701C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2701 | chr21 | 43985093 | |||||
| chr21:43985228
|
C | A | 1 | a0001c0001t0060 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2836 | chr21 | 43985228 | |||||
| chr21:43985275
|
C | T | 1 | a0001c0001t0047 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2883C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2883 | chr21 | 43985275 | |||||
| chr21:43985337
|
T | G | 1 | a0001c0001t0009 | 6 | HG01358.hp2 HG01943.hp2 HG01981.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2945T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2945 | chr21 | 43985337 | |||||
| chr21:43985342
|
G | A | 1 | a0001c0001t0076 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2950G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2950 | chr21 | 43985342 | |||||
| chr21:43985397
|
T | TA | 25 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(22): Show | 76 | HG00323.hp2 HG01167.hp2 HG01243.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*3020dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3021 | INFO_REALIGN_3_PRIME | chr21 | 43985397 | ||||
| chr21:43985565
|
C | G | 1 | a0001c0001t0078 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3173C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3173 | chr21 | 43985565 | |||||
| chr21:43985665
|
G | C | 16 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(13): Show | 62 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*3273G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3273 | chr21 | 43985665 | |||||
| chr21:43986048
|
T | C | 1 | a0001c0001t0027 | 2 | HG03041.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3656T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3656 | chr21 | 43986048 | |||||
| chr21:43986144
|
G | C | 1 | a0001c0001t0063 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3752G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3752 | chr21 | 43986144 | |||||
| chr21:43986162
|
A | G | 1 | a0001c0001t0044 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3770A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3770 | chr21 | 43986162 | |||||
| chr21:43986214
|
C | G | 54 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(51): Show | 178 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*3822C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3822 | chr21 | 43986214 | |||||
| chr21:43986313
|
A | G | 1 | a0001c0001t0065 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3921A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3921 | chr21 | 43986313 | |||||
| chr21:43986722
|
G | C | 4 | a0001c0001t0036a0001c0001t0037a0001c0001t0038others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4330G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4330 | chr21 | 43986722 | |||||
| chr21:43986739
|
T | G | 1 | a0001c0001t0056 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4347T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4347 | chr21 | 43986739 | |||||
| chr21:43986740
|
T | G | 1 | a0001c0001t0056 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4348T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4348 | chr21 | 43986740 | |||||
| chr21:43986800
|
T | C | 1 | a0001c0001t0047 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4408T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4408 | chr21 | 43986800 | |||||
| chr21:43986939
|
C | G | 1 | a0001c0001t0014 | 4 | HG01256.hp1 HG01258.hp1 HG02698.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4547C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4547 | chr21 | 43986939 | |||||
| chr21:43986939
|
C | T | 1 | a0001c0001t0019 | 3 | HG02055.hp1 HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4547C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4547 | chr21 | 43986939 | |||||
| chr21:43986995
|
T | C | 3 | a0001c0001t0033a0001c0001t0074a0001c0001t0077 | 4 | HG00558.hp2 NA18977.hp2 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4603T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4603 | chr21 | 43986995 | |||||
| chr21:43986997
|
C | T | 1 | a0001c0001t0015 | 4 | HG01261.hp2 HG01496.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4605C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4605 | chr21 | 43986997 | |||||
| chr21:43987033
|
C | T | 1 | a0001c0001t0064 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4641C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4641 | chr21 | 43987033 | |||||
| chr21:43987038
|
G | A | 1 | a0001c0001t0038 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4646G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4646 | chr21 | 43987038 | |||||
| chr21:43987154
|
T | C | 2 | a0001c0001t0021a0001c0001t0079 | 4 | HG00323.hp1 HG00733.hp2 HG01934.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4762T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4762 | chr21 | 43987154 | |||||
| chr21:43987415
|
C | A | 3 | a0001c0001t0015a0001c0001t0025a0001c0001t0072 | 7 | HG01081.hp1 HG01109.hp1 HG01261.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5023C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 5023 | chr21 | 43987415 | |||||
| chr21:43987439
|
T | G | 3 | a0001c0001t0020a0001c0001t0042a0001c0001t0060 | 5 | HG02559.hp2 HG03098.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5047T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 5047 | chr21 | 43987439 | |||||
| chr21:43987491
|
A | T | 1 | a0001c0001t0019 | 3 | HG02055.hp1 HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5099A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 5099 | chr21 | 43987491 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43865390
|
C | T | 9 | a0001c0001t0001g0334a0001c0001t0002g0332a0001c0001t0002g0333others(6): Show | 9 | HG01257.hp2 NA18973.hp1 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.-112+45C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865390 | ||||||
| chr21:43865557
|
G | C | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG01192.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-112+212G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865557 | ||||||
| chr21:43865575
|
G | T | 9 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-112+230G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865575 | ||||||
| chr21:43865635
|
G | T | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-112+290G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865635 | ||||||
| chr21:43865830
|
C | G | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-112+485C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865830 | ||||||
| chr21:43865835
|
A | AC | 23 | a0001c0001t0001g0300a0001c0001t0001g0305a0001c0001t0001g0309others(20): Show | 23 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.-112+498dupC | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43865835 | |||||
| chr21:43865837
|
C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+492C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865837 | ||||||
| chr21:43865937
|
G | A | 2 | a0001c0001t0013g0005a0001c0001t0013g0006 | 2 | HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-112+592G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865937 | ||||||
| chr21:43865940
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-112+595C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865940 | ||||||
| chr21:43865945
|
C | G | 2 | a0001c0001t0002g0296a0001c0001t0003g0319 | 2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-112+600C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865945 | ||||||
| chr21:43865952
|
C | G | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG01981.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-112+607C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865952 | ||||||
| chr21:43865969
|
C | T | 1 | a0001c0005t0001g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-112+624C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865969 | ||||||
| chr21:43866079
|
G | T | 1 | a0001c0001t0001g0292 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-112+734G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866079 | ||||||
| chr21:43866120
|
G | GT | 22 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0201others(19): Show | 22 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-112+792dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43866120 | |||||
| chr21:43866120
|
G | GTT | 83 | a0001c0001t0001g0206a0001c0001t0001g0210a0001c0001t0001g0214others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-112+791_-112+792d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43866120 | |||||
| chr21:43866120
|
G | GTTT | 21 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0285others(18): Show | 21 | HG00741.hp1 HG01243.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.-112+790_-112+792d others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43866120 | |||||
| chr21:43866199
|
T | TA | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-112+866dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43866199 | |||||
| chr21:43866396
|
G | A | 1 | a0001c0001t0010g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-112+1051G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866396 | ||||||
| chr21:43866407
|
C | G | 1 | a0001c0001t0010g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-112+1062C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866407 | ||||||
| chr21:43866457
|
G | A | 5 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(2): Show | 5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112+1112G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866457 | ||||||
| chr21:43866553
|
G | A | 1 | a0001c0001t0002g0332 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-112+1208G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866553 | ||||||
| chr21:43866682
|
T | C | 2 | a0001c0001t0007g0192a0001c0001t0053g0321 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-112+1337T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866682 | ||||||
| chr21:43866684
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-112+1339C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866684 | ||||||
| chr21:43866768
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-112+1423C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866768 | ||||||
| chr21:43867403
|
G | A | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-112+2058G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867403 | ||||||
| chr21:43867458
|
G | A | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+2113G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867458 | ||||||
| chr21:43867620
|
C | T | 99 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-112+2275C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867620 | ||||||
| chr21:43867632
|
C | G | 1 | a0001c0009t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-112+2287C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867632 | ||||||
| chr21:43867649
|
A | G | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-112+2304A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867649 | ||||||
| chr21:43867723
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0074g0211 | 2 | NA18977.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-112+2378T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867723 | ||||||
| chr21:43867739
|
G | A | 6 | a0001c0001t0006g0074a0001c0001t0012g0070a0001c0001t0016g0071others(3): Show | 6 | HG02896.hp2 NA18522.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112+2394G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867739 | ||||||
| chr21:43867746
|
T | C | 1 | a0001c0001t0012g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-112+2401T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867746 | ||||||
| chr21:43867884
|
GTGTT | G | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+2542_-112+254 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43867884 | |||||
| chr21:43867935
|
G | A | 1 | a0001c0001t0017g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-112+2590G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867935 | ||||||
| chr21:43868172
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-112+2827G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43868172 | ||||||
| chr21:43868622
|
G | C | 1 | a0001c0001t0004g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-112+3277G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43868622 | ||||||
| chr21:43868893
|
G | A | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-112+3548G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43868893 | ||||||
| chr21:43869277
|
T | C | 1 | a0001c0001t0003g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-112+3932T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869277 | ||||||
| chr21:43869343
|
A | G | 6 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(3): Show | 6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+3998A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869343 | ||||||
| chr21:43869368
|
G | T | 1 | a0001c0001t0004g0185 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-112+4023G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869368 | ||||||
| chr21:43869651
|
C | T | 6 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0184others(3): Show | 6 | HG02074.hp2 NA18974.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+4306C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869651 | ||||||
| chr21:43869817
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-112+4472C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869817 | ||||||
| chr21:43869819
|
T | C | 260 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(257): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.-112+4474T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869819 | ||||||
| chr21:43869903
|
A | G | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-112+4558A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869903 | ||||||
| chr21:43869932
|
T | C | 333 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(330): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-112+4587T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869932 | ||||||
| chr21:43870091
|
C | T | 2 | a0001c0001t0002g0171a0001c0001t0067g0277 | 2 | HG02523.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-112+4746C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870091 | ||||||
| chr21:43870232
|
C | T | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+4887C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870232 | ||||||
| chr21:43870310
|
G | A | 12 | a0001c0001t0001g0210a0001c0001t0001g0214a0001c0001t0001g0215others(9): Show | 12 | HG00558.hp2 HG00621.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-112+4965G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870310 | ||||||
| chr21:43870324
|
T | A | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+4979T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870324 | ||||||
| chr21:43870329
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0294a0001c0001t0001g0295others(4): Show | 7 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112+4984G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870329 | ||||||
| chr21:43870550
|
T | TA | 8 | a0001c0001t0002g0078a0001c0001t0002g0120a0001c0001t0003g0119others(5): Show | 8 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-112+5220dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43870550 | |||||
| chr21:43870563
|
A | C | 201 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-112+5218A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870563 | ||||||
| chr21:43870591
|
C | T | 1 | a0001c0001t0006g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-112+5246C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870591 | ||||||
| chr21:43870608
|
G | T | 6 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(3): Show | 6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+5263G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870608 | ||||||
| chr21:43870915
|
T | C | 208 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-112+5570T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870915 | ||||||
| chr21:43871072
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-112+5727G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871072 | ||||||
| chr21:43871086
|
G | C | 2 | a0001c0001t0005g0082a0001c0001t0035g0303 | 2 | HG01074.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-112+5741G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871086 | ||||||
| chr21:43871175
|
A | C | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0276 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-112+5830A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871175 | ||||||
| chr21:43871218
|
G | A | 101 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(98): Show | 101 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-112+5873G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871218 | ||||||
| chr21:43871319
|
G | T | 4 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112+5974G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871319 | ||||||
| chr21:43871445
|
A | T | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-112+6100A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871445 | ||||||
| chr21:43871582
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-112+6237G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871582 | ||||||
| chr21:43872071
|
G | A | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-112+6726G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872071 | ||||||
| chr21:43872178
|
G | GT | 20 | a0001c0001t0001g0274a0001c0001t0002g0060a0001c0001t0003g0167others(17): Show | 20 | HG01261.hp2 HG01496.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-112+6848dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43872178 | |||||
| chr21:43872253
|
T | G | 199 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.-112+6908T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872253 | ||||||
| chr21:43872425
|
C | T | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-112+7080C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872425 | ||||||
| chr21:43872785
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-112+7440T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872785 | ||||||
| chr21:43872866
|
A | G | 3 | a0001c0001t0015g0116a0001c0001t0015g0117a0001c0001t0015g0118 | 3 | HG01261.hp2 HG01496.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-112+7521A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872866 | ||||||
| chr21:43872908
|
C | T | 5 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(2): Show | 5 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112+7563C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872908 | ||||||
| chr21:43872957
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0026g0059others(1): Show | 4 | HG02293.hp1 HG02300.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+7612C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872957 | ||||||
| chr21:43872983
|
C | T | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+7638C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872983 | ||||||
| chr21:43872998
|
G | A | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-112+7653G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872998 | ||||||
| chr21:43873074
|
G | A | 6 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(3): Show | 6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+7729G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873074 | ||||||
| chr21:43873136
|
C | T | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-112+7791C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873136 | ||||||
| chr21:43873148
|
G | C | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-112+7803G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873148 | ||||||
| chr21:43873162
|
G | C | 1 | a0001c0001t0027g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-112+7817G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873162 | ||||||
| chr21:43873312
|
G | A | 1 | a0001c0009t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-112+7967G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873312 | ||||||
| chr21:43873321
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0021g0272 | 2 | HG00733.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-112+7976C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873321 | ||||||
| chr21:43873386
|
C | T | 1 | a0001c0001t0010g0110 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-112+8041C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873386 | ||||||
| chr21:43873480
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-112+8135C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873480 | ||||||
| chr21:43873481
|
G | A | 2 | a0001c0001t0007g0192a0001c0001t0053g0321 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-112+8136G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873481 | ||||||
| chr21:43873522
|
C | T | 1 | a0001c0001t0019g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-112+8177C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873522 | ||||||
| chr21:43873524
|
C | T | 203 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-112+8179C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873524 | ||||||
| chr21:43873569
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG01981.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-112+8224G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873569 | ||||||
| chr21:43873680
|
A | G | 107 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-112+8335A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873680 | ||||||
| chr21:43873850
|
C | T | 123 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(120): Show | 123 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-112+8505C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873850 | ||||||
| chr21:43874077
|
G | A | 16 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(13): Show | 17 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-112+8732G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874077 | ||||||
| chr21:43874086
|
C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+8741C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874086 | ||||||
| chr21:43874112
|
G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+8767G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874112 | ||||||
| chr21:43874118
|
C | T | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-112+8773C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874118 | ||||||
| chr21:43874261
|
G | A | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+8916G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874261 | ||||||
| chr21:43874263
|
C | T | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+8918C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874263 | ||||||
| chr21:43874264
|
A | G | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+8919A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874264 | ||||||
| chr21:43874281
|
T | C | 259 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.-112+8936T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874281 | ||||||
| chr21:43874317
|
C | T | 204 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-112+8972C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874317 | ||||||
| chr21:43874336
|
C | G | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-112+8991C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874336 | ||||||
| chr21:43874400
|
G | A | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+9055G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874400 | ||||||
| chr21:43874519
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-112+9174G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874519 | ||||||
| chr21:43874616
|
C | T | 101 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(98): Show | 101 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-112+9271C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874616 | ||||||
| chr21:43874722
|
C | T | 1 | a0001c0001t0076g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-112+9377C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874722 | ||||||
| chr21:43874850
|
T | TC | 6 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(3): Show | 6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+9506dupC | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43874850 | |||||
| chr21:43875043
|
C | T | 1 | a0001c0001t0003g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-112+9698C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875043 | ||||||
| chr21:43875066
|
C | T | 1 | a0001c0001t0002g0171 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-112+9721C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875066 | ||||||
| chr21:43875080
|
A | G | 92 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(89): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-112+9735A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875080 | ||||||
| chr21:43875230
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-112+9885C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875230 | ||||||
| chr21:43875276
|
G | A | 205 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-112+9931G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875276 | ||||||
| chr21:43875389
|
C | T | 1 | a0001c0001t0004g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-112+10044C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875389 | ||||||
| chr21:43875469
|
C | T | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+10124C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875469 | ||||||
| chr21:43875646
|
T | C | 196 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-112+10301T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875646 | ||||||
| chr21:43875897
|
C | T | 99 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(96): Show | 99 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-112+10552C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875897 | ||||||
| chr21:43875907
|
C | A | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+10562C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875907 | ||||||
| chr21:43875940
|
G | GTTC | 3 | a0001c0001t0019g0069a0001c0001t0049g0320a0001c0008t0071g0068 | 3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+10598_-112+10 others(9): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43875940 | |||||
| chr21:43876114
|
G | A | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+10769G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876114 | ||||||
| chr21:43876269
|
G | A | 3 | a0001c0001t0001g0300a0001c0001t0004g0012a0001c0001t0068g0013 | 3 | HG00597.hp1 NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-112+10924G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876269 | ||||||
| chr21:43876287
|
T | C | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+10942T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876287 | ||||||
| chr21:43876347
|
C | A | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+11002C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876347 | ||||||
| chr21:43876802
|
G | A | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+11457G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876802 | ||||||
| chr21:43876868
|
T | G | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+11523T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876868 | ||||||
| chr21:43877066
|
C | T | 1 | a0001c0001t0022g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-112+11721C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877066 | ||||||
| chr21:43877102
|
G | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | HG01167.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-112+11757G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877102 | ||||||
| chr21:43877119
|
G | A | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+11774G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877119 | ||||||
| chr21:43877323
|
G | A | 1 | a0001c0001t0026g0191 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-112+11978G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877323 | ||||||
| chr21:43877529
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-112+12184G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877529 | ||||||
| chr21:43877686
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-112+12341C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877686 | ||||||
| chr21:43877690
|
C | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-112+12345C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877690 | ||||||
| chr21:43877785
|
C | A | 1 | a0001c0001t0010g0095 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-112+12440C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877785 | ||||||
| chr21:43878030
|
A | G | 50 | a0001c0001t0002g0078a0001c0001t0005g0082a0001c0001t0005g0086others(47): Show | 51 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.-112+12685A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878030 | ||||||
| chr21:43878084
|
G | A | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-112+12739G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878084 | ||||||
| chr21:43878104
|
C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+12759C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878104 | ||||||
| chr21:43878111
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-112+12766C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878111 | ||||||
| chr21:43878113
|
C | A | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+12768C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878113 | ||||||
| chr21:43878156
|
C | T | 2 | a0001c0001t0019g0069a0001c0001t0049g0320 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+12811C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878156 | ||||||
| chr21:43878260
|
C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-112+12915C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878260 | ||||||
| chr21:43878507
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-112+13162C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878507 | ||||||
| chr21:43878567
|
A | G | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+13222A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878567 | ||||||
| chr21:43878736
|
C | CT | 60 | a0001c0001t0001g0054a0001c0001t0001g0164a0001c0001t0001g0179others(57): Show | 61 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.-112+13406dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43878736 | |||||
| chr21:43878799
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-112+13454A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878799 | ||||||
| chr21:43878810
|
G | A | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+13465G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878810 | ||||||
| chr21:43878992
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-112+13647C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878992 | ||||||
| chr21:43879134
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-112+13789G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879134 | ||||||
| chr21:43879294
|
G | A | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-112+13949G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879294 | ||||||
| chr21:43879347
|
C | CA | 15 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(12): Show | 15 | HG01243.hp2 HG01346.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.-112+14028dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43879347 | |||||
| chr21:43879347
|
CA | C | 37 | a0001c0001t0001g0162a0001c0001t0001g0264a0001c0001t0001g0265others(34): Show | 37 | HG00741.hp2 HG01261.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.-112+14028delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43879347 | |||||
| chr21:43879347
|
CAA | C | 68 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-112+14027_-112+14 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43879347 | |||||
| chr21:43879347
|
CAAA | C | 54 | a0001c0001t0002g0015a0001c0001t0002g0056a0001c0001t0002g0060others(51): Show | 55 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-112+14026_-112+14 others(9): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43879347 | |||||
| chr21:43879504
|
C | T | 1 | a0001c0001t0004g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-112+14159C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879504 | ||||||
| chr21:43879516
|
G | A | 1 | a0001c0001t0033g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-112+14171G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879516 | ||||||
| chr21:43879557
|
G | T | 2 | a0001c0001t0001g0263a0001c0001t0002g0267 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-112+14212G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879557 | ||||||
| chr21:43879697
|
G | T | 48 | a0001c0001t0002g0078a0001c0001t0005g0082a0001c0001t0005g0086others(45): Show | 49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-112+14352G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879697 | ||||||
| chr21:43879766
|
G | A | 6 | a0001c0001t0012g0076a0001c0001t0012g0099a0001c0001t0012g0101others(3): Show | 6 | HG02615.hp1 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112+14421G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879766 | ||||||
| chr21:43879857
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-112+14512G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879857 | ||||||
| chr21:43879964
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0283 | 2 | HG02080.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-112+14619G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879964 | ||||||
| chr21:43879965
|
G | A | 3 | a0001c0001t0006g0097a0001c0001t0010g0095a0001c0001t0010g0096 | 3 | HG00639.hp1 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-112+14620G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879965 | ||||||
| chr21:43880038
|
T | C | 1 | a0001c0001t0047g0025 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-112+14693T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880038 | ||||||
| chr21:43880139
|
A | G | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+14794A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880139 | ||||||
| chr21:43880361
|
G | T | 2 | a0001c0001t0051g0207a0001c0001t0057g0208 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-112+15016G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880361 | ||||||
| chr21:43880531
|
G | A | 3 | a0001c0001t0006g0097a0001c0001t0010g0095a0001c0001t0010g0096 | 3 | HG00639.hp1 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-112+15186G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880531 | ||||||
| chr21:43880678
|
A | G | 1 | a0001c0001t0003g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-112+15333A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880678 | ||||||
| chr21:43880883
|
A | G | 1 | a0001c0001t0021g0262 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-112+15538A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880883 | ||||||
| chr21:43880944
|
G | A | 1 | a0001c0001t0028g0018 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-112+15599G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880944 | ||||||
| chr21:43880963
|
GA | G | 101 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(98): Show | 101 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-112+15619delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880963 | ||||||
| chr21:43881182
|
T | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0283a0001c0001t0002g0178 | 3 | HG02080.hp1 NA19002.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-112+15837T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43881182 | ||||||
| chr21:43881225
|
G | A | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+15880G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43881225 | ||||||
| chr21:43881444
|
G | A | 46 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(43): Show | 47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-112+16099G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43881444 | ||||||
| chr21:43881917
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-112+16572A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43881917 | ||||||
| chr21:43881978
|
A | C | 1 | a0001c0001t0001g0283 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-112+16633A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43881978 | ||||||
| chr21:43882033
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-112+16688G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882033 | ||||||
| chr21:43882068
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-112+16723G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882068 | ||||||
| chr21:43882102
|
C | A | 1 | a0001c0001t0066g0027 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-112+16757C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882102 | ||||||
| chr21:43882183
|
C | T | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+16838C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882183 | ||||||
| chr21:43882192
|
G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+16847G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882192 | ||||||
| chr21:43882356
|
C | G | 2 | a0001c0001t0001g0263a0001c0001t0002g0267 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-112+17011C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882356 | ||||||
| chr21:43882411
|
C | T | 6 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(3): Show | 6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+17066C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882411 | ||||||
| chr21:43882447
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-112+17102G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882447 | ||||||
| chr21:43882451
|
G | T | 2 | a0001c0001t0027g0299a0001c0001t0050g0024 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-112+17106G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882451 | ||||||
| chr21:43882573
|
A | G | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+17228A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882573 | ||||||
| chr21:43882611
|
G | A | 6 | a0001c0001t0009g0226a0001c0001t0009g0227a0001c0001t0009g0229others(3): Show | 6 | HG01943.hp2 HG01981.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+17266G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882611 | ||||||
| chr21:43882642
|
G | T | 2 | a0001c0001t0001g0263a0001c0001t0002g0267 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-112+17297G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882642 | ||||||
| chr21:43882643
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0002g0267 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-112+17298C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882643 | ||||||
| chr21:43882731
|
G | A | 45 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(42): Show | 46 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.-112+17386G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882731 | ||||||
| chr21:43883090
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-112+17745G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883090 | ||||||
| chr21:43883293
|
G | A | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-112+17948G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883293 | ||||||
| chr21:43883301
|
C | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | NA18747.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-112+17956C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883301 | ||||||
| chr21:43883662
|
C | T | 1 | a0001c0001t0003g0160 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-112+18317C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883662 | ||||||
| chr21:43883825
|
C | T | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+18480C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883825 | ||||||
| chr21:43883833
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0006g0061a0001c0001t0022g0051others(2): Show | 5 | HG01123.hp1 HG01167.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112+18488A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883833 | ||||||
| chr21:43883883
|
T | G | 1 | a0001c0001t0002g0016 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-112+18538T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883883 | ||||||
| chr21:43884000
|
G | A | 81 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-112+18655G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884000 | ||||||
| chr21:43884138
|
G | C | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+18793G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884138 | ||||||
| chr21:43884173
|
T | G | 339 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(336): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-112+18828T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884173 | ||||||
| chr21:43884191
|
A | G | 339 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(336): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-112+18846A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884191 | ||||||
| chr21:43884244
|
G | A | 1 | a0001c0001t0003g0127 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-112+18899G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884244 | ||||||
| chr21:43884293
|
T | C | 9 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(6): Show | 10 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-112+18948T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884293 | ||||||
| chr21:43884612
|
GGGGTGCC others(15): Show |
G | 7 | a0001c0001t0001g0009a0001c0001t0001g0294a0001c0001t0001g0295others(4): Show | 7 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112+19276_-112+19 others(28): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43884612 | |||||
| chr21:43884832
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0002g0267 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-111-19125T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884832 | ||||||
| chr21:43884871
|
C | A | 1 | a0001c0001t0013g0006 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-111-19086C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884871 | ||||||
| chr21:43885078
|
C | G | 2 | a0001c0001t0007g0192a0001c0001t0053g0321 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-111-18879C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885078 | ||||||
| chr21:43885133
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-111-18824C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885133 | ||||||
| chr21:43885214
|
G | A | 2 | a0001c0001t0013g0005a0001c0001t0013g0006 | 2 | HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-111-18743G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885214 | ||||||
| chr21:43885280
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-111-18677G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885280 | ||||||
| chr21:43885317
|
G | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-111-18640G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885317 | ||||||
| chr21:43885391
|
CT | C | 49 | a0001c0001t0004g0029a0001c0001t0005g0082a0001c0001t0005g0086others(46): Show | 50 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.-111-18551delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43885391 | |||||
| chr21:43885420
|
G | C | 1 | a0001c0001t0001g0231 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-111-18537G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885420 | ||||||
| chr21:43885482
|
G | A | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-18475G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885482 | ||||||
| chr21:43885824
|
T | G | 1 | a0001c0001t0002g0219 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-111-18133T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885824 | ||||||
| chr21:43885826
|
TGCAGGTG others(1): Show |
T | 94 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(91): Show | 94 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-111-18117_-111-18 others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43885826 | |||||
| chr21:43886020
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-111-17937C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886020 | ||||||
| chr21:43886211
|
C | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0009g0030 | 3 | HG01358.hp2 HG02523.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-111-17746C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886211 | ||||||
| chr21:43886219
|
T | G | 90 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(87): Show | 90 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-111-17738T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886219 | ||||||
| chr21:43886226
|
T | C | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-111-17731T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886226 | ||||||
| chr21:43886238
|
A | G | 3 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0030g0331 | 3 | HG02055.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-111-17719A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886238 | ||||||
| chr21:43886249
|
T | C | 7 | a0001c0001t0003g0125a0001c0001t0003g0128a0001c0001t0003g0129others(4): Show | 7 | NA18941.hp2 NA18942.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-111-17708T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886249 | ||||||
| chr21:43886263
|
T | A | 47 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(44): Show | 48 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.-111-17694T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886263 | ||||||
| chr21:43886532
|
A | G | 48 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(45): Show | 49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-17425A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886532 | ||||||
| chr21:43886582
|
T | A | 39 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0132others(36): Show | 40 | HG00544.hp2 HG01261.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-17375T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886582 | ||||||
| chr21:43886793
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0023others(3): Show | 6 | HG01167.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-17164C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886793 | ||||||
| chr21:43886841
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0028g0018 | 2 | HG01346.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-111-17116C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886841 | ||||||
| chr21:43886900
|
T | C | 48 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(45): Show | 49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-17057T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886900 | ||||||
| chr21:43887027
|
T | C | 1 | a0001c0001t0029g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-111-16930T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887027 | ||||||
| chr21:43887058
|
C | T | 2 | a0001c0001t0004g0029a0001c0001t0004g0047 | 2 | HG00733.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-111-16899C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887058 | ||||||
| chr21:43887104
|
C | T | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0056others(3): Show | 6 | HG02293.hp1 HG02300.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-16853C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887104 | ||||||
| chr21:43887144
|
C | T | 94 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-111-16813C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887144 | ||||||
| chr21:43887148
|
C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-111-16809C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887148 | ||||||
| chr21:43887341
|
G | A | 4 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-16616G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887341 | ||||||
| chr21:43887582
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-111-16375A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887582 | ||||||
| chr21:43887695
|
C | T | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-16262C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887695 | ||||||
| chr21:43887855
|
T | C | 2 | a0001c0001t0019g0323a0001c0001t0019g0330 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-111-16102T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887855 | ||||||
| chr21:43888054
|
T | A | 1 | a0001c0001t0005g0088 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-111-15903T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888054 | ||||||
| chr21:43888083
|
T | C | 48 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(45): Show | 49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-15874T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888083 | ||||||
| chr21:43888398
|
GAT | G | 289 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-111-15546_-111-15 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43888398 | |||||
| chr21:43888580
|
T | G | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-111-15377T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888580 | ||||||
| chr21:43888820
|
C | T | 2 | a0001c0001t0036g0094a0001c0001t0037g0304 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-111-15137C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888820 | ||||||
| chr21:43888914
|
G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-15043G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888914 | ||||||
| chr21:43888951
|
T | C | 133 | a0001c0001t0001g0113a0001c0001t0001g0142a0001c0001t0001g0164others(130): Show | 134 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-111-15006T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888951 | ||||||
| chr21:43888988
|
C | CA | 95 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-111-14959dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43888988 | |||||
| chr21:43889095
|
A | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0276 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-111-14862A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889095 | ||||||
| chr21:43889208
|
A | C | 46 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(43): Show | 47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-111-14749A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889208 | ||||||
| chr21:43889220
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0002g0224 | 3 | HG02083.hp1 HG02132.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-111-14737C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889220 | ||||||
| chr21:43889286
|
G | GT | 86 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-111-14656dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43889286 | |||||
| chr21:43889286
|
GT | G | 9 | a0001c0001t0001g0172a0001c0001t0001g0221a0001c0001t0006g0205others(6): Show | 9 | HG00323.hp2 HG01081.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-111-14656delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43889286 | |||||
| chr21:43889524
|
A | G | 1 | a0001c0001t0006g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-111-14433A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889524 | ||||||
| chr21:43889568
|
C | T | 2 | a0001c0001t0007g0192a0001c0001t0053g0321 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-111-14389C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889568 | ||||||
| chr21:43889615
|
G | T | 1 | a0001c0001t0002g0339 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-111-14342G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889615 | ||||||
| chr21:43889623
|
A | G | 2 | a0001c0003t0011g0260a0001c0003t0011g0261 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-111-14334A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889623 | ||||||
| chr21:43889717
|
C | T | 1 | a0001c0001t0038g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-111-14240C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889717 | ||||||
| chr21:43889776
|
A | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-111-14181A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889776 | ||||||
| chr21:43889961
|
GACATTTT others(22): Show |
G | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-111-13983_-111-13 others(35): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43889961 | |||||
| chr21:43890659
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0049g0320 | 2 | HG00423.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-111-13298C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43890659 | ||||||
| chr21:43890715
|
G | GT | 274 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-111-13230dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43890715 | |||||
| chr21:43890715
|
G | GTT | 14 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0338others(11): Show | 14 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.-111-13231_-111-13 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43890715 | |||||
| chr21:43890729
|
A | G | 5 | a0001c0001t0006g0205a0001c0001t0049g0320a0001c0001t0051g0207others(2): Show | 5 | HG01081.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-13228A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43890729 | ||||||
| chr21:43891079
|
C | T | 1 | a0001c0001t0004g0044 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-111-12878C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891079 | ||||||
| chr21:43891080
|
G | A | 6 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(3): Show | 6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-111-12877G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891080 | ||||||
| chr21:43891147
|
G | A | 46 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(43): Show | 47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-111-12810G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891147 | ||||||
| chr21:43891150
|
A | G | 284 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-111-12807A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891150 | ||||||
| chr21:43891415
|
C | T | 2 | a0001c0001t0002g0258a0001c0001t0004g0317 | 2 | HG02135.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-111-12542C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891415 | ||||||
| chr21:43891557
|
C | T | 1 | a0001c0001t0072g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-111-12400C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891557 | ||||||
| chr21:43891803
|
C | T | 5 | a0001c0001t0001g0210a0001c0001t0001g0223a0001c0001t0001g0255others(2): Show | 5 | HG00621.hp1 NA18968.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-12154C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891803 | ||||||
| chr21:43891874
|
T | G | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-12083T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891874 | ||||||
| chr21:43891919
|
C | A | 289 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-111-12038C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891919 | ||||||
| chr21:43891920
|
A | G | 5 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(2): Show | 5 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-12037A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891920 | ||||||
| chr21:43892135
|
C | T | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-111-11822C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892135 | ||||||
| chr21:43892168
|
G | A | 1 | a0001c0001t0003g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-111-11789G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892168 | ||||||
| chr21:43892199
|
C | T | 3 | a0001c0001t0006g0097a0001c0001t0010g0095a0001c0001t0010g0096 | 3 | HG00639.hp1 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-111-11758C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892199 | ||||||
| chr21:43892228
|
A | G | 1 | a0001c0001t0078g0316 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-111-11729A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892228 | ||||||
| chr21:43892239
|
G | A | 48 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(45): Show | 49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-11718G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892239 | ||||||
| chr21:43892307
|
C | CA | 6 | a0001c0001t0001g0225a0001c0001t0001g0232a0001c0001t0001g0283others(3): Show | 6 | HG01175.hp2 HG02080.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-11638dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43892307 | |||||
| chr21:43892307
|
CA | C | 42 | a0001c0001t0001g0200a0001c0001t0004g0029a0001c0001t0005g0082others(39): Show | 43 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.-111-11638delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43892307 | |||||
| chr21:43892318
|
AAG | A | 8 | a0001c0001t0036g0094a0001c0001t0037g0304a0001c0001t0038g0109others(5): Show | 8 | HG02559.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-11637_-111-11 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43892318 | |||||
| chr21:43892368
|
C | T | 1 | a0001c0001t0005g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-111-11589C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892368 | ||||||
| chr21:43892405
|
T | C | 46 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(43): Show | 47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-111-11552T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892405 | ||||||
| chr21:43892471
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-111-11486A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892471 | ||||||
| chr21:43892673
|
A | G | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-11284A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892673 | ||||||
| chr21:43892933
|
A | G | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-11024A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892933 | ||||||
| chr21:43893222
|
A | G | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-10735A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893222 | ||||||
| chr21:43893276
|
A | G | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-10681A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893276 | ||||||
| chr21:43893313
|
C | T | 2 | a0001c0001t0011g0021a0001c0001t0011g0204 | 2 | NA18955.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-111-10644C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893313 | ||||||
| chr21:43893425
|
A | G | 2 | a0001c0001t0008g0158a0001c0001t0008g0159 | 2 | HG03834.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-111-10532A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893425 | ||||||
| chr21:43893429
|
C | G | 48 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(45): Show | 49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-10528C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893429 | ||||||
| chr21:43893509
|
A | C | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-111-10448A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893509 | ||||||
| chr21:43893635
|
C | A | 2 | a0001c0001t0051g0207a0001c0001t0057g0208 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-111-10322C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893635 | ||||||
| chr21:43893670
|
A | G | 4 | a0001c0001t0006g0097a0001c0001t0010g0063a0001c0001t0010g0095others(1): Show | 4 | HG00639.hp1 HG02109.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-10287A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893670 | ||||||
| chr21:43893695
|
C | G | 1 | a0001c0001t0001g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-111-10262C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893695 | ||||||
| chr21:43893800
|
C | T | 2 | a0001c0001t0005g0322a0002c0006t0010g0112 | 2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-111-10157C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893800 | ||||||
| chr21:43893978
|
C | T | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-9979C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893978 | ||||||
| chr21:43894042
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-111-9915G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894042 | ||||||
| chr21:43894079
|
C | A | 1 | a0001c0001t0002g0332 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-111-9878C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894079 | ||||||
| chr21:43894079
|
C | T | 6 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(3): Show | 6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-111-9878C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894079 | ||||||
| chr21:43894166
|
T | C | 1 | a0001c0001t0019g0330 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-111-9791T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894166 | ||||||
| chr21:43894217
|
C | CT | 83 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-111-9724dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43894217 | |||||
| chr21:43894217
|
CT | C | 16 | a0001c0001t0001g0163a0001c0001t0001g0175a0001c0001t0001g0200others(13): Show | 16 | HG01081.hp1 HG01256.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-111-9724delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43894217 | |||||
| chr21:43894220
|
T | TC | 7 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0023others(4): Show | 7 | HG01167.hp2 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-111-9737_-111-973 others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894220 | ||||||
| chr21:43894221
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-111-9736T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894221 | ||||||
| chr21:43894222
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-111-9735T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894222 | ||||||
| chr21:43894395
|
A | AT | 47 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(44): Show | 48 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.-111-9550dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43894395 | |||||
| chr21:43894438
|
C | A | 1 | a0001c0001t0078g0316 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-111-9519C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894438 | ||||||
| chr21:43894554
|
G | A | 4 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-9403G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894554 | ||||||
| chr21:43894608
|
G | A | 82 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-111-9349G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894608 | ||||||
| chr21:43894653
|
C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-111-9304C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894653 | ||||||
| chr21:43894897
|
A | G | 48 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(45): Show | 49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-9060A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894897 | ||||||
| chr21:43895032
|
T | A | 3 | a0001c0001t0040g0007a0001c0001t0041g0091a0001c0001t0042g0092 | 3 | HG02572.hp1 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-111-8925T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895032 | ||||||
| chr21:43895111
|
A | T | 6 | a0001c0001t0003g0085a0001c0001t0008g0143a0001c0001t0018g0084others(3): Show | 6 | HG00323.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-8846A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895111 | ||||||
| chr21:43895115
|
T | A | 6 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0003g0181others(3): Show | 6 | HG01081.hp1 HG01891.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-8842T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895115 | ||||||
| chr21:43895161
|
G | A | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-111-8796G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895161 | ||||||
| chr21:43895264
|
C | T | 48 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(45): Show | 49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-8693C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895264 | ||||||
| chr21:43895351
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | NA18747.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-111-8606C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895351 | ||||||
| chr21:43895409
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-111-8548T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895409 | ||||||
| chr21:43895485
|
C | A | 1 | a0001c0001t0021g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-111-8472C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895485 | ||||||
| chr21:43895509
|
A | AT | 9 | a0001c0001t0012g0076a0001c0001t0012g0099a0001c0001t0012g0101others(6): Show | 9 | HG01109.hp1 HG02615.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-8427dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43895509 | |||||
| chr21:43895509
|
AT | A | 222 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-111-8427delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43895509 | |||||
| chr21:43895594
|
A | T | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-111-8363A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895594 | ||||||
| chr21:43895603
|
T | A | 9 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(6): Show | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-8354T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895603 | ||||||
| chr21:43895651
|
G | A | 8 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-8306G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895651 | ||||||
| chr21:43895789
|
C | G | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-8168C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895789 | ||||||
| chr21:43896035
|
C | T | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-7922C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896035 | ||||||
| chr21:43896183
|
G | C | 41 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(38): Show | 42 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-111-7774G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896183 | ||||||
| chr21:43896195
|
C | T | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-7762C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896195 | ||||||
| chr21:43896201
|
G | A | 2 | a0001c0001t0014g0198a0001c0001t0014g0234 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-111-7756G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896201 | ||||||
| chr21:43896204
|
G | A | 41 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(38): Show | 42 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-111-7753G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896204 | ||||||
| chr21:43896207
|
A | G | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-7750A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896207 | ||||||
| chr21:43896262
|
C | T | 1 | a0001c0001t0019g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-111-7695C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896262 | ||||||
| chr21:43896285
|
G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-7672G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896285 | ||||||
| chr21:43896430
|
T | C | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-7527T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896430 | ||||||
| chr21:43896580
|
G | A | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-7377G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896580 | ||||||
| chr21:43896697
|
A | G | 1 | a0001c0001t0040g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-111-7260A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896697 | ||||||
| chr21:43896734
|
A | AT | 4 | a0001c0001t0006g0194a0001c0001t0031g0195a0001c0001t0031g0196others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-7221dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43896734 | |||||
| chr21:43896943
|
G | GT | 47 | a0001c0001t0001g0058a0001c0001t0001g0151a0001c0001t0001g0152others(44): Show | 47 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.-111-6989dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43896943 | |||||
| chr21:43896943
|
GT | G | 91 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(88): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-111-6989delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43896943 | |||||
| chr21:43896943
|
GTT | G | 11 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(8): Show | 12 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-111-6990_-111-698 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43896943 | |||||
| chr21:43896950
|
T | G | 2 | a0001c0001t0019g0069a0001c0008t0071g0068 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-7007T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896950 | ||||||
| chr21:43896958
|
T | G | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-6999T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896958 | ||||||
| chr21:43896976
|
T | C | 1 | a0001c0001t0008g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-111-6981T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896976 | ||||||
| chr21:43897103
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-111-6854G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897103 | ||||||
| chr21:43897184
|
G | A | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6773G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897184 | ||||||
| chr21:43897282
|
A | T | 1 | a0001c0001t0004g0011 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-111-6675A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897282 | ||||||
| chr21:43897340
|
C | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-111-6617C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897340 | ||||||
| chr21:43897345
|
A | G | 86 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-111-6612A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897345 | ||||||
| chr21:43897456
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-111-6501C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897456 | ||||||
| chr21:43897484
|
A | G | 267 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.-111-6473A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897484 | ||||||
| chr21:43897530
|
C | CGCTCCTC others(104): Show |
39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6418_-111-641 others(115): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43897530 | |||||
| chr21:43897540
|
A | ATCCCAGA others(30): Show |
2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | NA18747.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-111-6410_-111-640 others(41): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43897540 | |||||
| chr21:43897540
|
A | C | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6417A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897540 | ||||||
| chr21:43897540
|
ATCCCAGA others(67): Show |
A | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-111-6345_-111-627 others(78): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43897540 | |||||
| chr21:43897567
|
C | G | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6390C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897567 | ||||||
| chr21:43897577
|
A | C | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6380A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897577 | ||||||
| chr21:43897585
|
C | G | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6372C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897585 | ||||||
| chr21:43897627
|
C | T | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6330C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897627 | ||||||
| chr21:43897631
|
C | T | 35 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0132others(32): Show | 36 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-111-6326C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897631 | ||||||
| chr21:43897640
|
GCGCTCCT others(67): Show |
G | 1 | a0001c0001t0006g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-111-6306_-111-623 others(78): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43897640 | |||||
| chr21:43897641
|
C | G | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6316C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897641 | ||||||
| chr21:43897649
|
A | C | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6308A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897649 | ||||||
| chr21:43897660
|
G | A | 40 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(37): Show | 41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-111-6297G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897660 | ||||||
| chr21:43897678
|
G | T | 4 | a0001c0001t0001g0253a0001c0001t0014g0198a0001c0001t0014g0234others(1): Show | 4 | HG01070.hp1 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-6279G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897678 | ||||||
| chr21:43897705
|
T | C | 46 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(43): Show | 47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-111-6252T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897705 | ||||||
| chr21:43898000
|
G | A | 1 | a0001c0001t0003g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-111-5957G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898000 | ||||||
| chr21:43898024
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0232a0001c0001t0001g0283 | 3 | HG02080.hp1 NA19002.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-111-5933A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898024 | ||||||
| chr21:43898056
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG01099.hp1 HG01123.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-111-5901G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898056 | ||||||
| chr21:43898125
|
A | G | 3 | a0001c0001t0019g0069a0001c0001t0049g0320a0001c0008t0071g0068 | 3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-5832A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898125 | ||||||
| chr21:43898157
|
T | C | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-5800T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898157 | ||||||
| chr21:43898176
|
A | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-111-5781A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898176 | ||||||
| chr21:43898454
|
C | T | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-111-5503C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898454 | ||||||
| chr21:43898486
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-111-5471C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898486 | ||||||
| chr21:43898491
|
G | A | 3 | a0001c0001t0004g0286a0001c0001t0004g0314a0001c0001t0021g0262 | 3 | HG00741.hp1 HG01192.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-111-5466G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898491 | ||||||
| chr21:43898620
|
A | G | 40 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(37): Show | 41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-111-5337A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898620 | ||||||
| chr21:43898742
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-111-5215A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898742 | ||||||
| chr21:43898860
|
C | T | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-111-5097C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898860 | ||||||
| chr21:43898885
|
G | GT | 98 | a0001c0001t0001g0113a0001c0001t0001g0150a0001c0001t0001g0168others(95): Show | 98 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-111-5061dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43898885 | |||||
| chr21:43898891
|
T | G | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-111-5066T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898891 | ||||||
| chr21:43899052
|
G | A | 1 | a0001c0001t0004g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-111-4905G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899052 | ||||||
| chr21:43899067
|
C | T | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-4890C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899067 | ||||||
| chr21:43899075
|
A | G | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-4882A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899075 | ||||||
| chr21:43899143
|
T | C | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-4814T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899143 | ||||||
| chr21:43899170
|
C | CTT | 289 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-111-4786_-111-478 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43899170 | |||||
| chr21:43899289
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-111-4668G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899289 | ||||||
| chr21:43899410
|
C | T | 5 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(2): Show | 5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-4547C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899410 | ||||||
| chr21:43899525
|
C | T | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-4432C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899525 | ||||||
| chr21:43899553
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0002g0267 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-111-4404C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899553 | ||||||
| chr21:43899615
|
G | A | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-111-4342G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899615 | ||||||
| chr21:43899625
|
G | A | 4 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-4332G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899625 | ||||||
| chr21:43899738
|
C | T | 132 | a0001c0001t0001g0113a0001c0001t0001g0142a0001c0001t0001g0164others(129): Show | 133 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-111-4219C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899738 | ||||||
| chr21:43899741
|
G | A | 9 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(6): Show | 9 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-4216G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899741 | ||||||
| chr21:43899772
|
G | C | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-4185G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899772 | ||||||
| chr21:43899904
|
A | AG | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-4051dupG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43899904 | |||||
| chr21:43900054
|
T | C | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-111-3903T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900054 | ||||||
| chr21:43900067
|
T | C | 1 | a0001c0009t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-111-3890T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900067 | ||||||
| chr21:43900295
|
C | G | 4 | a0001c0001t0006g0194a0001c0001t0031g0195a0001c0001t0031g0196others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-3662C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900295 | ||||||
| chr21:43900402
|
G | A | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-3555G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900402 | ||||||
| chr21:43900725
|
G | A | 5 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(2): Show | 5 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-3232G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900725 | ||||||
| chr21:43900776
|
G | A | 9 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(6): Show | 9 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-3181G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900776 | ||||||
| chr21:43900795
|
G | T | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-111-3162G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900795 | ||||||
| chr21:43900821
|
C | T | 3 | a0001c0001t0019g0069a0001c0001t0049g0320a0001c0008t0071g0068 | 3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-3136C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900821 | ||||||
| chr21:43900822
|
G | A | 1 | a0001c0001t0004g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-111-3135G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900822 | ||||||
| chr21:43900832
|
T | C | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-3125T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900832 | ||||||
| chr21:43901107
|
T | G | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-2850T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901107 | ||||||
| chr21:43901320
|
TA | T | 9 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0006g0194others(6): Show | 9 | HG00558.hp1 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-2618delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901320 | |||||
| chr21:43901320
|
TAA | T | 194 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.-111-2619_-111-261 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901320 | |||||
| chr21:43901320
|
TAAA | T | 45 | a0001c0001t0001g0017a0001c0001t0001g0142a0001c0001t0001g0164others(42): Show | 46 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-111-2620_-111-261 others(7): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901320 | |||||
| chr21:43901320
|
TAAAA | T | 37 | a0001c0001t0005g0086a0001c0001t0005g0088a0001c0001t0005g0089others(34): Show | 38 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.-111-2621_-111-261 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901320 | |||||
| chr21:43901442
|
A | ATG | 282 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.-111-2514_-111-251 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901442 | |||||
| chr21:43901485
|
T | TAAAAAAA others(310): Show |
3 | a0001c0001t0051g0207a0001c0001t0057g0208a0001c0001t0072g0209 | 3 | HG01081.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-111-2459_-111-245 others(321): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901485 | |||||
| chr21:43901485
|
T | TAAAAAAA others(311): Show |
1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-111-2459_-111-245 others(322): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901485 | |||||
| chr21:43901486
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-111-2471A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901486 | ||||||
| chr21:43901503
|
C | A | 1 | a0001c0001t0001g0235 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-111-2454C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901503 | ||||||
| chr21:43901656
|
C | T | 2 | a0001c0001t0003g0153a0001c0001t0007g0154 | 2 | NA18945.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-111-2301C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901656 | ||||||
| chr21:43901708
|
G | A | 13 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(10): Show | 13 | HG00558.hp2 HG00621.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.-111-2249G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901708 | ||||||
| chr21:43901716
|
A | G | 3 | a0001c0001t0011g0021a0001c0001t0011g0166a0001c0001t0011g0204 | 3 | HG02040.hp1 NA18955.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-111-2241A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901716 | ||||||
| chr21:43901790
|
A | G | 1 | a0001c0001t0014g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-111-2167A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901790 | ||||||
| chr21:43901867
|
A | G | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-2090A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901867 | ||||||
| chr21:43902507
|
C | G | 282 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.-111-1450C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902507 | ||||||
| chr21:43902601
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0175 | 2 | NA19056.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-111-1356T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902601 | ||||||
| chr21:43902702
|
C | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-111-1255C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902702 | ||||||
| chr21:43902703
|
G | A | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-1254G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902703 | ||||||
| chr21:43902705
|
C | T | 1 | a0001c0001t0006g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-111-1252C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902705 | ||||||
| chr21:43902764
|
C | T | 1 | a0001c0001t0009g0284 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-111-1193C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902764 | ||||||
| chr21:43902821
|
A | G | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-1136A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902821 | ||||||
| chr21:43902860
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-111-1097C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902860 | ||||||
| chr21:43902942
|
G | T | 1 | a0001c0001t0010g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-111-1015G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902942 | ||||||
| chr21:43902949
|
G | A | 1 | a0001c0001t0037g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-111-1008G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902949 | ||||||
| chr21:43902988
|
G | A | 40 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(37): Show | 41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-111-969G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902988 | ||||||
| chr21:43903013
|
A | T | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-944A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903013 | ||||||
| chr21:43903134
|
T | C | 3 | a0001c0001t0019g0069a0001c0001t0049g0320a0001c0008t0071g0068 | 3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-823T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903134 | ||||||
| chr21:43903158
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-111-799A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903158 | ||||||
| chr21:43903158
|
A | T | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-799A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903158 | ||||||
| chr21:43903213
|
C | T | 9 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(6): Show | 10 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-111-744C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903213 | ||||||
| chr21:43903298
|
G | A | 5 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(2): Show | 5 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-659G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903298 | ||||||
| chr21:43903318
|
A | G | 2 | a0001c0001t0008g0042a0001c0001t0008g0043 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-111-639A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903318 | ||||||
| chr21:43903442
|
C | T | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-515C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903442 | ||||||
| chr21:43903518
|
G | T | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-439G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903518 | ||||||
| chr21:43903529
|
C | T | 1 | a0001c0001t0019g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-111-428C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903529 | ||||||
| chr21:43903531
|
G | T | 34 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0132others(31): Show | 35 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-111-426G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903531 | ||||||
| chr21:43903585
|
G | A | 1 | a0001c0005t0001g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-111-372G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903585 | ||||||
| chr21:43903679
|
G | A | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-278G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903679 | ||||||
| chr21:43903690
|
C | T | 4 | a0001c0001t0024g0106a0001c0001t0024g0107a0001c0001t0034g0105others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-267C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903690 | ||||||
| chr21:43903765
|
T | C | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-192T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903765 | ||||||
| chr21:43903827
|
T | A | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-130T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903827 | ||||||
| chr21:43903835
|
C | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0166a0001c0001t0011g0204 | 3 | HG02040.hp1 NA18955.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-111-122C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903835 | ||||||
| chr21:43904065
|
A | AGT | 3 | a0001c0001t0015g0115a0001c0001t0051g0207a0001c0001t0063g0273 | 3 | HG02970.hp1 NA18985.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-49+83_-49+84dupGT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | |||||
| chr21:43904065
|
A | AGTGT | 8 | a0001c0001t0001g0150a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49+81_-49+84dupGT others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | |||||
| chr21:43904065
|
AGT | A | 166 | a0001c0001t0001g0113a0001c0001t0001g0142a0001c0001t0001g0145others(163): Show | 167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-49+83_-49+84delGT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | |||||
| chr21:43904065
|
AGTGT | A | 90 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.-49+81_-49+84delGT others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | |||||
| chr21:43904065
|
AGTGTGT | A | 6 | a0001c0001t0002g0224a0001c0001t0004g0340a0001c0001t0019g0069others(3): Show | 6 | HG02486.hp1 HG02559.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+79_-49+84delGT others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | |||||
| chr21:43904065
|
AGTGTGTG others(7): Show |
A | 2 | a0001c0001t0036g0094a0001c0001t0037g0304 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-49+71_-49+84delGT others(12): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | |||||
| chr21:43904065
|
AGTGTGTG others(9): Show |
A | 37 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(34): Show | 38 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.-49+69_-49+84delGT others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | |||||
| chr21:43904071
|
T | A | 1 | a0001c0001t0018g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-49+52T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904071 | ||||||
| chr21:43904126
|
C | T | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0276 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-49+107C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904126 | ||||||
| chr21:43904328
|
G | T | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-49+309G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904328 | ||||||
| chr21:43904375
|
C | T | 1 | a0001c0001t0021g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-49+356C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904375 | ||||||
| chr21:43904406
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-49+387C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904406 | ||||||
| chr21:43904483
|
G | A | 5 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(2): Show | 5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+464G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904483 | ||||||
| chr21:43904687
|
G | A | 3 | a0001c0001t0040g0007a0001c0001t0041g0091a0001c0001t0042g0092 | 3 | HG02572.hp1 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-49+668G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904687 | ||||||
| chr21:43904773
|
C | G | 2 | a0001c0001t0028g0242a0001c0001t0063g0273 | 2 | NA18962.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-49+754C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904773 | ||||||
| chr21:43904800
|
C | T | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-49+781C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904800 | ||||||
| chr21:43904804
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0163 | 2 | HG01256.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-49+785C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904804 | ||||||
| chr21:43904851
|
G | C | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-49+832G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904851 | ||||||
| chr21:43904936
|
C | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(14): Show | 18 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-49+917C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904936 | ||||||
| chr21:43905147
|
T | A | 1 | a0001c0001t0002g0183 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-49+1128T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905147 | ||||||
| chr21:43905148
|
A | T | 273 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(270): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.-49+1129A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905148 | ||||||
| chr21:43905155
|
A | ATATT | 16 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0151others(13): Show | 16 | HG00423.hp2 HG00733.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49+1186_-49+1189d others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | |||||
| chr21:43905155
|
ATATT | A | 136 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0028others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-49+1186_-49+1189d others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | |||||
| chr21:43905155
|
ATATTTAT others(1): Show |
A | 42 | a0001c0001t0001g0054a0001c0001t0001g0210a0001c0001t0001g0223others(39): Show | 42 | HG00597.hp1 HG00621.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.-49+1182_-49+1189d others(10): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | |||||
| chr21:43905155
|
ATATTTAT others(5): Show |
A | 61 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0001g0310others(58): Show | 62 | HG00544.hp2 HG00738.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.-49+1178_-49+1189d others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | |||||
| chr21:43905155
|
ATATTTAT others(9): Show |
A | 5 | a0001c0001t0003g0085a0001c0001t0003g0127a0001c0001t0018g0084others(2): Show | 6 | HG01069.hp2 HG01071.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49+1174_-49+1189d others(18): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | |||||
| chr21:43905155
|
ATATTTAT others(13): Show |
A | 6 | a0001c0001t0010g0095a0001c0001t0010g0096a0001c0001t0012g0070others(3): Show | 6 | HG00639.hp1 NA18522.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+1170_-49+1189d others(22): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | |||||
| chr21:43905155
|
ATATTTAT others(17): Show |
A | 1 | a0001c0001t0003g0160 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-49+1166_-49+1189d others(26): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | |||||
| chr21:43905259
|
G | A | 5 | a0001c0001t0036g0094a0001c0001t0037g0304a0001c0001t0038g0109others(2): Show | 5 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+1240G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905259 | ||||||
| chr21:43905264
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-49+1245A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905264 | ||||||
| chr21:43905288
|
C | T | 1 | a0001c0001t0037g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-49+1269C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905288 | ||||||
| chr21:43905484
|
G | A | 1 | a0001c0001t0003g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-49+1465G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905484 | ||||||
| chr21:43905487
|
C | G | 39 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-49+1468C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905487 | ||||||
| chr21:43905490
|
G | A | 1 | a0001c0001t0073g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-49+1471G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905490 | ||||||
| chr21:43905496
|
C | T | 2 | a0001c0001t0016g0071a0001c0001t0016g0072 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49+1477C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905496 | ||||||
| chr21:43905577
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-49+1558C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905577 | ||||||
| chr21:43906035
|
G | T | 131 | a0001c0001t0001g0113a0001c0001t0001g0142a0001c0001t0001g0164others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-49+2016G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906035 | ||||||
| chr21:43906080
|
G | T | 1 | a0001c0001t0008g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-49+2061G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906080 | ||||||
| chr21:43906088
|
G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-49+2069G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906088 | ||||||
| chr21:43906135
|
G | A | 1 | a0001c0001t0002g0307 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49+2116G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906135 | ||||||
| chr21:43906223
|
C | G | 2 | a0001c0001t0015g0115a0001c0002t0018g0114 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-49+2204C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906223 | ||||||
| chr21:43906238
|
C | T | 8 | a0001c0001t0012g0076a0001c0001t0012g0099a0001c0001t0012g0101others(5): Show | 8 | HG01109.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49+2219C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906238 | ||||||
| chr21:43906332
|
C | G | 1 | a0001c0001t0001g0334 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-49+2313C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906332 | ||||||
| chr21:43906334
|
G | T | 1 | a0001c0001t0038g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-49+2315G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906334 | ||||||
| chr21:43906517
|
T | C | 40 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(37): Show | 41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+2498T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906517 | ||||||
| chr21:43906571
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-49+2552G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906571 | ||||||
| chr21:43906577
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-49+2558A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906577 | ||||||
| chr21:43906583
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-49+2564C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906583 | ||||||
| chr21:43906720
|
G | A | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49+2701G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906720 | ||||||
| chr21:43906784
|
C | A | 40 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(37): Show | 41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+2765C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906784 | ||||||
| chr21:43906879
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-49+2860C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906879 | ||||||
| chr21:43907029
|
C | CT | 15 | a0001c0001t0001g0200a0001c0001t0001g0222a0001c0001t0001g0243others(12): Show | 15 | HG00544.hp2 HG00639.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49+3030dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43907029 | |||||
| chr21:43907029
|
CT | C | 44 | a0001c0001t0001g0164a0001c0001t0002g0015a0001c0001t0005g0082others(41): Show | 45 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.-49+3030delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43907029 | |||||
| chr21:43907058
|
G | T | 83 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-49+3039G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907058 | ||||||
| chr21:43907153
|
C | T | 1 | a0001c0001t0023g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-49+3134C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907153 | ||||||
| chr21:43907154
|
C | G | 40 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(37): Show | 41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+3135C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907154 | ||||||
| chr21:43907196
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-49+3177C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907196 | ||||||
| chr21:43907228
|
C | G | 36 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0132others(33): Show | 37 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(34): Show |
intron_variant | MODIFIER | c.-49+3209C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907228 | ||||||
| chr21:43907445
|
C | T | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-49+3426C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907445 | ||||||
| chr21:43907573
|
T | C | 1 | a0001c0001t0003g0127 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-49+3554T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907573 | ||||||
| chr21:43907606
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-49+3587A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907606 | ||||||
| chr21:43907695
|
C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+3676C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907695 | ||||||
| chr21:43907713
|
T | C | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+3694T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907713 | ||||||
| chr21:43907731
|
C | CA | 15 | a0001c0001t0001g0034a0001c0001t0001g0180a0001c0001t0001g0255others(12): Show | 15 | HG00733.hp1 HG01433.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49+3719dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43907731 | |||||
| chr21:43907869
|
G | A | 85 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-49+3850G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907869 | ||||||
| chr21:43907889
|
C | T | 40 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(37): Show | 41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+3870C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907889 | ||||||
| chr21:43907967
|
C | T | 132 | a0001c0001t0001g0113a0001c0001t0001g0142a0001c0001t0001g0164others(129): Show | 133 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-49+3948C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907967 | ||||||
| chr21:43908286
|
G | A | 4 | a0001c0001t0006g0194a0001c0001t0031g0195a0001c0001t0031g0196others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+4267G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908286 | ||||||
| chr21:43908308
|
C | A | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-49+4289C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908308 | ||||||
| chr21:43908319
|
G | A | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-49+4300G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908319 | ||||||
| chr21:43908405
|
C | T | 1 | a0001c0001t0002g0333 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-49+4386C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908405 | ||||||
| chr21:43908557
|
G | A | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+4538G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908557 | ||||||
| chr21:43908594
|
A | C | 2 | a0001c0001t0030g0073a0001c0001t0030g0331 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-49+4575A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908594 | ||||||
| chr21:43908984
|
G | A | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+4965G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908984 | ||||||
| chr21:43909121
|
C | G | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+5102C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909121 | ||||||
| chr21:43909208
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-49+5189C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909208 | ||||||
| chr21:43909244
|
C | T | 1 | a0001c0001t0010g0095 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-49+5225C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909244 | ||||||
| chr21:43909291
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-49+5272C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909291 | ||||||
| chr21:43909292
|
AT | A | 230 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.-49+5294delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43909292 | |||||
| chr21:43909292
|
ATTTT | A | 42 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(39): Show | 43 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.-49+5291_-49+5294d others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43909292 | |||||
| chr21:43909330
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0046 | 2 | HG01168.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-49+5311C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909330 | ||||||
| chr21:43909420
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0023others(3): Show | 6 | HG01167.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+5401C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909420 | ||||||
| chr21:43909440
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0237a0001c0001t0001g0268others(1): Show | 4 | HG02015.hp2 HG02080.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+5421C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909440 | ||||||
| chr21:43909535
|
A | C | 40 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(37): Show | 41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+5516A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909535 | ||||||
| chr21:43909583
|
A | G | 2 | a0001c0001t0019g0323a0001c0001t0019g0330 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-49+5564A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909583 | ||||||
| chr21:43909723
|
G | A | 1 | a0001c0001t0002g0307 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49+5704G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909723 | ||||||
| chr21:43909870
|
A | C | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+5851A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909870 | ||||||
| chr21:43909982
|
G | A | 5 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(2): Show | 5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+5963G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909982 | ||||||
| chr21:43910002
|
C | T | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-49+5983C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910002 | ||||||
| chr21:43910218
|
C | T | 1 | a0001c0001t0079g0228 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-49+6199C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910218 | ||||||
| chr21:43910353
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-49+6334C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910353 | ||||||
| chr21:43910640
|
C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+6621C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910640 | ||||||
| chr21:43910736
|
A | G | 40 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(37): Show | 41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+6717A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910736 | ||||||
| chr21:43910932
|
A | G | 1 | a0001c0001t0009g0230 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-49+6913A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910932 | ||||||
| chr21:43910936
|
C | T | 1 | a0001c0001t0012g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-49+6917C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910936 | ||||||
| chr21:43910960
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-49+6941A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910960 | ||||||
| chr21:43911020
|
G | A | 1 | a0001c0001t0014g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-49+7001G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911020 | ||||||
| chr21:43911057
|
C | G | 1 | a0001c0001t0008g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-49+7038C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911057 | ||||||
| chr21:43911284
|
T | C | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | HG01167.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-49+7265T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911284 | ||||||
| chr21:43911323
|
A | G | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-49+7304A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911323 | ||||||
| chr21:43911332
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-49+7313C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911332 | ||||||
| chr21:43911343
|
T | TAAAGACT others(3179): Show |
1 | a0001c0001t0001g0287 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-49+7340_-49+7341i others(3188): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43911343 | |||||
| chr21:43911343
|
T | TAAAGACT others(3197): Show |
1 | a0001c0001t0001g0268 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-49+7340_-49+7341i others(3206): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43911343 | |||||
| chr21:43911343
|
T | TAAAGACT others(3199): Show |
1 | a0001c0001t0001g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-49+7340_-49+7341i others(3208): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43911343 | |||||
| chr21:43911343
|
T | TAAAGACT others(3182): Show |
1 | a0001c0001t0001g0237 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-49+7340_-49+7341i others(3191): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43911343 | |||||
| chr21:43911417
|
G | C | 8 | a0001c0001t0012g0076a0001c0001t0012g0099a0001c0001t0012g0101others(5): Show | 8 | HG01109.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49+7398G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911417 | ||||||
| chr21:43911773
|
T | A | 1 | a0001c0001t0004g0281 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-49+7754T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911773 | ||||||
| chr21:43911825
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-49+7806G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911825 | ||||||
| chr21:43912300
|
G | A | 2 | a0001c0001t0016g0071a0001c0001t0016g0072 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49+8281G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912300 | ||||||
| chr21:43912312
|
C | T | 1 | a0001c0001t0004g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-49+8293C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912312 | ||||||
| chr21:43912313
|
G | A | 9 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0020g0064others(6): Show | 9 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+8294G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912313 | ||||||
| chr21:43912345
|
G | A | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49+8326G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912345 | ||||||
| chr21:43912896
|
C | T | 2 | a0001c0001t0005g0322a0002c0006t0010g0112 | 2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49+8877C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912896 | ||||||
| chr21:43912897
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-49+8878G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912897 | ||||||
| chr21:43913164
|
CAG | C | 6 | a0001c0001t0001g0233a0001c0001t0015g0115a0001c0001t0015g0116others(3): Show | 6 | HG01261.hp2 HG01496.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+9147_-49+9148d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43913164 | |||||
| chr21:43913572
|
C | T | 3 | a0001c0001t0019g0069a0001c0001t0049g0320a0001c0008t0071g0068 | 3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-49+9553C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43913572 | ||||||
| chr21:43913984
|
A | G | 83 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-49+9965A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43913984 | ||||||
| chr21:43914056
|
G | A | 83 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-49+10037G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43914056 | ||||||
| chr21:43914074
|
C | T | 2 | a0001c0001t0006g0205a0001c0001t0072g0209 | 2 | HG01081.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-49+10055C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43914074 | ||||||
| chr21:43914118
|
T | A | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+10099T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43914118 | ||||||
| chr21:43914227
|
C | T | 1 | a0001c0001t0008g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-49+10208C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43914227 | ||||||
| chr21:43914346
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-49+10327T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43914346 | ||||||
| chr21:43914533
|
T | TTTTTG | 4 | a0001c0001t0003g0085a0001c0001t0008g0039a0001c0001t0018g0084others(1): Show | 4 | HG02647.hp1 HG02683.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+10544_-49+1054 others(9): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43914533 | |||||
| chr21:43914533
|
TTTTTGTT others(3): Show |
T | 4 | a0001c0001t0001g0197a0001c0001t0001g0231a0001c0001t0001g0265others(1): Show | 4 | NA18973.hp2 NA18975.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+10539_-49+1054 others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43914533 | |||||
| chr21:43914533
|
TTTTTGTT others(8): Show |
T | 9 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+10534_-49+1054 others(19): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43914533 | |||||
| chr21:43915294
|
C | T | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49+11275C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43915294 | ||||||
| chr21:43915405
|
C | CT | 140 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0031others(137): Show | 141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-49+11412dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43915405 | |||||
| chr21:43915405
|
C | CTT | 39 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0201others(36): Show | 40 | HG00099.hp2 HG00423.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-49+11411_-49+1141 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43915405 | |||||
| chr21:43915405
|
C | CTTT | 9 | a0001c0001t0001g0058a0001c0001t0005g0089a0001c0001t0005g0322others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+11410_-49+1141 others(7): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43915405 | |||||
| chr21:43915405
|
CT | C | 6 | a0001c0001t0006g0205a0001c0001t0007g0192a0001c0001t0051g0207others(3): Show | 6 | HG01081.hp1 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+11412delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43915405 | |||||
| chr21:43915415
|
T | C | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49+11396T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43915415 | ||||||
| chr21:43915765
|
A | T | 1 | a0001c0001t0040g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-49+11746A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43915765 | ||||||
| chr21:43915802
|
A | T | 2 | a0001c0001t0002g0023a0001c0001t0003g0236 | 2 | HG00597.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-49+11783A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43915802 | ||||||
| chr21:43916192
|
A | G | 4 | a0001c0001t0001g0197a0001c0001t0001g0231a0001c0001t0001g0265others(1): Show | 4 | NA18973.hp2 NA18975.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+12173A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916192 | ||||||
| chr21:43916285
|
C | T | 1 | a0001c0002t0018g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49+12266C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916285 | ||||||
| chr21:43916295
|
T | G | 1 | a0001c0001t0003g0130 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-49+12276T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916295 | ||||||
| chr21:43916469
|
A | G | 5 | a0001c0001t0003g0002a0001c0001t0003g0139a0001c0001t0003g0140others(2): Show | 6 | HG02258.hp2 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49+12450A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916469 | ||||||
| chr21:43916471
|
C | T | 4 | a0001c0001t0036g0094a0001c0001t0037g0304a0001c0001t0038g0109others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+12452C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916471 | ||||||
| chr21:43916530
|
A | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0060 | 2 | NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-49+12511A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916530 | ||||||
| chr21:43916543
|
C | CT | 69 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0142others(66): Show | 70 | HG00544.hp2 HG00639.hp1 HG01074.hp2 others(67): Show |
intron_variant | MODIFIER | c.-49+12538dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43916543 | |||||
| chr21:43916543
|
C | CTT | 6 | a0001c0001t0005g0086a0001c0001t0005g0088a0001c0001t0005g0089others(3): Show | 6 | HG00738.hp1 HG02602.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+12537_-49+1253 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43916543 | |||||
| chr21:43916543
|
C | T | 2 | a0001c0001t0016g0071a0001c0001t0016g0072 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49+12524C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916543 | ||||||
| chr21:43916543
|
CT | C | 7 | a0001c0001t0001g0235a0001c0001t0003g0085a0001c0001t0018g0084others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49+12538delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43916543 | |||||
| chr21:43916740
|
C | G | 4 | a0001c0001t0006g0194a0001c0001t0031g0195a0001c0001t0031g0196others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+12721C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916740 | ||||||
| chr21:43916893
|
C | T | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-49+12874C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916893 | ||||||
| chr21:43916928
|
C | T | 3 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208 | 3 | HG01891.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-49+12909C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916928 | ||||||
| chr21:43917009
|
C | T | 6 | a0001c0001t0001g0210a0001c0001t0001g0223a0001c0001t0001g0255others(3): Show | 6 | HG00621.hp1 HG02922.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49+12990C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917009 | ||||||
| chr21:43917010
|
G | A | 4 | a0001c0001t0007g0326a0001c0001t0007g0327a0001c0001t0007g0328others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+12991G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917010 | ||||||
| chr21:43917111
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-49+13092C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917111 | ||||||
| chr21:43917178
|
G | A | 43 | a0001c0001t0003g0085a0001c0001t0005g0082a0001c0001t0005g0086others(40): Show | 43 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.-49+13159G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917178 | ||||||
| chr21:43917191
|
G | A | 1 | a0001c0001t0078g0316 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-49+13172G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917191 | ||||||
| chr21:43917215
|
G | T | 47 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0296others(44): Show | 48 | HG00544.hp2 HG01257.hp1 HG01258.hp2 others(45): Show |
intron_variant | MODIFIER | c.-49+13196G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917215 | ||||||
| chr21:43917240
|
C | G | 1 | a0001c0001t0003g0130 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-49+13221C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917240 | ||||||
| chr21:43917271
|
G | A | 85 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-49+13252G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917271 | ||||||
| chr21:43917564
|
A | G | 80 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-49+13545A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917564 | ||||||
| chr21:43917666
|
G | A | 1 | a0001c0001t0050g0024 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-49+13647G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917666 | ||||||
| chr21:43917704
|
C | T | 38 | a0001c0001t0001g0142a0001c0001t0001g0155a0001c0001t0001g0156others(35): Show | 39 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.-49+13685C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917704 | ||||||
| chr21:43917787
|
ATTGTGGG others(16): Show |
A | 12 | a0001c0001t0010g0063a0001c0001t0010g0095a0001c0001t0010g0096others(9): Show | 12 | HG00639.hp1 HG01109.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-49+13777_-49+1379 others(27): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917787 | |||||
| chr21:43917796
|
ATTGTGGG others(16): Show |
A | 17 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(14): Show | 18 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-49+13792_-49+1381 others(27): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917796 | |||||
| chr21:43917804
|
G | GGTTGTGG others(134): Show |
2 | a0001c0001t0005g0322a0002c0006t0010g0112 | 2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49+13791_-49+1379 others(145): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917804 | |||||
| chr21:43917813
|
G | A | 2 | a0001c0001t0005g0322a0002c0006t0010g0112 | 2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49+13794G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917813 | ||||||
| chr21:43917814
|
T | C | 83 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-49+13795T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917814 | ||||||
| chr21:43917814
|
T | TGGGTGTT others(166): Show |
1 | a0001c0001t0001g0285 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-49+13823_-49+1382 others(177): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917814 | |||||
| chr21:43917834
|
GGTGTT | G | 116 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(113): Show | 116 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-49+13824_-49+1382 others(9): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917834 | |||||
| chr21:43917868
|
T | TGTTGTGG others(11): Show |
1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-49+13855_-49+1387 others(22): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917868 | |||||
| chr21:43917893
|
G | T | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-49+13874G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917893 | ||||||
| chr21:43917909
|
TGGGTGTT others(56): Show |
T | 4 | a0001c0001t0024g0106a0001c0001t0024g0107a0001c0001t0034g0105others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+13900_-49+1396 others(67): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917909 | |||||
| chr21:43917913
|
T | TGTTGTAG others(29): Show |
6 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0023others(3): Show | 6 | HG01167.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+13917_-49+1395 others(40): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917913 | |||||
| chr21:43917913
|
TGTTGTAG others(29): Show |
T | 6 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0003g0181others(3): Show | 6 | HG00639.hp2 HG01243.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+13917_-49+1395 others(40): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917913 | |||||
| chr21:43917934
|
TGTG | T | 129 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(126): Show | 130 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-49+13917_-49+1391 others(7): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917934 | |||||
| chr21:43917940
|
T | G | 133 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(130): Show | 134 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-49+13921T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917940 | ||||||
| chr21:43917940
|
T | TGTTGTGG others(62): Show |
1 | a0001c0001t0004g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-49+13935_-49+1393 others(73): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917940 | |||||
| chr21:43917976
|
TGTTGTGT others(16): Show |
T | 1 | a0001c0001t0015g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-49+13964_-49+1398 others(27): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917976 | |||||
| chr21:43917985
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-49+13966A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917985 | ||||||
| chr21:43918046
|
TG | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-49+14032delG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43918046 | |||||
| chr21:43918059
|
T | G | 150 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0200others(147): Show | 151 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.-49+14040T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918059 | ||||||
| chr21:43918065
|
GGTTGTGG others(2): Show |
G | 5 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(2): Show | 5 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+14071_-49+1407 others(13): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43918065 | |||||
| chr21:43918101
|
G | A | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+14082G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918101 | ||||||
| chr21:43918129
|
G | T | 1 | a0001c0001t0019g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-49+14110G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918129 | ||||||
| chr21:43918161
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0028g0018 | 2 | HG01346.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-49+14142G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918161 | ||||||
| chr21:43918203
|
G | GGTTGTGG others(20): Show |
83 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-49+14198_-49+1422 others(31): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43918203 | |||||
| chr21:43918318
|
T | C | 3 | a0001c0001t0002g0132a0001c0001t0002g0171a0001c0001t0003g0167 | 3 | NA19005.hp2 NA19064.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-49+14299T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918318 | ||||||
| chr21:43918346
|
T | C | 5 | a0001c0001t0036g0094a0001c0001t0037g0304a0001c0001t0038g0109others(2): Show | 5 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+14327T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918346 | ||||||
| chr21:43918390
|
C | T | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+14371C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918390 | ||||||
| chr21:43918391
|
G | A | 81 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-49+14372G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918391 | ||||||
| chr21:43918588
|
CT | C | 221 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-49+14585delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43918588 | |||||
| chr21:43918727
|
C | T | 20 | a0001c0001t0002g0296a0001c0001t0003g0080a0001c0001t0003g0119others(17): Show | 20 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-49+14708C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918727 | ||||||
| chr21:43918807
|
C | T | 1 | a0001c0001t0027g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-49+14788C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918807 | ||||||
| chr21:43919056
|
C | G | 1 | a0001c0001t0003g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-49+15037C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919056 | ||||||
| chr21:43919140
|
A | G | 1 | a0001c0001t0004g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-49+15121A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919140 | ||||||
| chr21:43919216
|
C | A | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-49+15197C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919216 | ||||||
| chr21:43919273
|
TG | T | 339 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(336): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-49+15256delG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43919273 | |||||
| chr21:43919407
|
G | A | 5 | a0001c0001t0003g0085a0001c0001t0003g0160a0001c0001t0018g0084others(2): Show | 5 | HG02055.hp1 HG02083.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+15388G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919407 | ||||||
| chr21:43919441
|
C | T | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-49+15422C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919441 | ||||||
| chr21:43919493
|
G | A | 1 | a0001c0001t0029g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-49+15474G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919493 | ||||||
| chr21:43919502
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-49+15483C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919502 | ||||||
| chr21:43919521
|
G | A | 32 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0296others(29): Show | 33 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-49+15502G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919521 | ||||||
| chr21:43919773
|
G | C | 5 | a0001c0001t0006g0205a0001c0001t0007g0192a0001c0001t0051g0207others(2): Show | 5 | HG01081.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+15754G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919773 | ||||||
| chr21:43920160
|
C | A | 25 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(22): Show | 25 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.-49+16141C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920160 | ||||||
| chr21:43920218
|
T | A | 1 | a0001c0001t0006g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-49+16199T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920218 | ||||||
| chr21:43920218
|
T | TGTGA | 234 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-49+16202_-49+1620 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43920218 | |||||
| chr21:43920219
|
G | GTGAA | 4 | a0001c0001t0017g0098a0001c0001t0040g0007a0001c0001t0041g0091others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+16202_-49+1620 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43920219 | |||||
| chr21:43920268
|
G | A | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+16249G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920268 | ||||||
| chr21:43920272
|
A | G | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-49+16253A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920272 | ||||||
| chr21:43920296
|
G | A | 239 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.-49+16277G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920296 | ||||||
| chr21:43920333
|
C | T | 1 | a0001c0001t0010g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-49+16314C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920333 | ||||||
| chr21:43920351
|
G | A | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-49+16332G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920351 | ||||||
| chr21:43920515
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-49+16496C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920515 | ||||||
| chr21:43920751
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-49+16732T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920751 | ||||||
| chr21:43920945
|
C | G | 1 | a0001c0001t0072g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-49+16926C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920945 | ||||||
| chr21:43921193
|
G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-49+17174G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921193 | ||||||
| chr21:43921305
|
C | T | 5 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(2): Show | 5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+17286C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921305 | ||||||
| chr21:43921325
|
T | G | 1 | a0001c0001t0007g0154 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-49+17306T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921325 | ||||||
| chr21:43921342
|
A | G | 1 | a0001c0001t0015g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-49+17323A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921342 | ||||||
| chr21:43921395
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0002g0267 | 2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-49+17376G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921395 | ||||||
| chr21:43921512
|
G | A | 2 | a0001c0001t0005g0082a0001c0001t0035g0303 | 2 | HG01074.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-49+17493G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921512 | ||||||
| chr21:43921579
|
T | C | 5 | a0001c0001t0001g0253a0001c0001t0014g0198a0001c0001t0014g0234others(2): Show | 5 | HG01070.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+17560T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921579 | ||||||
| chr21:43921701
|
T | A | 2 | a0001c0001t0008g0158a0001c0001t0008g0159 | 2 | HG03834.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-49+17682T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921701 | ||||||
| chr21:43921730
|
G | A | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+17711G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921730 | ||||||
| chr21:43921802
|
T | G | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+17783T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921802 | ||||||
| chr21:43921851
|
C | G | 141 | a0001c0001t0001g0054a0001c0001t0001g0113a0001c0001t0001g0197others(138): Show | 142 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-49+17832C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921851 | ||||||
| chr21:43921888
|
G | C | 4 | a0001c0001t0001g0300a0001c0001t0001g0334a0001c0001t0004g0012others(1): Show | 4 | HG00597.hp1 HG02074.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+17869G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921888 | ||||||
| chr21:43921910
|
A | G | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+17891A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921910 | ||||||
| chr21:43921965
|
G | A | 239 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.-49+17946G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921965 | ||||||
| chr21:43921973
|
G | T | 225 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.-49+17954G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921973 | ||||||
| chr21:43922040
|
T | C | 239 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.-49+18021T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922040 | ||||||
| chr21:43922323
|
C | T | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+18304C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922323 | ||||||
| chr21:43922471
|
C | G | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+18452C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922471 | ||||||
| chr21:43922650
|
T | C | 4 | a0001c0001t0006g0194a0001c0001t0031g0195a0001c0001t0031g0196others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+18631T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922650 | ||||||
| chr21:43922697
|
C | A | 2 | a0001c0001t0008g0042a0001c0001t0008g0043 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-49+18678C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922697 | ||||||
| chr21:43922724
|
T | A | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-49+18705T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922724 | ||||||
| chr21:43922761
|
G | A | 3 | a0001c0001t0002g0132a0001c0001t0002g0171a0001c0001t0003g0167 | 3 | NA19005.hp2 NA19064.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-49+18742G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922761 | ||||||
| chr21:43922778
|
C | G | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-49+18759C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922778 | ||||||
| chr21:43922847
|
C | T | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+18828C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922847 | ||||||
| chr21:43922948
|
C | T | 1 | a0001c0001t0002g0339 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-49+18929C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922948 | ||||||
| chr21:43922996
|
C | G | 5 | a0001c0001t0001g0300a0001c0001t0001g0334a0001c0001t0004g0012others(2): Show | 5 | HG00597.hp1 HG02015.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+18977C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922996 | ||||||
| chr21:43923140
|
G | A | 1 | a0001c0001t0047g0025 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-49+19121G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43923140 | ||||||
| chr21:43923433
|
C | T | 1 | a0001c0001t0014g0266 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-49+19414C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43923433 | ||||||
| chr21:43923479
|
G | A | 3 | a0001c0001t0001g0163a0001c0001t0016g0071a0001c0001t0016g0072 | 3 | HG01256.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49+19460G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43923479 | ||||||
| chr21:43923506
|
C | T | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-49+19487C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43923506 | ||||||
| chr21:43923925
|
A | G | 1 | a0001c0001t0009g0229 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-49+19906A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43923925 | ||||||
| chr21:43924155
|
A | T | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+20136A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924155 | ||||||
| chr21:43924170
|
C | T | 1 | a0001c0001t0017g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-49+20151C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924170 | ||||||
| chr21:43924190
|
AT | A | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0028others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-49+20187delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43924190 | |||||
| chr21:43924253
|
C | T | 47 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(44): Show | 48 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.-49+20234C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924253 | ||||||
| chr21:43924319
|
C | T | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+20300C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924319 | ||||||
| chr21:43924326
|
G | A | 146 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(143): Show | 147 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.-49+20307G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924326 | ||||||
| chr21:43924493
|
G | A | 4 | a0001c0001t0024g0106a0001c0001t0024g0107a0001c0001t0034g0105others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+20474G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924493 | ||||||
| chr21:43924503
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-49+20484G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924503 | ||||||
| chr21:43924535
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-49+20516G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924535 | ||||||
| chr21:43924605
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-49+20586G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924605 | ||||||
| chr21:43924677
|
G | A | 2 | a0001c0001t0014g0198a0001c0001t0014g0234 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-49+20658G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924677 | ||||||
| chr21:43924918
|
C | T | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+20899C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924918 | ||||||
| chr21:43925147
|
CT | C | 6 | a0001c0001t0017g0077a0001c0001t0017g0100a0001c0001t0036g0094others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+21129delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925147 | ||||||
| chr21:43925234
|
C | T | 3 | a0001c0001t0031g0195a0001c0001t0031g0196a0001c0001t0062g0313 | 3 | HG01257.hp1 HG01258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-49+21215C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925234 | ||||||
| chr21:43925241
|
C | T | 1 | a0001c0001t0027g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-49+21222C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925241 | ||||||
| chr21:43925242
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-49+21223G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925242 | ||||||
| chr21:43925275
|
G | A | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-49+21256G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925275 | ||||||
| chr21:43925300
|
C | T | 50 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0238others(47): Show | 51 | HG00544.hp2 HG01081.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.-49+21281C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925300 | ||||||
| chr21:43925439
|
G | C | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+21420G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925439 | ||||||
| chr21:43925582
|
A | G | 5 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(2): Show | 5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+21563A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925582 | ||||||
| chr21:43925585
|
C | T | 9 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(6): Show | 10 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-49+21566C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925585 | ||||||
| chr21:43925821
|
G | C | 1 | a0001c0001t0042g0092 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-49+21802G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925821 | ||||||
| chr21:43925835
|
T | C | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+21816T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925835 | ||||||
| chr21:43925861
|
A | G | 1 | a0001c0001t0005g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-49+21842A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925861 | ||||||
| chr21:43926373
|
C | T | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-49+22354C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926373 | ||||||
| chr21:43926383
|
C | T | 144 | a0001c0001t0001g0054a0001c0001t0001g0113a0001c0001t0001g0197others(141): Show | 145 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.-49+22364C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926383 | ||||||
| chr21:43926431
|
G | A | 2 | a0001c0001t0002g0078a0001c0001t0018g0081 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-49+22412G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926431 | ||||||
| chr21:43926549
|
G | A | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49+22530G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926549 | ||||||
| chr21:43926636
|
C | CT | 22 | a0001c0001t0001g0148a0001c0001t0001g0165a0001c0001t0001g0179others(19): Show | 22 | HG00140.hp1 HG00408.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-49+22646dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | |||||
| chr21:43926636
|
CT | C | 18 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0183others(15): Show | 19 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.-49+22646delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | |||||
| chr21:43926636
|
CTTTTT | C | 15 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 15 | HG00099.hp1 HG00741.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.-49+22642_-49+2264 others(9): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | |||||
| chr21:43926636
|
CTTTTTT | C | 110 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(107): Show | 111 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.-49+22641_-49+2264 others(10): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | |||||
| chr21:43926636
|
CTTTTTTT | C | 99 | a0001c0001t0001g0054a0001c0001t0001g0197a0001c0001t0001g0200others(96): Show | 99 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-49+22640_-49+2264 others(11): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | |||||
| chr21:43926636
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0006g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-49+22636_-49+2264 others(15): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | |||||
| chr21:43926636
|
CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0019g0323a0001c0001t0019g0330a0001c0001t0032g0324others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+22635_-49+2264 others(16): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | |||||
| chr21:43926636
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0006g0205a0001c0001t0072g0209 | 2 | HG01081.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-49+22634_-49+2264 others(17): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | |||||
| chr21:43926636
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0051g0207a0001c0001t0057g0208 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-49+22633_-49+2264 others(18): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | |||||
| chr21:43926756
|
T | C | 1 | a0001c0001t0003g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-49+22737T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926756 | ||||||
| chr21:43926825
|
G | A | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+22806G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926825 | ||||||
| chr21:43926978
|
C | CA | 39 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0164others(36): Show | 40 | HG00544.hp2 HG01257.hp1 HG01258.hp2 others(37): Show |
intron_variant | MODIFIER | c.-49+22982dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926978 | |||||
| chr21:43926978
|
CA | C | 21 | a0001c0001t0001g0031a0001c0001t0001g0201a0001c0001t0001g0221others(18): Show | 21 | HG01256.hp1 HG01257.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49+22982delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926978 | |||||
| chr21:43927063
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0164 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-49+23044C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43927063 | ||||||
| chr21:43927264
|
T | A | 3 | a0001c0001t0002g0199a0001c0001t0002g0219a0001c0001t0002g0246 | 3 | NA18941.hp1 NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-49+23245T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43927264 | ||||||
| chr21:43927268
|
TG | T | 3 | a0001c0001t0002g0199a0001c0001t0002g0219a0001c0001t0002g0246 | 3 | NA18941.hp1 NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-49+23250delG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43927268 | ||||||
| chr21:43927488
|
T | G | 2 | a0001c0001t0001g0251a0001c0001t0003g0288 | 2 | HG02132.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-49+23469T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43927488 | ||||||
| chr21:43927888
|
G | A | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49+23869G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43927888 | ||||||
| chr21:43928042
|
G | A | 5 | a0001c0001t0006g0205a0001c0001t0007g0192a0001c0001t0051g0207others(2): Show | 5 | HG01081.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+24023G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928042 | ||||||
| chr21:43928058
|
C | T | 1 | a0001c0001t0010g0110 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-49+24039C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928058 | ||||||
| chr21:43928096
|
G | A | 1 | a0001c0001t0019g0330 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-49+24077G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928096 | ||||||
| chr21:43928298
|
A | C | 6 | a0001c0001t0001g0221a0001c0001t0001g0237a0001c0001t0001g0251others(3): Show | 6 | HG02015.hp2 HG02080.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+24279A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928298 | ||||||
| chr21:43928391
|
T | G | 2 | a0001c0001t0005g0082a0001c0001t0035g0303 | 2 | HG01074.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-49+24372T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928391 | ||||||
| chr21:43928482
|
T | G | 234 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-49+24463T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928482 | ||||||
| chr21:43928643
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-49+24624G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928643 | ||||||
| chr21:43928784
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-49+24765G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928784 | ||||||
| chr21:43928788
|
G | A | 2 | a0001c0003t0011g0260a0001c0003t0011g0261 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-49+24769G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928788 | ||||||
| chr21:43928840
|
A | C | 1 | a0001c0001t0004g0317 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-49+24821A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928840 | ||||||
| chr21:43928910
|
A | C | 1 | a0001c0001t0005g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-49+24891A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928910 | ||||||
| chr21:43929057
|
C | T | 1 | a0001c0001t0073g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-49+25038C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929057 | ||||||
| chr21:43929073
|
C | G | 234 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-49+25054C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929073 | ||||||
| chr21:43929092
|
C | T | 2 | a0001c0001t0004g0240a0001c0001t0072g0209 | 2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.-49+25073C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929092 | ||||||
| chr21:43929127
|
A | G | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+25108A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929127 | ||||||
| chr21:43929222
|
G | A | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+25203G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929222 | ||||||
| chr21:43929419
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-49+25400C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929419 | ||||||
| chr21:43929461
|
G | A | 3 | a0001c0001t0033g0212a0001c0001t0074g0211a0001c0001t0077g0254 | 3 | NA18977.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-49+25442G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929461 | ||||||
| chr21:43929513
|
A | G | 8 | a0001c0001t0003g0085a0001c0001t0015g0115a0001c0001t0015g0116others(5): Show | 8 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49+25494A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929513 | ||||||
| chr21:43929544
|
C | T | 12 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(9): Show | 12 | HG00558.hp2 HG00621.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-49+25525C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929544 | ||||||
| chr21:43929595
|
C | A | 1 | a0001c0001t0004g0029 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-49+25576C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929595 | ||||||
| chr21:43929628
|
C | T | 32 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0296others(29): Show | 33 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-49+25609C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929628 | ||||||
| chr21:43929778
|
C | G | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-49+25759C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929778 | ||||||
| chr21:43929779
|
C | T | 1 | a0001c0001t0005g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-49+25760C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929779 | ||||||
| chr21:43929871
|
C | T | 85 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-49+25852C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929871 | ||||||
| chr21:43929875
|
G | A | 239 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.-49+25856G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929875 | ||||||
| chr21:43929903
|
A | G | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+25884A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929903 | ||||||
| chr21:43929925
|
A | G | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+25906A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929925 | ||||||
| chr21:43929942
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-49+25923G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929942 | ||||||
| chr21:43930150
|
G | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-49+26131G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930150 | ||||||
| chr21:43930209
|
C | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-49+26190C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930209 | ||||||
| chr21:43930387
|
G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-49+26368G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930387 | ||||||
| chr21:43930474
|
C | T | 1 | a0001c0001t0017g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49+26455C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930474 | ||||||
| chr21:43930613
|
C | T | 1 | a0001c0001t0032g0325 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-49+26594C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930613 | ||||||
| chr21:43930711
|
C | T | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-49+26692C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930711 | ||||||
| chr21:43930834
|
C | G | 1 | a0001c0001t0015g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-49+26815C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930834 | ||||||
| chr21:43930880
|
G | A | 1 | a0001c0001t0001g0334 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-49+26861G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930880 | ||||||
| chr21:43930888
|
C | T | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+26869C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930888 | ||||||
| chr21:43930972
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0217 | 2 | NA18993.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-49+26953G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930972 | ||||||
| chr21:43931219
|
T | C | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+27200T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931219 | ||||||
| chr21:43931265
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0163 | 2 | HG01256.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-49+27246G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931265 | ||||||
| chr21:43931291
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-49+27272G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931291 | ||||||
| chr21:43931325
|
C | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0292a0001c0001t0004g0240 | 3 | HG00642.hp2 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-49+27306C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931325 | ||||||
| chr21:43931330
|
G | A | 1 | a0001c0001t0058g0315 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-49+27311G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931330 | ||||||
| chr21:43931402
|
C | T | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-49+27383C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931402 | ||||||
| chr21:43931450
|
A | T | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+27431A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931450 | ||||||
| chr21:43931592
|
C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+27573C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931592 | ||||||
| chr21:43931650
|
C | G | 1 | a0001c0001t0017g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49+27631C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931650 | ||||||
| chr21:43931651
|
G | A | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-49+27632G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931651 | ||||||
| chr21:43931725
|
C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-49+27706C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931725 | ||||||
| chr21:43931894
|
C | T | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-48-27740C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931894 | ||||||
| chr21:43931922
|
C | CGT | 21 | a0001c0001t0001g0170a0001c0001t0001g0305a0001c0001t0002g0078others(18): Show | 21 | HG00408.hp1 HG01099.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.-48-27669_-48-2766 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | |||||
| chr21:43931922
|
C | CGTGT | 15 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0003g0002others(12): Show | 16 | HG02258.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-48-27671_-48-2766 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | |||||
| chr21:43931922
|
C | CGTGTGT | 4 | a0001c0001t0003g0121a0001c0001t0003g0125a0001c0001t0031g0196others(1): Show | 4 | HG01257.hp1 HG01258.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-27673_-48-2766 others(10): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | |||||
| chr21:43931922
|
CGT | C | 11 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0003g0181others(8): Show | 11 | HG00323.hp2 HG01433.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-48-27669_-48-2766 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | |||||
| chr21:43931922
|
CGTGT | C | 41 | a0001c0001t0001g0285a0001c0001t0005g0082a0001c0001t0005g0086others(38): Show | 42 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-48-27671_-48-2766 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | |||||
| chr21:43931922
|
CGTGTGT | C | 100 | a0001c0001t0001g0054a0001c0001t0001g0113a0001c0001t0001g0197others(97): Show | 100 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-48-27673_-48-2766 others(10): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | |||||
| chr21:43931922
|
CGTGTGTG others(1): Show |
C | 5 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(2): Show | 5 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-27675_-48-2766 others(12): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | |||||
| chr21:43931922
|
CGTGTGTG others(3): Show |
C | 3 | a0001c0001t0003g0085a0001c0001t0018g0084a0001c0001t0029g0083 | 3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-48-27677_-48-2766 others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | |||||
| chr21:43931922
|
CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0004g0278a0001c0001t0076g0279 | 2 | HG00099.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.-48-27681_-48-2766 others(18): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | |||||
| chr21:43931922
|
CGTGTGTG others(9): Show |
C | 84 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(81): Show | 84 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-48-27683_-48-2766 others(20): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | |||||
| chr21:43931957
|
G | A | 79 | a0001c0001t0001g0054a0001c0001t0001g0113a0001c0001t0001g0197others(76): Show | 79 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-48-27677G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931957 | ||||||
| chr21:43932195
|
C | T | 1 | a0001c0001t0001g0334 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-48-27439C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932195 | ||||||
| chr21:43932207
|
C | A | 1 | a0001c0001t0003g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-48-27427C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932207 | ||||||
| chr21:43932208
|
G | A | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-48-27426G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932208 | ||||||
| chr21:43932260
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-48-27374G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932260 | ||||||
| chr21:43932323
|
C | T | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48-27311C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932323 | ||||||
| chr21:43932329
|
C | T | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-27305C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932329 | ||||||
| chr21:43932366
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-48-27268G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932366 | ||||||
| chr21:43932388
|
C | G | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-48-27246C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932388 | ||||||
| chr21:43932471
|
G | A | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-48-27163G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932471 | ||||||
| chr21:43932572
|
C | T | 1 | a0001c0001t0069g0301 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-48-27062C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932572 | ||||||
| chr21:43932573
|
G | A | 1 | a0001c0001t0004g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-48-27061G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932573 | ||||||
| chr21:43932647
|
TGGTA | T | 5 | a0001c0001t0012g0076a0001c0001t0012g0099a0001c0001t0012g0101others(2): Show | 5 | HG02809.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-26985_-48-2698 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43932647 | |||||
| chr21:43932719
|
C | T | 6 | a0001c0001t0004g0281a0001c0001t0004g0317a0001c0001t0033g0212others(3): Show | 6 | HG00558.hp2 HG02027.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-26915C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932719 | ||||||
| chr21:43932940
|
G | C | 1 | a0001c0001t0003g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-48-26694G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932940 | ||||||
| chr21:43932995
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-48-26639G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932995 | ||||||
| chr21:43933045
|
C | T | 1 | a0001c0001t0063g0273 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-48-26589C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933045 | ||||||
| chr21:43933094
|
A | T | 1 | a0001c0001t0042g0092 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-48-26540A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933094 | ||||||
| chr21:43933230
|
G | A | 32 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0296others(29): Show | 33 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-48-26404G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933230 | ||||||
| chr21:43933278
|
T | C | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-48-26356T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933278 | ||||||
| chr21:43933354
|
G | A | 2 | a0001c0001t0045g0104a0001c0001t0049g0320 | 2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-48-26280G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933354 | ||||||
| chr21:43933389
|
G | A | 1 | a0001c0001t0005g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-48-26245G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933389 | ||||||
| chr21:43933642
|
G | A | 1 | a0001c0001t0073g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-48-25992G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933642 | ||||||
| chr21:43933643
|
G | C | 1 | a0001c0001t0073g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-48-25991G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933643 | ||||||
| chr21:43933644
|
C | T | 1 | a0001c0001t0073g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-48-25990C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933644 | ||||||
| chr21:43933799
|
A | G | 5 | a0001c0001t0006g0205a0001c0001t0007g0192a0001c0001t0051g0207others(2): Show | 5 | HG01081.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-25835A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933799 | ||||||
| chr21:43933827
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0004g0126others(2): Show | 5 | HG01256.hp2 HG01433.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-25807C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933827 | ||||||
| chr21:43933847
|
C | T | 1 | a0001c0001t0059g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-48-25787C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933847 | ||||||
| chr21:43934043
|
G | T | 2 | a0001c0001t0002g0078a0001c0001t0018g0081 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-48-25591G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934043 | ||||||
| chr21:43934140
|
T | C | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-25494T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934140 | ||||||
| chr21:43934169
|
A | G | 1 | a0001c0001t0019g0330 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-48-25465A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934169 | ||||||
| chr21:43934233
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-48-25401C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934233 | ||||||
| chr21:43934274
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-48-25360C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934274 | ||||||
| chr21:43934291
|
C | T | 7 | a0001c0001t0012g0076a0001c0001t0012g0099a0001c0001t0012g0101others(4): Show | 7 | HG01109.hp1 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-25343C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934291 | ||||||
| chr21:43934308
|
G | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-48-25326G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934308 | ||||||
| chr21:43934330
|
C | T | 4 | a0001c0001t0006g0194a0001c0001t0031g0195a0001c0001t0031g0196others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-25304C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934330 | ||||||
| chr21:43934407
|
G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-25227G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934407 | ||||||
| chr21:43934516
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-48-25118C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934516 | ||||||
| chr21:43934558
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-48-25076C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934558 | ||||||
| chr21:43934561
|
G | T | 95 | a0001c0001t0001g0054a0001c0001t0001g0113a0001c0001t0001g0197others(92): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-48-25073G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934561 | ||||||
| chr21:43934712
|
G | A | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-48-24922G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934712 | ||||||
| chr21:43934742
|
G | A | 5 | a0001c0001t0001g0225a0001c0001t0004g0188a0001c0001t0004g0190others(2): Show | 5 | HG01943.hp1 HG01978.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-24892G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934742 | ||||||
| chr21:43934795
|
C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-48-24839C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934795 | ||||||
| chr21:43934837
|
C | T | 4 | a0001c0001t0006g0194a0001c0001t0031g0195a0001c0001t0031g0196others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-24797C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934837 | ||||||
| chr21:43934840
|
C | T | 1 | a0001c0001t0008g0143 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-48-24794C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934840 | ||||||
| chr21:43934863
|
G | A | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-48-24771G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934863 | ||||||
| chr21:43934973
|
C | T | 1 | a0001c0001t0004g0044 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-48-24661C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934973 | ||||||
| chr21:43935039
|
G | A | 1 | a0001c0001t0003g0128 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-48-24595G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935039 | ||||||
| chr21:43935050
|
C | G | 1 | a0001c0001t0004g0312 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-48-24584C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935050 | ||||||
| chr21:43935060
|
C | T | 1 | a0001c0001t0009g0226 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-48-24574C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935060 | ||||||
| chr21:43935096
|
G | T | 1 | a0001c0001t0050g0024 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-48-24538G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935096 | ||||||
| chr21:43935138
|
G | A | 1 | a0001c0009t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-48-24496G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935138 | ||||||
| chr21:43935245
|
C | A | 2 | a0001c0001t0002g0078a0001c0001t0018g0081 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-48-24389C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935245 | ||||||
| chr21:43935276
|
C | T | 1 | a0001c0001t0002g0339 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-48-24358C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935276 | ||||||
| chr21:43935286
|
G | A | 230 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.-48-24348G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935286 | ||||||
| chr21:43935436
|
G | C | 4 | a0001c0001t0001g0300a0001c0001t0001g0334a0001c0001t0004g0012others(1): Show | 4 | HG00597.hp1 HG02074.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-24198G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935436 | ||||||
| chr21:43935531
|
C | T | 32 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0296others(29): Show | 33 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-48-24103C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935531 | ||||||
| chr21:43935611
|
G | T | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-48-24023G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935611 | ||||||
| chr21:43935644
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-48-23990G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935644 | ||||||
| chr21:43935648
|
T | C | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-48-23986T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935648 | ||||||
| chr21:43935730
|
C | T | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-23904C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935730 | ||||||
| chr21:43935947
|
C | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-48-23687C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935947 | ||||||
| chr21:43935952
|
C | T | 142 | a0001c0001t0001g0054a0001c0001t0001g0113a0001c0001t0001g0197others(139): Show | 143 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.-48-23682C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935952 | ||||||
| chr21:43936045
|
C | T | 1 | a0001c0001t0016g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-48-23589C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936045 | ||||||
| chr21:43936135
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-48-23499G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936135 | ||||||
| chr21:43936192
|
T | G | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-48-23442T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936192 | ||||||
| chr21:43936279
|
C | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-23355C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936279 | ||||||
| chr21:43936302
|
A | G | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-48-23332A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936302 | ||||||
| chr21:43936506
|
C | T | 1 | a0001c0001t0003g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-48-23128C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936506 | ||||||
| chr21:43936606
|
C | T | 143 | a0001c0001t0001g0054a0001c0001t0001g0113a0001c0001t0001g0197others(140): Show | 144 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-48-23028C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936606 | ||||||
| chr21:43936703
|
T | G | 1 | a0001c0001t0022g0051 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-48-22931T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936703 | ||||||
| chr21:43936832
|
C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-22802C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936832 | ||||||
| chr21:43936907
|
T | G | 2 | a0001c0001t0013g0005a0001c0001t0013g0006 | 2 | HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-48-22727T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936907 | ||||||
| chr21:43937014
|
T | G | 1 | a0001c0001t0008g0159 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-48-22620T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937014 | ||||||
| chr21:43937094
|
G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-22540G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937094 | ||||||
| chr21:43937285
|
C | G | 1 | a0001c0001t0023g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-48-22349C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937285 | ||||||
| chr21:43937368
|
C | T | 1 | a0001c0001t0002g0060 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-48-22266C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937368 | ||||||
| chr21:43937375
|
G | A | 5 | a0001c0001t0019g0069a0001c0001t0019g0323a0001c0001t0019g0330others(2): Show | 5 | HG02055.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-22259G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937375 | ||||||
| chr21:43937404
|
C | T | 28 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(25): Show | 28 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.-48-22230C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937404 | ||||||
| chr21:43937418
|
C | G | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-48-22216C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937418 | ||||||
| chr21:43937420
|
A | G | 231 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-48-22214A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937420 | ||||||
| chr21:43937556
|
T | G | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-22078T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937556 | ||||||
| chr21:43937684
|
A | G | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-21950A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937684 | ||||||
| chr21:43937849
|
A | G | 32 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0296others(29): Show | 33 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-48-21785A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937849 | ||||||
| chr21:43938085
|
TTC | T | 222 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-48-21530_-48-2152 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938085 | |||||
| chr21:43938104
|
T | A | 14 | a0001c0001t0006g0194a0001c0001t0006g0205a0001c0001t0007g0192others(11): Show | 14 | HG01081.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48-21530T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938104 | ||||||
| chr21:43938106
|
A | T | 1 | a0001c0001t0001g0269 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-48-21528A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938106 | ||||||
| chr21:43938111
|
C | CACAG | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0057g0208others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-21520_-48-2151 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938111 | |||||
| chr21:43938115
|
C | G | 8 | a0001c0001t0003g0161a0001c0001t0006g0194a0001c0001t0020g0064others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48-21519C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938115 | ||||||
| chr21:43938117
|
G | C | 15 | a0001c0001t0003g0161a0001c0001t0006g0194a0001c0001t0006g0205others(12): Show | 15 | HG01081.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-48-21517G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938117 | ||||||
| chr21:43938117
|
G | GAC | 37 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0155others(34): Show | 38 | HG00280.hp1 HG00544.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.-48-21494_-48-2149 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938117 | |||||
| chr21:43938117
|
GACAC | G | 80 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-48-21496_-48-2149 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938117 | |||||
| chr21:43938117
|
GACACACA others(3): Show |
G | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-48-21502_-48-2149 others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938117 | |||||
| chr21:43938276
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0004g0286a0001c0001t0004g0314 | 3 | HG00741.hp1 HG01192.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-48-21358G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938276 | ||||||
| chr21:43938316
|
C | CT | 10 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0157others(7): Show | 10 | HG01256.hp2 HG02055.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.-48-21293dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938316 | |||||
| chr21:43938316
|
CT | C | 20 | a0001c0001t0001g0265a0001c0001t0002g0060a0001c0001t0002g0078others(17): Show | 20 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-48-21293delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938316 | |||||
| chr21:43938316
|
CTT | C | 221 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-48-21294_-48-2129 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938316 | |||||
| chr21:43938316
|
CTTT | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0057others(7): Show | 10 | HG01070.hp2 HG01256.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48-21295_-48-2129 others(7): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938316 | |||||
| chr21:43938316
|
CTTTTTTT others(1): Show |
C | 28 | a0001c0001t0002g0296a0001c0001t0002g0307a0001c0001t0003g0002others(25): Show | 29 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-48-21300_-48-2129 others(12): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938316 | |||||
| chr21:43938360
|
T | C | 4 | a0001c0001t0006g0194a0001c0001t0031g0195a0001c0001t0031g0196others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-21274T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938360 | ||||||
| chr21:43938394
|
G | C | 1 | a0001c0001t0008g0158 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-48-21240G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938394 | ||||||
| chr21:43938453
|
A | G | 1 | a0001c0001t0002g0132 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-48-21181A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938453 | ||||||
| chr21:43938546
|
G | A | 1 | a0001c0001t0004g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-48-21088G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938546 | ||||||
| chr21:43938584
|
G | A | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-48-21050G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938584 | ||||||
| chr21:43938781
|
C | T | 14 | a0001c0001t0003g0085a0001c0001t0015g0115a0001c0001t0015g0116others(11): Show | 14 | HG01261.hp2 HG01496.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48-20853C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938781 | ||||||
| chr21:43938815
|
C | T | 1 | a0001c0001t0003g0288 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-48-20819C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938815 | ||||||
| chr21:43938925
|
C | T | 47 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0034others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-48-20709C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938925 | ||||||
| chr21:43938943
|
C | G | 1 | a0001c0001t0064g0147 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-48-20691C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938943 | ||||||
| chr21:43939042
|
G | A | 9 | a0001c0001t0006g0205a0001c0001t0012g0076a0001c0001t0012g0099others(6): Show | 9 | HG01081.hp1 HG01891.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-20592G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939042 | ||||||
| chr21:43939078
|
C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-48-20556C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939078 | ||||||
| chr21:43939114
|
T | C | 5 | a0001c0001t0001g0165a0001c0001t0005g0088a0001c0001t0005g0089others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-20520T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939114 | ||||||
| chr21:43939127
|
G | T | 36 | a0001c0001t0005g0082a0001c0001t0005g0088a0001c0001t0005g0089others(33): Show | 36 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-48-20507G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939127 | ||||||
| chr21:43939217
|
G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-20417G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939217 | ||||||
| chr21:43939464
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG01070.hp2 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-48-20170C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939464 | ||||||
| chr21:43939592
|
C | T | 7 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(4): Show | 7 | HG01109.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-20042C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939592 | ||||||
| chr21:43939687
|
C | G | 1 | a0001c0001t0001g0184 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-48-19947C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939687 | ||||||
| chr21:43939706
|
C | T | 126 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0054others(123): Show | 127 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-48-19928C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939706 | ||||||
| chr21:43939927
|
G | A | 34 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0078others(31): Show | 35 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-48-19707G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939927 | ||||||
| chr21:43939943
|
G | C | 6 | a0001c0001t0001g0200a0001c0001t0001g0222a0001c0001t0001g0243others(3): Show | 6 | HG01261.hp1 HG01346.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-19691G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939943 | ||||||
| chr21:43939949
|
C | T | 1 | a0001c0001t0038g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-48-19685C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939949 | ||||||
| chr21:43939959
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-48-19675C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939959 | ||||||
| chr21:43939989
|
G | A | 2 | a0001c0003t0011g0260a0001c0003t0011g0261 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-48-19645G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939989 | ||||||
| chr21:43940145
|
A | C | 2 | a0001c0001t0012g0076a0001c0001t0012g0101 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-48-19489A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940145 | ||||||
| chr21:43940164
|
G | A | 12 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(9): Show | 12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-19470G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940164 | ||||||
| chr21:43940217
|
G | C | 1 | a0001c0001t0046g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-48-19417G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940217 | ||||||
| chr21:43940513
|
G | C | 40 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0078others(37): Show | 41 | HG00544.hp2 HG01257.hp1 HG01258.hp2 others(38): Show |
intron_variant | MODIFIER | c.-48-19121G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940513 | ||||||
| chr21:43940582
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48-19052C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940582 | ||||||
| chr21:43940635
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-48-18999G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940635 | ||||||
| chr21:43940814
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-48-18820C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940814 | ||||||
| chr21:43940838
|
G | A | 7 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(4): Show | 7 | HG01109.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-18796G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940838 | ||||||
| chr21:43940934
|
C | T | 1 | a0001c0001t0004g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-48-18700C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940934 | ||||||
| chr21:43940981
|
G | A | 91 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.-48-18653G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940981 | ||||||
| chr21:43941001
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0223 | 2 | NA18977.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-48-18633A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941001 | ||||||
| chr21:43941163
|
A | G | 244 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.-48-18471A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941163 | ||||||
| chr21:43941186
|
A | G | 12 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(9): Show | 12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-18448A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941186 | ||||||
| chr21:43941214
|
C | T | 244 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.-48-18420C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941214 | ||||||
| chr21:43941234
|
GCA | G | 3 | a0001c0001t0003g0153a0001c0001t0003g0167a0001c0001t0007g0154 | 3 | NA18945.hp2 NA19009.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-48-18396_-48-1839 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43941234 | |||||
| chr21:43941377
|
G | T | 1 | a0001c0001t0002g0332 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-48-18257G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941377 | ||||||
| chr21:43941444
|
G | C | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-48-18190G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941444 | ||||||
| chr21:43941446
|
C | T | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48-18188C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941446 | ||||||
| chr21:43941515
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG01070.hp2 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-48-18119C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941515 | ||||||
| chr21:43941620
|
G | C | 34 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0078others(31): Show | 35 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-48-18014G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941620 | ||||||
| chr21:43941778
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48-17856C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941778 | ||||||
| chr21:43941791
|
G | A | 2 | a0001c0001t0002g0199a0001c0001t0002g0246 | 2 | NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-48-17843G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941791 | ||||||
| chr21:43942094
|
G | C | 5 | a0001c0001t0007g0192a0001c0001t0007g0326a0001c0001t0007g0327others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-17540G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942094 | ||||||
| chr21:43942108
|
C | T | 1 | a0001c0001t0002g0189 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-48-17526C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942108 | ||||||
| chr21:43942117
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0032g0324a0001c0001t0032g0325 | 3 | HG00280.hp2 HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-17517G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942117 | ||||||
| chr21:43942295
|
G | A | 5 | a0001c0001t0031g0195a0001c0001t0031g0196a0001c0001t0049g0320others(2): Show | 5 | HG01257.hp1 HG01258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-17339G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942295 | ||||||
| chr21:43942409
|
C | T | 1 | a0001c0001t0006g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-48-17225C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942409 | ||||||
| chr21:43942442
|
G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-17192G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942442 | ||||||
| chr21:43942557
|
G | C | 10 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-48-17077G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942557 | ||||||
| chr21:43942608
|
G | C | 144 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0054others(141): Show | 145 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-48-17026G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942608 | ||||||
| chr21:43942718
|
C | T | 6 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0046others(3): Show | 6 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-16916C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942718 | ||||||
| chr21:43942722
|
G | A | 4 | a0001c0001t0006g0205a0001c0001t0051g0207a0001c0001t0072g0209others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-16912G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942722 | ||||||
| chr21:43942739
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-48-16895C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942739 | ||||||
| chr21:43942845
|
G | T | 7 | a0001c0001t0006g0205a0001c0001t0010g0063a0001c0001t0010g0095others(4): Show | 7 | HG00639.hp1 HG01081.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-16789G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942845 | ||||||
| chr21:43943091
|
G | A | 3 | a0001c0001t0010g0063a0001c0001t0010g0095a0001c0001t0010g0096 | 3 | HG00639.hp1 HG04228.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-48-16543G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943091 | ||||||
| chr21:43943165
|
C | T | 7 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(4): Show | 7 | HG01109.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-16469C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943165 | ||||||
| chr21:43943199
|
C | T | 12 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(9): Show | 12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-16435C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943199 | ||||||
| chr21:43943235
|
C | T | 1 | a0001c0001t0015g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-48-16399C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943235 | ||||||
| chr21:43943265
|
G | A | 12 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(9): Show | 12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-16369G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943265 | ||||||
| chr21:43943370
|
A | T | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-48-16264A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943370 | ||||||
| chr21:43943415
|
C | T | 1 | a0001c0001t0059g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-48-16219C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943415 | ||||||
| chr21:43943515
|
T | C | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-48-16119T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943515 | ||||||
| chr21:43943536
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-48-16098C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943536 | ||||||
| chr21:43943570
|
G | T | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-16064G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943570 | ||||||
| chr21:43943581
|
A | T | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-16053A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943581 | ||||||
| chr21:43943641
|
G | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.-48-15993G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943641 | ||||||
| chr21:43943714
|
C | T | 1 | a0001c0001t0017g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-48-15920C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943714 | ||||||
| chr21:43943801
|
C | T | 1 | a0001c0001t0008g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-48-15833C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943801 | ||||||
| chr21:43943894
|
C | T | 1 | a0001c0001t0039g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-48-15740C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943894 | ||||||
| chr21:43943915
|
G | A | 1 | a0001c0001t0003g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-48-15719G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943915 | ||||||
| chr21:43943936
|
G | C | 7 | a0001c0001t0006g0074a0001c0001t0031g0195a0001c0001t0031g0196others(4): Show | 7 | HG01257.hp1 HG01258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-15698G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943936 | ||||||
| chr21:43944016
|
A | G | 148 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0054others(145): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-48-15618A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944016 | ||||||
| chr21:43944024
|
G | A | 147 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0054others(144): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-48-15610G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944024 | ||||||
| chr21:43944055
|
A | G | 2 | a0001c0001t0017g0098a0001c0002t0048g0298 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-48-15579A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944055 | ||||||
| chr21:43944160
|
C | T | 2 | a0001c0001t0030g0073a0001c0001t0030g0331 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-48-15474C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944160 | ||||||
| chr21:43944165
|
C | T | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-48-15469C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944165 | ||||||
| chr21:43944173
|
G | A | 7 | a0001c0001t0006g0074a0001c0001t0031g0195a0001c0001t0031g0196others(4): Show | 7 | HG01257.hp1 HG01258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-15461G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944173 | ||||||
| chr21:43944329
|
G | C | 12 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(9): Show | 12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-15305G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944329 | ||||||
| chr21:43944394
|
G | A | 1 | a0001c0001t0004g0047 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-48-15240G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944394 | ||||||
| chr21:43944605
|
A | C | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-48-15029A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944605 | ||||||
| chr21:43944606
|
G | C | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-48-15028G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944606 | ||||||
| chr21:43944656
|
C | T | 1 | a0001c0001t0004g0244 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-48-14978C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944656 | ||||||
| chr21:43944789
|
C | T | 2 | a0001c0001t0005g0322a0002c0006t0010g0112 | 2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-48-14845C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944789 | ||||||
| chr21:43944807
|
A | G | 1 | a0001c0001t0032g0325 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-48-14827A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944807 | ||||||
| chr21:43944930
|
G | A | 1 | a0001c0002t0018g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-48-14704G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944930 | ||||||
| chr21:43944959
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-48-14675C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944959 | ||||||
| chr21:43944968
|
A | G | 2 | a0001c0001t0074g0211a0001c0001t0077g0254 | 2 | NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-48-14666A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944968 | ||||||
| chr21:43945064
|
G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-14570G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945064 | ||||||
| chr21:43945076
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-48-14558G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945076 | ||||||
| chr21:43945119
|
A | G | 3 | a0001c0001t0006g0061a0001c0001t0022g0055a0001c0001t0073g0053 | 3 | HG01167.hp1 HG02818.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-48-14515A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945119 | ||||||
| chr21:43945140
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0237a0001c0001t0001g0268others(1): Show | 4 | HG02015.hp2 HG02080.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-14494G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945140 | ||||||
| chr21:43945227
|
C | T | 4 | a0001c0001t0001g0206a0001c0001t0013g0239a0001c0003t0011g0260others(1): Show | 4 | HG00140.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-14407C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945227 | ||||||
| chr21:43945328
|
T | C | 300 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(297): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.-48-14306T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945328 | ||||||
| chr21:43945367
|
G | C | 95 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.-48-14267G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945367 | ||||||
| chr21:43945385
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-48-14249C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945385 | ||||||
| chr21:43945420
|
T | C | 4 | a0001c0001t0010g0063a0001c0001t0010g0095a0001c0001t0010g0096others(1): Show | 4 | HG00639.hp1 HG01884.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-14214T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945420 | ||||||
| chr21:43945501
|
C | T | 1 | a0001c0001t0079g0228 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-48-14133C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945501 | ||||||
| chr21:43945784
|
G | T | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48-13850G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945784 | ||||||
| chr21:43945932
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-48-13702G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945932 | ||||||
| chr21:43945956
|
G | A | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-48-13678G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945956 | ||||||
| chr21:43945984
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-48-13650C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945984 | ||||||
| chr21:43946044
|
C | G | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-13590C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946044 | ||||||
| chr21:43946170
|
G | A | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-48-13464G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946170 | ||||||
| chr21:43946193
|
T | TA | 4 | a0001c0001t0010g0063a0001c0001t0010g0095a0001c0001t0010g0096others(1): Show | 4 | HG00639.hp1 HG01884.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-13440dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43946193 | |||||
| chr21:43946238
|
T | C | 2 | a0001c0001t0001g0179a0001c0001t0076g0279 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.-48-13396T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946238 | ||||||
| chr21:43946530
|
G | A | 1 | a0001c0001t0029g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-48-13104G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946530 | ||||||
| chr21:43946599
|
TA | T | 16 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0142others(13): Show | 16 | HG01070.hp2 HG01168.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-48-13019delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43946599 | |||||
| chr21:43946705
|
G | A | 3 | a0001c0001t0031g0195a0001c0001t0031g0196a0001c0001t0062g0313 | 3 | HG01257.hp1 HG01258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-48-12929G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946705 | ||||||
| chr21:43946807
|
T | C | 1 | a0001c0001t0081g0136 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-48-12827T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946807 | ||||||
| chr21:43946880
|
A | G | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-12754A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946880 | ||||||
| chr21:43946998
|
C | T | 6 | a0001c0001t0012g0076a0001c0001t0012g0099a0001c0001t0012g0101others(3): Show | 6 | HG02809.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-12636C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946998 | ||||||
| chr21:43947012
|
A | G | 145 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0054others(142): Show | 146 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-48-12622A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947012 | ||||||
| chr21:43947086
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0300 | 2 | HG00597.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-48-12548A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947086 | ||||||
| chr21:43947143
|
G | A | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-48-12491G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947143 | ||||||
| chr21:43947201
|
T | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0276 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-48-12433T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947201 | ||||||
| chr21:43947271
|
C | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0054others(147): Show | 151 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-48-12363C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947271 | ||||||
| chr21:43947358
|
A | C | 17 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(14): Show | 17 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48-12276A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947358 | ||||||
| chr21:43947361
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-48-12273C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947361 | ||||||
| chr21:43947391
|
A | G | 12 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(9): Show | 12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-12243A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947391 | ||||||
| chr21:43947419
|
G | A | 42 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0078others(39): Show | 43 | HG00544.hp2 HG01257.hp1 HG01258.hp2 others(40): Show |
intron_variant | MODIFIER | c.-48-12215G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947419 | ||||||
| chr21:43947474
|
G | A | 12 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(9): Show | 12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-12160G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947474 | ||||||
| chr21:43947545
|
G | C | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-48-12089G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947545 | ||||||
| chr21:43947583
|
G | A | 94 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.-48-12051G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947583 | ||||||
| chr21:43947634
|
C | T | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-48-12000C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947634 | ||||||
| chr21:43947668
|
C | A | 4 | a0001c0001t0001g0206a0001c0001t0013g0239a0001c0003t0011g0260others(1): Show | 4 | HG00140.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-11966C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947668 | ||||||
| chr21:43947692
|
C | CT | 94 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.-48-11928dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43947692 | |||||
| chr21:43947745
|
G | A | 107 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.-48-11889G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947745 | ||||||
| chr21:43947787
|
G | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48-11847G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947787 | ||||||
| chr21:43947788
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48-11846C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947788 | ||||||
| chr21:43947801
|
A | T | 1 | a0001c0001t0015g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-48-11833A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947801 | ||||||
| chr21:43947812
|
T | G | 1 | a0001c0001t0001g0334 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-48-11822T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947812 | ||||||
| chr21:43947898
|
T | C | 1 | a0001c0001t0003g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-48-11736T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947898 | ||||||
| chr21:43948066
|
G | T | 1 | a0001c0001t0004g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-48-11568G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948066 | ||||||
| chr21:43948322
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0237a0001c0001t0001g0268others(1): Show | 4 | HG02015.hp2 HG02080.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-11312C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948322 | ||||||
| chr21:43948419
|
C | A | 134 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0054others(131): Show | 135 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-48-11215C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948419 | ||||||
| chr21:43948420
|
A | G | 134 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0054others(131): Show | 135 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-48-11214A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948420 | ||||||
| chr21:43948421
|
C | A | 134 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0054others(131): Show | 135 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-48-11213C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948421 | ||||||
| chr21:43948557
|
A | C | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-11077A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948557 | ||||||
| chr21:43948560
|
G | C | 6 | a0001c0001t0001g0221a0001c0001t0001g0237a0001c0001t0001g0268others(3): Show | 6 | HG01243.hp2 HG02015.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-11074G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948560 | ||||||
| chr21:43948610
|
G | A | 314 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-48-11024G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948610 | ||||||
| chr21:43948622
|
T | C | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-48-11012T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948622 | ||||||
| chr21:43948649
|
A | G | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0162others(1): Show | 4 | NA18747.hp2 NA18955.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-10985A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948649 | ||||||
| chr21:43948711
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48-10923C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948711 | ||||||
| chr21:43948726
|
G | C | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-10908G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948726 | ||||||
| chr21:43948827
|
C | T | 2 | a0001c0001t0030g0073a0001c0001t0030g0331 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-48-10807C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948827 | ||||||
| chr21:43948862
|
C | T | 1 | a0001c0001t0021g0262 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-48-10772C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948862 | ||||||
| chr21:43948883
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-48-10751C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948883 | ||||||
| chr21:43948978
|
G | T | 2 | a0001c0001t0005g0322a0002c0006t0010g0112 | 2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-48-10656G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948978 | ||||||
| chr21:43948982
|
A | G | 2 | a0001c0001t0006g0205a0001c0001t0072g0209 | 2 | HG01081.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-48-10652A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948982 | ||||||
| chr21:43948992
|
C | T | 33 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0078others(30): Show | 34 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-48-10642C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948992 | ||||||
| chr21:43949004
|
G | A | 238 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-48-10630G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949004 | ||||||
| chr21:43949266
|
G | A | 41 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0078others(38): Show | 42 | HG00544.hp2 HG01257.hp1 HG01258.hp2 others(39): Show |
intron_variant | MODIFIER | c.-48-10368G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949266 | ||||||
| chr21:43949359
|
G | A | 14 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0210others(11): Show | 14 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48-10275G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949359 | ||||||
| chr21:43949553
|
A | G | 207 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-48-10081A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949553 | ||||||
| chr21:43949606
|
G | T | 79 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0148others(76): Show | 80 | HG00323.hp2 HG00438.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-48-10028G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949606 | ||||||
| chr21:43949638
|
G | T | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-48-9996G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949638 | ||||||
| chr21:43949654
|
G | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0028others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.-48-9980G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949654 | ||||||
| chr21:43949768
|
G | A | 1 | a0001c0001t0076g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-48-9866G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949768 | ||||||
| chr21:43949792
|
T | G | 1 | a0001c0001t0001g0309 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-48-9842T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949792 | ||||||
| chr21:43949931
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48-9703G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949931 | ||||||
| chr21:43949992
|
T | G | 16 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(13): Show | 16 | HG01081.hp1 HG01243.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-48-9642T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949992 | ||||||
| chr21:43950091
|
A | G | 1 | a0001c0001t0059g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-48-9543A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950091 | ||||||
| chr21:43950117
|
A | G | 78 | a0001c0001t0001g0253a0001c0001t0001g0297a0001c0001t0002g0132others(75): Show | 78 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-48-9517A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950117 | ||||||
| chr21:43950304
|
A | G | 6 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(3): Show | 6 | HG02257.hp1 HG02622.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-9330A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950304 | ||||||
| chr21:43950472
|
T | G | 8 | a0001c0001t0001g0113a0001c0001t0001g0197a0001c0001t0001g0231others(5): Show | 8 | HG00408.hp2 HG00423.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48-9162T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950472 | ||||||
| chr21:43950523
|
G | C | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-9111G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950523 | ||||||
| chr21:43950580
|
G | A | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-9054G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950580 | ||||||
| chr21:43950584
|
G | A | 5 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(2): Show | 5 | HG01081.hp1 HG01261.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-9050G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950584 | ||||||
| chr21:43950626
|
G | A | 5 | a0001c0001t0001g0046a0001c0001t0003g0080a0001c0001t0003g0121others(2): Show | 5 | HG01168.hp2 NA18974.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-9008G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950626 | ||||||
| chr21:43950686
|
G | A | 16 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0008g0039others(13): Show | 16 | HG00323.hp2 HG01175.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48-8948G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950686 | ||||||
| chr21:43950698
|
T | C | 2 | a0001c0001t0074g0211a0001c0001t0077g0254 | 2 | NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-48-8936T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950698 | ||||||
| chr21:43950833
|
C | T | 2 | a0001c0001t0004g0286a0001c0001t0004g0314 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-48-8801C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950833 | ||||||
| chr21:43950834
|
G | A | 38 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0001g0297others(35): Show | 39 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(36): Show |
intron_variant | MODIFIER | c.-48-8800G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950834 | ||||||
| chr21:43951007
|
A | G | 182 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0036others(179): Show | 184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.-48-8627A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951007 | ||||||
| chr21:43951146
|
T | C | 6 | a0001c0001t0019g0069a0001c0001t0019g0323a0001c0001t0019g0330others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-8488T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951146 | ||||||
| chr21:43951156
|
TCG | T | 13 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(10): Show | 13 | HG01081.hp1 HG01109.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.-48-8476_-48-8475d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43951156 | |||||
| chr21:43951158
|
G | A | 95 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0163others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-48-8476G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951158 | ||||||
| chr21:43951176
|
C | T | 4 | a0001c0001t0015g0118a0001c0001t0050g0024a0001c0002t0018g0114others(1): Show | 4 | HG02109.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-8458C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951176 | ||||||
| chr21:43951213
|
C | T | 2 | a0001c0001t0028g0242a0001c0001t0063g0273 | 2 | NA18962.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-48-8421C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951213 | ||||||
| chr21:43951286
|
T | C | 1 | a0001c0001t0009g0030 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-48-8348T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951286 | ||||||
| chr21:43951321
|
A | G | 4 | a0001c0001t0036g0094a0001c0001t0037g0304a0001c0001t0038g0109others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-8313A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951321 | ||||||
| chr21:43951447
|
G | A | 110 | a0001c0001t0001g0152a0001c0001t0001g0162a0001c0001t0001g0163others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-48-8187G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951447 | ||||||
| chr21:43951540
|
A | G | 1 | a0001c0001t0004g0012 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-48-8094A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951540 | ||||||
| chr21:43951727
|
A | G | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-7907A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951727 | ||||||
| chr21:43951753
|
C | T | 6 | a0001c0001t0019g0069a0001c0001t0019g0323a0001c0001t0019g0330others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-7881C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951753 | ||||||
| chr21:43951915
|
G | T | 1 | a0001c0001t0004g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-48-7719G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951915 | ||||||
| chr21:43952059
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-48-7575G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952059 | ||||||
| chr21:43952122
|
G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-7512G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952122 | ||||||
| chr21:43952308
|
G | A | 1 | a0001c0001t0005g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-48-7326G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952308 | ||||||
| chr21:43952339
|
A | G | 140 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0162others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-48-7295A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952339 | ||||||
| chr21:43952434
|
G | A | 1 | a0001c0001t0072g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-48-7200G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952434 | ||||||
| chr21:43952556
|
C | T | 2 | a0001c0002t0018g0114a0001c0002t0048g0298 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-48-7078C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952556 | ||||||
| chr21:43952598
|
C | G | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48-7036C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952598 | ||||||
| chr21:43952605
|
C | A | 3 | a0001c0001t0017g0098a0001c0001t0029g0083a0001c0001t0029g0144 | 3 | HG02486.hp2 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-48-7029C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952605 | ||||||
| chr21:43952628
|
G | A | 4 | a0001c0001t0005g0322a0001c0001t0032g0324a0001c0001t0032g0325others(1): Show | 4 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-7006G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952628 | ||||||
| chr21:43952895
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-48-6739G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952895 | ||||||
| chr21:43952932
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-48-6702C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952932 | ||||||
| chr21:43952937
|
T | C | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-6697T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952937 | ||||||
| chr21:43952973
|
A | C | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-6661A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952973 | ||||||
| chr21:43953139
|
A | G | 140 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0162others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-48-6495A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953139 | ||||||
| chr21:43953155
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48-6479C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953155 | ||||||
| chr21:43953165
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-48-6469C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953165 | ||||||
| chr21:43953203
|
G | C | 1 | a0001c0001t0003g0181 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-48-6431G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953203 | ||||||
| chr21:43953312
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0245 | 2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-48-6322G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953312 | ||||||
| chr21:43953423
|
C | T | 42 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0001g0297others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(40): Show |
intron_variant | MODIFIER | c.-48-6211C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953423 | ||||||
| chr21:43953475
|
G | T | 185 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0152others(182): Show | 186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.-48-6159G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953475 | ||||||
| chr21:43953581
|
A | G | 1 | a0001c0001t0015g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-48-6053A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953581 | ||||||
| chr21:43953755
|
G | A | 1 | a0001c0001t0004g0047 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-48-5879G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953755 | ||||||
| chr21:43954119
|
A | G | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-5515A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954119 | ||||||
| chr21:43954398
|
G | A | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-48-5236G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954398 | ||||||
| chr21:43954541
|
C | T | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-5093C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954541 | ||||||
| chr21:43954673
|
G | A | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-4961G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954673 | ||||||
| chr21:43954709
|
A | G | 1 | a0001c0001t0008g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-48-4925A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954709 | ||||||
| chr21:43954863
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-48-4771A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954863 | ||||||
| chr21:43955025
|
C | T | 2 | a0001c0001t0011g0021a0001c0001t0011g0204 | 2 | NA18955.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-48-4609C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955025 | ||||||
| chr21:43955026
|
G | C | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-4608G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955026 | ||||||
| chr21:43955085
|
G | A | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48-4549G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955085 | ||||||
| chr21:43955110
|
G | A | 1 | a0001c0001t0069g0301 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-48-4524G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955110 | ||||||
| chr21:43955184
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-48-4450G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955184 | ||||||
| chr21:43955293
|
G | A | 11 | a0001c0001t0001g0048a0001c0001t0005g0082a0001c0001t0005g0086others(8): Show | 12 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-4341G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955293 | ||||||
| chr21:43955375
|
A | G | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | HG01167.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-48-4259A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955375 | ||||||
| chr21:43955406
|
C | T | 5 | a0001c0001t0004g0079a0001c0001t0004g0126a0001c0001t0004g0286others(2): Show | 5 | HG00741.hp1 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-4228C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955406 | ||||||
| chr21:43955587
|
C | T | 1 | a0001c0001t0007g0326 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-48-4047C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955587 | ||||||
| chr21:43955618
|
C | T | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-48-4016C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955618 | ||||||
| chr21:43955619
|
G | A | 3 | a0001c0001t0030g0073a0001c0001t0030g0331a0001c0001t0050g0024 | 3 | HG02257.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-48-4015G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955619 | ||||||
| chr21:43955621
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-48-4013C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955621 | ||||||
| chr21:43955749
|
T | C | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-3885T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955749 | ||||||
| chr21:43955866
|
C | CTCTAACC others(25): Show |
1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48-3767_-48-3736d others(34): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43955866 | |||||
| chr21:43955880
|
A | T | 182 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0152others(179): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-48-3754A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955880 | ||||||
| chr21:43955899
|
C | CA | 68 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0150others(65): Show | 69 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-48-3718dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43955899 | |||||
| chr21:43955899
|
CA | C | 11 | a0001c0001t0001g0215a0001c0001t0002g0189a0001c0001t0020g0064others(8): Show | 11 | HG02129.hp1 HG02523.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-48-3718delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43955899 | |||||
| chr21:43955938
|
C | T | 4 | a0001c0001t0006g0097a0001c0001t0041g0091a0001c0001t0055g0318others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-3696C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955938 | ||||||
| chr21:43955939
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-48-3695G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955939 | ||||||
| chr21:43955962
|
G | C | 2 | a0001c0001t0003g0080a0001c0001t0003g0161 | 2 | NA18998.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-48-3672G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955962 | ||||||
| chr21:43956048
|
G | A | 1 | a0001c0001t0004g0244 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-48-3586G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956048 | ||||||
| chr21:43956256
|
C | G | 2 | a0001c0002t0018g0114a0001c0002t0048g0298 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-48-3378C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956256 | ||||||
| chr21:43956326
|
A | G | 188 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0152others(185): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.-48-3308A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956326 | ||||||
| chr21:43956489
|
C | T | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-3145C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956489 | ||||||
| chr21:43956556
|
A | T | 1 | a0001c0001t0002g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-48-3078A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956556 | ||||||
| chr21:43956615
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-48-3019C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956615 | ||||||
| chr21:43956792
|
G | A | 24 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0168others(21): Show | 24 | HG00323.hp2 HG01175.hp1 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.-48-2842G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956792 | ||||||
| chr21:43956835
|
A | G | 116 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0179others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48-2799A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956835 | ||||||
| chr21:43956858
|
A | G | 182 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0152others(179): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-48-2776A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956858 | ||||||
| chr21:43957043
|
C | T | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-48-2591C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957043 | ||||||
| chr21:43957151
|
C | T | 3 | a0001c0001t0011g0166a0001c0002t0018g0114a0001c0002t0048g0298 | 3 | HG02040.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-48-2483C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957151 | ||||||
| chr21:43957251
|
C | T | 5 | a0001c0001t0001g0210a0001c0001t0001g0223a0001c0001t0001g0255others(2): Show | 5 | HG00621.hp1 NA18968.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-2383C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957251 | ||||||
| chr21:43957254
|
G | A | 140 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0163others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-48-2380G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957254 | ||||||
| chr21:43957446
|
C | T | 46 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0001g0297others(43): Show | 47 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.-48-2188C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957446 | ||||||
| chr21:43957462
|
A | AGGGTTTC others(20): Show |
2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-2122_-48-2096d others(29): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957462 | |||||
| chr21:43957462
|
AGGGTTTC others(20): Show |
A | 1 | a0001c0001t0015g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-48-2122_-48-2096d others(29): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957462 | |||||
| chr21:43957480
|
G | GGGGGGTC others(73): Show |
1 | a0001c0001t0001g0184 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-48-2134_-48-2055d others(82): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957480 | |||||
| chr21:43957522
|
T | TCCCCTCC others(300): Show |
5 | a0001c0001t0007g0192a0001c0001t0007g0326a0001c0001t0007g0327others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-1845_-48-1844i others(309): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957522 | |||||
| chr21:43957522
|
T | TCCCCTCC others(300): Show |
5 | a0001c0001t0003g0085a0001c0001t0031g0195a0001c0001t0031g0196others(2): Show | 5 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-2094_-48-1788d others(309): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957522 | |||||
| chr21:43957560
|
C | T | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-2074C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957560 | ||||||
| chr21:43957660
|
CGGGGGTC others(20): Show |
C | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48-1947_-48-1921d others(29): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957660 | |||||
| chr21:43957769
|
G | A | 40 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0001g0297others(37): Show | 41 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.-48-1865G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957769 | ||||||
| chr21:43957769
|
G | GGGTTTCC others(47): Show |
6 | a0001c0001t0019g0069a0001c0001t0019g0323a0001c0001t0019g0330others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-1854_-48-1853i others(56): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957769 | |||||
| chr21:43957809
|
C | T | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48-1825C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957809 | ||||||
| chr21:43957850
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-48-1784A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957850 | ||||||
| chr21:43957939
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48-1695G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957939 | ||||||
| chr21:43958160
|
A | G | 191 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0152others(188): Show | 192 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.-48-1474A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958160 | ||||||
| chr21:43958206
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-1428G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958206 | ||||||
| chr21:43958356
|
T | A | 1 | a0001c0001t0040g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-48-1278T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958356 | ||||||
| chr21:43958381
|
G | A | 2 | a0001c0001t0004g0281a0001c0001t0004g0317 | 2 | HG02027.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-48-1253G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958381 | ||||||
| chr21:43958384
|
T | G | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-1250T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958384 | ||||||
| chr21:43958518
|
G | A | 2 | a0001c0002t0018g0114a0001c0002t0048g0298 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-48-1116G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958518 | ||||||
| chr21:43958639
|
TTGTGG | T | 47 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0001g0297others(44): Show | 48 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48-983_-48-979del others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43958639 | |||||
| chr21:43958671
|
A | G | 187 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0152others(184): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.-48-963A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958671 | ||||||
| chr21:43958750
|
A | AGT | 188 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0152others(185): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.-48-879_-48-878dup others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43958750 | |||||
| chr21:43958774
|
A | G | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48-860A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958774 | ||||||
| chr21:43958948
|
C | T | 5 | a0001c0001t0003g0119a0001c0001t0003g0123a0001c0001t0003g0124others(2): Show | 5 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-686C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958948 | ||||||
| chr21:43959082
|
T | TGGTGTGT others(22): Show |
49 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0001g0297others(46): Show | 50 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.-48-540_-48-539ins others(29): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959082 | |||||
| chr21:43959082
|
T | TGTGTGTG others(17): Show |
1 | a0001c0001t0004g0003 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-48-551_-48-550ins others(24): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959082 | |||||
| chr21:43959082
|
T | TGTGTGTG others(19): Show |
137 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0163others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-48-551_-48-550ins others(26): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959082 | |||||
| chr21:43959095
|
T | G | 1 | a0001c0001t0030g0331 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-48-539T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43959095 | ||||||
| chr21:43959229
|
TGTG | T | 42 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0001g0214others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.-48-401_-48-399del others(3): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959229 | |||||
| chr21:43959325
|
TTGTG | T | 35 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0001g0297others(32): Show | 36 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(33): Show |
intron_variant | MODIFIER | c.-48-300_-48-297del others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959325 | |||||
| chr21:43959339
|
C | T | 3 | a0001c0001t0003g0319a0001c0001t0032g0324a0001c0001t0032g0325 | 3 | HG01243.hp2 HG02818.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-48-295C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43959339 | ||||||
| chr21:43959474
|
TTGTA | T | 84 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0179others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-48-156_-48-153del others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959474 | |||||
| chr21:43959548
|
G | A | 2 | a0001c0001t0001g0297a0001c0001t0003g0319 | 2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-48-86G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43959548 | ||||||
| chr21:43959572
|
G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-62G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43959572 | ||||||
| chr21:43959622
|
C | T | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-48-12C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43959622 | ||||||
| chr21:43959914
|
G | A | 9 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(6): Show | 9 | HG01081.hp1 HG01261.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.178+55G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43959914 | ||||||
| chr21:43960092
|
G | T | 3 | a0001c0001t0006g0074a0001c0001t0006g0194a0001c0001t0027g0299 | 3 | HG03579.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178+233G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43960092 | ||||||
| chr21:43960198
|
C | T | 1 | a0001c0001t0004g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.178+339C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43960198 | ||||||
| chr21:43960249
|
C | T | 140 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0163others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.178+390C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43960249 | ||||||
| chr21:43960332
|
G | A | 110 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0179others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.178+473G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43960332 | ||||||
| chr21:43960763
|
A | G | 1 | a0001c0001t0002g0335 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.178+904A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43960763 | ||||||
| chr21:43961048
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.178+1189G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961048 | ||||||
| chr21:43961054
|
T | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0235 | 3 | NA19081.hp2 NA19082.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.178+1195T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961054 | ||||||
| chr21:43961141
|
T | TA | 14 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0034others(11): Show | 14 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.178+1297dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43961141 | |||||
| chr21:43961141
|
TA | T | 6 | a0001c0001t0001g0031a0001c0001t0001g0282a0001c0001t0001g0295others(3): Show | 6 | HG01496.hp2 HG02071.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+1297delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43961141 | |||||
| chr21:43961196
|
T | C | 4 | a0001c0001t0005g0322a0001c0001t0032g0324a0001c0001t0032g0325others(1): Show | 4 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+1337T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961196 | ||||||
| chr21:43961313
|
G | A | 4 | a0001c0001t0005g0322a0001c0001t0032g0324a0001c0001t0032g0325others(1): Show | 4 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+1454G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961313 | ||||||
| chr21:43961455
|
G | GGTGAGCA others(29): Show |
139 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0163others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.178+1601_178+1636d others(38): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43961455 | |||||
| chr21:43961496
|
A | G | 187 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0152others(184): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.178+1637A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961496 | ||||||
| chr21:43961524
|
C | T | 139 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0163others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.178+1665C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961524 | ||||||
| chr21:43961537
|
T | A | 1 | a0001c0001t0001g0146 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.178+1678T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961537 | ||||||
| chr21:43961579
|
T | C | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.178+1720T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961579 | ||||||
| chr21:43961585
|
C | CAT | 188 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0152others(185): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.178+1726_178+1727i others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961585 | ||||||
| chr21:43961601
|
C | T | 42 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0132others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(40): Show |
intron_variant | MODIFIER | c.178+1742C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961601 | ||||||
| chr21:43961605
|
C | CATACACT others(65): Show |
6 | a0001c0001t0019g0069a0001c0001t0019g0323a0001c0001t0019g0330others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+1786_178+1787i others(74): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43961605 | |||||
| chr21:43961631
|
G | A | 1 | a0001c0001t0012g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178+1772G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961631 | ||||||
| chr21:43961637
|
C | T | 1 | a0001c0001t0026g0059 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.178+1778C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961637 | ||||||
| chr21:43961646
|
G | A | 236 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0048others(233): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.178+1787G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961646 | ||||||
| chr21:43961832
|
G | C | 189 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0152others(186): Show | 190 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.178+1973G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961832 | ||||||
| chr21:43961836
|
G | A | 1 | a0001c0001t0015g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.178+1977G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961836 | ||||||
| chr21:43962003
|
C | CT | 15 | a0001c0001t0001g0034a0001c0001t0003g0130a0001c0001t0005g0322others(12): Show | 15 | HG01243.hp2 HG01433.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+2159dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43962003 | |||||
| chr21:43962003
|
C | CTT | 44 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0002g0132others(41): Show | 45 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(42): Show |
intron_variant | MODIFIER | c.178+2158_178+2159d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43962003 | |||||
| chr21:43962024
|
T | G | 1 | a0001c0001t0006g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.178+2165T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962024 | ||||||
| chr21:43962039
|
T | C | 1 | a0003c0007t0001g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.178+2180T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962039 | ||||||
| chr21:43962063
|
C | T | 139 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0163others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.178+2204C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962063 | ||||||
| chr21:43962066
|
T | C | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.178+2207T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962066 | ||||||
| chr21:43962086
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.178+2227T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962086 | ||||||
| chr21:43962125
|
C | T | 1 | a0001c0001t0004g0278 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.178+2266C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962125 | ||||||
| chr21:43962146
|
A | G | 1 | a0001c0001t0041g0091 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.178+2287A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962146 | ||||||
| chr21:43962167
|
A | T | 1 | a0001c0001t0001g0182 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.178+2308A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962167 | ||||||
| chr21:43962217
|
T | G | 1 | a0001c0001t0016g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.178+2358T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962217 | ||||||
| chr21:43962218
|
G | T | 1 | a0001c0001t0016g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.178+2359G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962218 | ||||||
| chr21:43962221
|
T | C | 1 | a0001c0001t0016g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.178+2362T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962221 | ||||||
| chr21:43962225
|
A | G | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+2366A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962225 | ||||||
| chr21:43962238
|
G | A | 138 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0163others(135): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.178+2379G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962238 | ||||||
| chr21:43962254
|
G | A | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.178+2395G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962254 | ||||||
| chr21:43962291
|
C | T | 113 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0168others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.178+2432C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962291 | ||||||
| chr21:43962369
|
A | G | 6 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+2510A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962369 | ||||||
| chr21:43962388
|
T | A | 2 | a0001c0001t0028g0242a0001c0001t0063g0273 | 2 | NA18962.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.178+2529T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962388 | ||||||
| chr21:43962892
|
T | TGACCCAC others(10): Show |
112 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0168others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.178+3034_178+3050d others(19): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43962892 | |||||
| chr21:43962980
|
A | G | 72 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0164others(69): Show | 73 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.178+3121A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962980 | ||||||
| chr21:43963363
|
C | T | 1 | a0001c0001t0006g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.178+3504C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963363 | ||||||
| chr21:43963447
|
C | T | 1 | a0001c0001t0029g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.178+3588C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963447 | ||||||
| chr21:43963448
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.178+3589G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963448 | ||||||
| chr21:43963481
|
A | G | 77 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0164others(74): Show | 78 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.178+3622A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963481 | ||||||
| chr21:43963555
|
T | C | 76 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0164others(73): Show | 77 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.178+3696T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963555 | ||||||
| chr21:43963637
|
G | A | 1 | a0001c0001t0002g0335 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.178+3778G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963637 | ||||||
| chr21:43963707
|
C | CA | 11 | a0001c0001t0001g0034a0001c0001t0001g0173a0001c0001t0001g0174others(8): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.178+3871dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43963707 | |||||
| chr21:43963707
|
CA | C | 125 | a0001c0001t0001g0152a0001c0001t0001g0162a0001c0001t0001g0163others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.178+3871delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43963707 | |||||
| chr21:43963707
|
CAA | C | 6 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(3): Show | 6 | HG01109.hp1 HG02559.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+3870_178+3871d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43963707 | |||||
| chr21:43963739
|
A | T | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+3880A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963739 | ||||||
| chr21:43963763
|
A | G | 5 | a0001c0001t0007g0192a0001c0001t0007g0326a0001c0001t0007g0327others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+3904A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963763 | ||||||
| chr21:43963800
|
G | A | 5 | a0001c0001t0005g0322a0001c0001t0032g0324a0001c0001t0032g0325others(2): Show | 5 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+3941G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963800 | ||||||
| chr21:43963833
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.178+3974G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963833 | ||||||
| chr21:43963833
|
G | C | 1 | a0001c0001t0072g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.178+3974G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963833 | ||||||
| chr21:43963955
|
A | G | 1 | a0001c0001t0059g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.179-3991A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963955 | ||||||
| chr21:43964022
|
A | C | 77 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0164others(74): Show | 78 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.179-3924A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964022 | ||||||
| chr21:43964318
|
G | A | 2 | a0001c0001t0044g0093a0001c0001t0045g0104 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.179-3628G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964318 | ||||||
| chr21:43964559
|
C | A | 1 | a0001c0001t0061g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.179-3387C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964559 | ||||||
| chr21:43964598
|
C | G | 1 | a0001c0001t0046g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-3348C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964598 | ||||||
| chr21:43964651
|
G | A | 2 | a0001c0001t0044g0093a0001c0001t0045g0104 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.179-3295G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964651 | ||||||
| chr21:43964938
|
T | C | 2 | a0001c0002t0018g0114a0001c0002t0048g0298 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.179-3008T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964938 | ||||||
| chr21:43964961
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0076g0279 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.179-2985C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964961 | ||||||
| chr21:43965223
|
C | T | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-2723C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965223 | ||||||
| chr21:43965253
|
C | T | 2 | a0001c0001t0041g0091a0001c0001t0057g0208 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.179-2693C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965253 | ||||||
| chr21:43965259
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.179-2687T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965259 | ||||||
| chr21:43965396
|
G | A | 7 | a0001c0001t0006g0205a0001c0001t0012g0076a0001c0001t0012g0099others(4): Show | 7 | HG01891.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-2550G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965396 | ||||||
| chr21:43965402
|
A | T | 2 | a0001c0001t0002g0050a0001c0001t0054g0022 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.179-2544A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965402 | ||||||
| chr21:43965406
|
G | A | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-2540G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965406 | ||||||
| chr21:43965604
|
G | GT | 13 | a0001c0001t0001g0252a0001c0001t0005g0322a0001c0001t0012g0070others(10): Show | 13 | HG01243.hp2 HG02109.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-2334dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43965604 | |||||
| chr21:43965604
|
G | GTT | 56 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0295others(53): Show | 57 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.179-2335_179-2334d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43965604 | |||||
| chr21:43965613
|
G | T | 18 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0005g0322others(15): Show | 18 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.179-2333G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965613 | ||||||
| chr21:43965777
|
A | T | 2 | a0001c0001t0001g0169a0001c0001t0066g0027 | 2 | HG01123.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.179-2169A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965777 | ||||||
| chr21:43965777
|
AT | A | 75 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0295others(72): Show | 76 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.179-2161delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43965777 | |||||
| chr21:43965790
|
T | G | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-2156T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965790 | ||||||
| chr21:43965806
|
T | G | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.179-2140T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965806 | ||||||
| chr21:43965898
|
C | T | 18 | a0001c0001t0001g0334a0001c0001t0002g0120a0001c0001t0002g0149others(15): Show | 18 | HG00558.hp2 HG01943.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.179-2048C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965898 | ||||||
| chr21:43965924
|
T | C | 5 | a0001c0001t0001g0162a0001c0001t0001g0221a0001c0001t0001g0251others(2): Show | 5 | HG02015.hp2 HG02080.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-2022T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965924 | ||||||
| chr21:43966026
|
A | G | 66 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0295others(63): Show | 67 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.179-1920A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966026 | ||||||
| chr21:43966130
|
A | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.179-1816A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966130 | ||||||
| chr21:43966152
|
A | G | 209 | a0001c0001t0001g0048a0001c0001t0001g0150a0001c0001t0001g0152others(206): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.179-1794A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966152 | ||||||
| chr21:43966200
|
T | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.179-1746T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966200 | ||||||
| chr21:43966360
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.179-1586G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966360 | ||||||
| chr21:43966370
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0001g0232a0001c0001t0001g0283 | 3 | HG02080.hp1 NA18952.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.179-1576C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966370 | ||||||
| chr21:43966420
|
G | A | 2 | a0001c0001t0029g0083a0001c0001t0029g0144 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.179-1526G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966420 | ||||||
| chr21:43966453
|
T | C | 1 | a0001c0001t0040g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.179-1493T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966453 | ||||||
| chr21:43966588
|
C | T | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-1358C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966588 | ||||||
| chr21:43966631
|
G | A | 27 | a0001c0001t0003g0085a0001c0001t0007g0192a0001c0001t0007g0326others(24): Show | 27 | HG01081.hp1 HG01109.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-1315G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966631 | ||||||
| chr21:43966678
|
T | C | 75 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0295others(72): Show | 76 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.179-1268T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966678 | ||||||
| chr21:43966803
|
G | A | 2 | a0001c0002t0018g0114a0001c0002t0048g0298 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.179-1143G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966803 | ||||||
| chr21:43966857
|
G | C | 1 | a0001c0001t0063g0273 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.179-1089G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966857 | ||||||
| chr21:43966864
|
TTCCCGGA others(11): Show |
T | 1 | a0001c0001t0002g0338 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.179-1081_179-1064d others(20): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966864 | ||||||
| chr21:43966902
|
G | C | 1 | a0001c0001t0063g0273 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.179-1044G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966902 | ||||||
| chr21:43966903
|
C | G | 1 | a0001c0001t0063g0273 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.179-1043C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966903 | ||||||
| chr21:43966950
|
T | C | 325 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0026others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.179-996T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966950 | ||||||
| chr21:43967117
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.179-829C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967117 | ||||||
| chr21:43967127
|
T | C | 196 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0163others(193): Show | 197 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.179-819T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967127 | ||||||
| chr21:43967228
|
A | G | 103 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0295others(100): Show | 104 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.179-718A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967228 | ||||||
| chr21:43967260
|
G | A | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.179-686G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967260 | ||||||
| chr21:43967325
|
C | A | 2 | a0001c0002t0018g0114a0001c0002t0048g0298 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.179-621C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967325 | ||||||
| chr21:43967362
|
C | T | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.179-584C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967362 | ||||||
| chr21:43967407
|
T | G | 1 | a0001c0001t0014g0266 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.179-539T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967407 | ||||||
| chr21:43967440
|
T | A | 7 | a0001c0001t0005g0322a0001c0001t0032g0324a0001c0001t0032g0325others(4): Show | 7 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-506T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967440 | ||||||
| chr21:43967537
|
T | C | 3 | a0001c0001t0030g0073a0001c0001t0030g0331a0001c0001t0050g0024 | 3 | HG02257.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.179-409T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967537 | ||||||
| chr21:43967675
|
G | A | 9 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(6): Show | 9 | HG01081.hp1 HG01261.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-271G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967675 | ||||||
| chr21:43967710
|
G | A | 2 | a0001c0001t0004g0286a0001c0001t0004g0314 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.179-236G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967710 | ||||||
| chr21:43967765
|
C | A | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0276 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.179-181C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967765 | ||||||
| chr21:43967784
|
A | G | 2 | a0001c0001t0044g0093a0001c0001t0045g0104 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.179-162A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967784 | ||||||
| chr21:43967790
|
A | G | 1 | a0001c0001t0081g0136 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.179-156A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967790 | ||||||
| chr21:43968122
|
G | A | 1 | a0001c0001t0006g0241 | 1 | HG01099.hp2 | splice_region_variant&intron_variant | LOW | c.348+7G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968122 | ||||||
| chr21:43968170
|
C | T | 1 | a0001c0001t0017g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.348+55C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968170 | ||||||
| chr21:43968198
|
CG | C | 31 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0295others(28): Show | 31 | HG00323.hp2 HG01175.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.348+87delG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr21 | 43968198 | |||||
| chr21:43968259
|
C | CG | 5 | a0001c0001t0001g0248a0001c0001t0002g0023a0001c0001t0004g0311others(2): Show | 5 | HG00544.hp1 HG01099.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+148dupG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr21 | 43968259 | |||||
| chr21:43968330
|
C | T | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.348+215C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968330 | ||||||
| chr21:43968450
|
G | A | 1 | a0001c0001t0003g0128 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.348+335G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968450 | ||||||
| chr21:43968470
|
G | A | 1 | a0001c0001t0022g0051 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.348+355G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968470 | ||||||
| chr21:43968472
|
G | A | 111 | a0001c0001t0001g0048a0001c0001t0001g0152a0001c0001t0001g0163others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.348+357G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968472 | ||||||
| chr21:43968474
|
G | A | 46 | a0001c0001t0001g0222a0001c0001t0001g0233a0001c0001t0001g0245others(43): Show | 47 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.348+359G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968474 | ||||||
| chr21:43968763
|
A | G | 207 | a0001c0001t0001g0048a0001c0001t0001g0142a0001c0001t0001g0150others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.349-355A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968763 | ||||||
| chr21:43968782
|
C | G | 1 | a0001c0001t0037g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.349-336C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968782 | ||||||
| chr21:43968878
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0004g0240 | 2 | HG00140.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.349-240G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968878 | ||||||
| chr21:43969324
|
C | A | 2 | a0001c0002t0018g0114a0001c0002t0048g0298 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.510+45C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969324 | ||||||
| chr21:43969380
|
A | G | 44 | a0001c0001t0001g0295a0001c0001t0002g0014a0001c0001t0002g0015others(41): Show | 44 | HG00323.hp2 HG01081.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.510+101A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969380 | ||||||
| chr21:43969467
|
T | C | 99 | a0001c0001t0001g0295a0001c0001t0002g0132a0001c0001t0002g0171others(96): Show | 100 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.510+188T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969467 | ||||||
| chr21:43969526
|
A | G | 1 | a0001c0001t0002g0338 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.510+247A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969526 | ||||||
| chr21:43969546
|
C | T | 2 | a0001c0001t0032g0324a0001c0001t0032g0325 | 2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.510+267C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969546 | ||||||
| chr21:43969569
|
G | T | 1 | a0001c0001t0001g0274 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.510+290G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969569 | ||||||
| chr21:43969671
|
C | T | 186 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0168others(183): Show | 187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.510+392C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969671 | ||||||
| chr21:43969696
|
T | G | 2 | a0001c0002t0018g0114a0001c0002t0048g0298 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.510+417T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969696 | ||||||
| chr21:43969696
|
T | TTG | 11 | a0001c0001t0001g0168a0001c0001t0012g0070a0001c0001t0016g0071others(8): Show | 11 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+433_510+434dup others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr21 | 43969696 | |||||
| chr21:43969745
|
T | C | 3 | a0001c0001t0017g0098a0001c0001t0029g0083a0001c0001t0029g0144 | 3 | HG02486.hp2 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.510+466T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969745 | ||||||
| chr21:43969908
|
A | G | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+629A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969908 | ||||||
| chr21:43969997
|
C | G | 1 | a0001c0001t0019g0330 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.511-656C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969997 | ||||||
| chr21:43970012
|
C | CT | 69 | a0001c0001t0002g0132a0001c0001t0002g0171a0001c0001t0003g0002others(66): Show | 70 | HG00544.hp2 HG00597.hp2 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.511-632dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr21 | 43970012 | |||||
| chr21:43970052
|
A | G | 1 | a0001c0001t0032g0325 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.511-601A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970052 | ||||||
| chr21:43970071
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.511-582T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970071 | ||||||
| chr21:43970115
|
TCTC | T | 8 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(5): Show | 8 | HG01109.hp1 HG02559.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-534_511-532del others(3): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr21 | 43970115 | |||||
| chr21:43970155
|
T | A | 1 | a0001c0001t0019g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.511-498T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970155 | ||||||
| chr21:43970156
|
C | A | 1 | a0001c0001t0019g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.511-497C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970156 | ||||||
| chr21:43970157
|
A | G | 1 | a0001c0001t0019g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.511-496A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970157 | ||||||
| chr21:43970164
|
C | T | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.511-489C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970164 | ||||||
| chr21:43970197
|
G | A | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.511-456G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970197 | ||||||
| chr21:43970298
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.511-355G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970298 | ||||||
| chr21:43970400
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.511-253G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970400 | ||||||
| chr21:43970474
|
CTG | C | 59 | a0001c0001t0001g0295a0001c0001t0002g0132a0001c0001t0002g0171others(56): Show | 60 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.511-176_511-175del others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr21 | 43970474 | |||||
| chr21:43970529
|
C | T | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.511-124C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970529 | ||||||
| chr21:43970621
|
G | C | 1 | a0001c0001t0002g0238 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.511-32G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970621 | ||||||
| chr21:43970825
|
G | A | 4 | a0001c0001t0005g0086a0001c0001t0005g0088a0001c0001t0005g0089others(1): Show | 4 | HG02602.hp2 HG02683.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+19G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43970825 | ||||||
| chr21:43970856
|
T | C | 24 | a0001c0001t0001g0295a0001c0001t0008g0039a0001c0001t0008g0042others(21): Show | 24 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.664+50T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43970856 | ||||||
| chr21:43970868
|
T | TA | 83 | a0001c0001t0001g0255a0001c0001t0001g0295a0001c0001t0002g0132others(80): Show | 84 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.664+76dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr21 | 43970868 | |||||
| chr21:43970883
|
T | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0169 | 2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.664+77T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43970883 | ||||||
| chr21:43970961
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.664+155C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43970961 | ||||||
| chr21:43971087
|
C | G | 1 | a0001c0001t0004g0004 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.664+281C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971087 | ||||||
| chr21:43971148
|
G | A | 2 | a0001c0002t0018g0114a0001c0002t0048g0298 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.665-240G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971148 | ||||||
| chr21:43971164
|
A | G | 6 | a0001c0001t0012g0076a0001c0001t0017g0098a0001c0001t0029g0083others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-224A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971164 | ||||||
| chr21:43971175
|
C | G | 5 | a0001c0001t0003g0135a0001c0001t0032g0324a0001c0001t0032g0325others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-213C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971175 | ||||||
| chr21:43971258
|
G | A | 45 | a0001c0001t0001g0295a0001c0001t0002g0132a0001c0001t0002g0171others(42): Show | 45 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.665-130G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971258 | ||||||
| chr21:43971374
|
G | A | 31 | a0001c0001t0002g0132a0001c0001t0002g0171a0001c0001t0003g0080others(28): Show | 31 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.665-14G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971374 | ||||||
| chr21:43971602
|
G | C | 5 | a0001c0001t0036g0094a0001c0001t0037g0304a0001c0001t0038g0109others(2): Show | 5 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.767+112G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971602 | ||||||
| chr21:43971670
|
A | G | 7 | a0001c0001t0009g0030a0001c0001t0009g0226a0001c0001t0009g0227others(4): Show | 7 | HG01358.hp2 HG01943.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.767+180A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971670 | ||||||
| chr21:43971721
|
G | A | 3 | a0001c0001t0036g0094a0001c0001t0038g0109a0001c0001t0039g0102 | 3 | HG02559.hp1 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.767+231G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971721 | ||||||
| chr21:43971756
|
T | C | 1 | a0001c0001t0006g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.767+266T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971756 | ||||||
| chr21:43971762
|
T | G | 5 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(2): Show | 5 | HG02965.hp2 NA18522.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.767+272T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971762 | ||||||
| chr21:43971871
|
T | C | 238 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0054others(235): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.767+381T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971871 | ||||||
| chr21:43971917
|
G | A | 33 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(30): Show | 33 | HG01167.hp2 HG01884.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.767+427G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971917 | ||||||
| chr21:43971931
|
G | A | 1 | a0001c0001t0026g0191 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.767+441G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971931 | ||||||
| chr21:43971946
|
C | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | HG01167.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.767+456C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971946 | ||||||
| chr21:43971954
|
A | C | 3 | a0001c0001t0015g0116a0001c0001t0032g0324a0001c0001t0032g0325 | 3 | HG01243.hp2 HG01261.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.767+464A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971954 | ||||||
| chr21:43971964
|
G | A | 4 | a0001c0001t0002g0078a0001c0001t0005g0322a0001c0001t0017g0077others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.767+474G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971964 | ||||||
| chr21:43972135
|
A | C | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.767+645A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972135 | ||||||
| chr21:43972147
|
A | AT | 130 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0152others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.767+668dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43972147 | |||||
| chr21:43972183
|
C | T | 1 | a0001c0001t0040g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.767+693C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972183 | ||||||
| chr21:43972231
|
G | A | 1 | a0001c0001t0063g0273 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.767+741G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972231 | ||||||
| chr21:43972251
|
T | A | 1 | a0001c0001t0066g0027 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.767+761T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972251 | ||||||
| chr21:43972397
|
C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.767+907C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972397 | ||||||
| chr21:43972767
|
C | A | 1 | a0001c0001t0002g0333 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.767+1277C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972767 | ||||||
| chr21:43972965
|
A | G | 143 | a0001c0001t0001g0048a0001c0001t0001g0152a0001c0001t0001g0163others(140): Show | 144 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.767+1475A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972965 | ||||||
| chr21:43972972
|
G | A | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.767+1482G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972972 | ||||||
| chr21:43973042
|
G | A | 98 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0200others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+1552G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973042 | ||||||
| chr21:43973199
|
G | C | 209 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0200others(206): Show | 211 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.767+1709G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973199 | ||||||
| chr21:43973242
|
G | A | 2 | a0001c0001t0029g0083a0001c0001t0029g0144 | 2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.767+1752G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973242 | ||||||
| chr21:43973296
|
C | T | 20 | a0001c0001t0008g0039a0001c0001t0008g0042a0001c0001t0008g0043others(17): Show | 20 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.767+1806C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973296 | ||||||
| chr21:43973421
|
C | T | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.767+1931C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973421 | ||||||
| chr21:43973520
|
C | T | 1 | a0001c0001t0020g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.767+2030C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973520 | ||||||
| chr21:43973568
|
G | A | 118 | a0001c0001t0001g0026a0001c0001t0001g0152a0001c0001t0001g0163others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.767+2078G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973568 | ||||||
| chr21:43973602
|
T | C | 9 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.767+2112T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973602 | ||||||
| chr21:43973640
|
G | A | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.767+2150G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973640 | ||||||
| chr21:43973648
|
C | A | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.767+2158C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973648 | ||||||
| chr21:43973651
|
G | C | 4 | a0001c0001t0006g0074a0001c0001t0006g0194a0001c0001t0027g0067others(1): Show | 4 | HG03041.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.767+2161G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973651 | ||||||
| chr21:43973661
|
G | A | 164 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0200others(161): Show | 165 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.767+2171G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973661 | ||||||
| chr21:43973714
|
G | A | 3 | a0001c0001t0031g0195a0001c0001t0031g0196a0001c0001t0062g0313 | 3 | HG01257.hp1 HG01258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.767+2224G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973714 | ||||||
| chr21:43973801
|
G | A | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.767+2311G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973801 | ||||||
| chr21:43973869
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.767+2379C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973869 | ||||||
| chr21:43973944
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.767+2454A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973944 | ||||||
| chr21:43974114
|
A | G | 6 | a0001c0001t0029g0083a0001c0001t0029g0144a0001c0001t0045g0104others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.767+2624A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974114 | ||||||
| chr21:43974144
|
C | A | 1 | a0001c0001t0004g0047 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.767+2654C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974144 | ||||||
| chr21:43974144
|
C | G | 42 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0168others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.767+2654C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974144 | ||||||
| chr21:43974144
|
C | T | 28 | a0001c0001t0005g0082a0001c0001t0005g0086a0001c0001t0005g0088others(25): Show | 29 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.767+2654C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974144 | ||||||
| chr21:43974167
|
A | G | 1 | a0001c0001t0007g0154 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.767+2677A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974167 | ||||||
| chr21:43974218
|
TTATC | T | 98 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0200others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+2732_767+2735d others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43974218 | |||||
| chr21:43974339
|
G | A | 7 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(4): Show | 7 | HG01109.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.767+2849G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974339 | ||||||
| chr21:43974417
|
TGTG | T | 20 | a0001c0001t0008g0039a0001c0001t0008g0042a0001c0001t0008g0043others(17): Show | 20 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.767+2931_767+2933d others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43974417 | |||||
| chr21:43974489
|
G | A | 1 | a0001c0001t0050g0024 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.767+2999G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974489 | ||||||
| chr21:43974547
|
ATGTGTGT others(4): Show |
A | 10 | a0001c0001t0019g0069a0001c0001t0019g0323a0001c0001t0019g0330others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.767+3065_767+3075d others(13): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43974547 | |||||
| chr21:43974669
|
G | T | 5 | a0001c0001t0024g0106a0001c0001t0024g0107a0001c0001t0034g0105others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.767+3179G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974669 | ||||||
| chr21:43974836
|
C | A | 18 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0113others(15): Show | 18 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.768-3210C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974836 | ||||||
| chr21:43974968
|
G | A | 3 | a0001c0001t0029g0083a0001c0001t0029g0144a0001c0001t0045g0104 | 3 | HG02486.hp2 HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.768-3078G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974968 | ||||||
| chr21:43975236
|
TTGG | T | 89 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0200others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.768-2807_768-2805d others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43975236 | |||||
| chr21:43975239
|
G | T | 7 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(4): Show | 7 | HG01109.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.768-2807G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975239 | ||||||
| chr21:43975277
|
C | T | 6 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(3): Show | 6 | HG02293.hp1 HG02300.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.768-2769C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975277 | ||||||
| chr21:43975309
|
A | AGTGTGCT others(30): Show |
1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.768-2726_768-2690d others(39): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43975309 | |||||
| chr21:43975314
|
G | T | 1 | a0001c0001t0001g0248 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.768-2732G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975314 | ||||||
| chr21:43975340
|
T | C | 46 | a0001c0001t0003g0002a0001c0001t0003g0080a0001c0001t0003g0085others(43): Show | 47 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.768-2706T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975340 | ||||||
| chr21:43975357
|
ATG | A | 5 | a0001c0001t0024g0106a0001c0001t0024g0107a0001c0001t0034g0105others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-2682_768-2681d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43975357 | |||||
| chr21:43975434
|
G | A | 2 | a0001c0001t0044g0093a0001c0001t0052g0220 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.768-2612G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975434 | ||||||
| chr21:43975584
|
G | A | 5 | a0001c0001t0024g0106a0001c0001t0024g0107a0001c0001t0034g0105others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-2462G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975584 | ||||||
| chr21:43975631
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.768-2415G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975631 | ||||||
| chr21:43975643
|
G | A | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.768-2403G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975643 | ||||||
| chr21:43975723
|
G | T | 8 | a0001c0001t0024g0106a0001c0001t0024g0107a0001c0001t0034g0105others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.768-2323G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975723 | ||||||
| chr21:43975728
|
T | G | 1 | a0001c0001t0016g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.768-2318T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975728 | ||||||
| chr21:43975772
|
C | A | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.768-2274C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975772 | ||||||
| chr21:43975807
|
C | T | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.768-2239C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975807 | ||||||
| chr21:43975918
|
A | G | 168 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0168others(165): Show | 169 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.768-2128A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975918 | ||||||
| chr21:43975921
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.768-2125C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975921 | ||||||
| chr21:43975943
|
G | A | 1 | a0001c0001t0003g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.768-2103G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975943 | ||||||
| chr21:43975960
|
G | A | 1 | a0001c0001t0009g0230 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.768-2086G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975960 | ||||||
| chr21:43975982
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.768-2064T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975982 | ||||||
| chr21:43975985
|
C | CT | 55 | a0001c0001t0001g0221a0001c0001t0001g0243a0001c0001t0002g0016others(52): Show | 56 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.768-2047dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43975985 | |||||
| chr21:43975985
|
C | CTT | 94 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0168others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.768-2048_768-2047d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43975985 | |||||
| chr21:43976040
|
A | G | 71 | a0001c0001t0003g0002a0001c0001t0003g0080a0001c0001t0003g0085others(68): Show | 72 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.768-2006A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976040 | ||||||
| chr21:43976072
|
TA | T | 4 | a0001c0001t0012g0070a0001c0001t0016g0071a0001c0001t0016g0072others(1): Show | 4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.768-1973delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976072 | ||||||
| chr21:43976073
|
A | T | 47 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0003g0002others(44): Show | 48 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.768-1973A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976073 | ||||||
| chr21:43976073
|
AT | A | 22 | a0001c0001t0008g0039a0001c0001t0008g0042a0001c0001t0008g0043others(19): Show | 22 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.768-1961delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43976073 | |||||
| chr21:43976079
|
T | A | 9 | a0001c0001t0002g0056a0001c0001t0002g0060a0001c0001t0002g0132others(6): Show | 9 | HG02135.hp1 HG02293.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.768-1967T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976079 | ||||||
| chr21:43976091
|
G | A | 97 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0168others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.768-1955G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976091 | ||||||
| chr21:43976153
|
C | T | 2 | a0001c0001t0004g0079a0001c0001t0004g0126 | 2 | HG01175.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.768-1893C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976153 | ||||||
| chr21:43976154
|
G | A | 1 | a0001c0001t0004g0010 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.768-1892G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976154 | ||||||
| chr21:43976487
|
A | G | 1 | a0001c0001t0004g0240 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.768-1559A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976487 | ||||||
| chr21:43976554
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.768-1492C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976554 | ||||||
| chr21:43976576
|
T | G | 40 | a0001c0001t0003g0002a0001c0001t0003g0080a0001c0001t0003g0085others(37): Show | 41 | HG00544.hp2 HG00597.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.768-1470T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976576 | ||||||
| chr21:43976597
|
G | A | 40 | a0001c0001t0003g0002a0001c0001t0003g0080a0001c0001t0003g0085others(37): Show | 41 | HG00544.hp2 HG00597.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.768-1449G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976597 | ||||||
| chr21:43976673
|
A | G | 3 | a0001c0001t0049g0320a0001c0002t0018g0114a0001c0002t0048g0298 | 3 | HG02109.hp1 HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.768-1373A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976673 | ||||||
| chr21:43976742
|
G | C | 1 | a0001c0001t0070g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.768-1304G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976742 | ||||||
| chr21:43976762
|
G | A | 40 | a0001c0001t0003g0002a0001c0001t0003g0080a0001c0001t0003g0085others(37): Show | 41 | HG00544.hp2 HG00597.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.768-1284G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976762 | ||||||
| chr21:43976852
|
C | T | 20 | a0001c0001t0008g0039a0001c0001t0008g0042a0001c0001t0008g0043others(17): Show | 20 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.768-1194C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976852 | ||||||
| chr21:43976992
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.768-1054G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976992 | ||||||
| chr21:43977084
|
C | A | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.768-962C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977084 | ||||||
| chr21:43977087
|
A | G | 99 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0200others(96): Show | 99 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.768-959A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977087 | ||||||
| chr21:43977129
|
G | C | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.768-917G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977129 | ||||||
| chr21:43977137
|
C | T | 2 | a0001c0001t0044g0093a0001c0001t0052g0220 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.768-909C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977137 | ||||||
| chr21:43977148
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.768-898C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977148 | ||||||
| chr21:43977174
|
A | C | 1 | a0001c0001t0002g0333 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.768-872A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977174 | ||||||
| chr21:43977388
|
G | A | 1 | a0001c0001t0004g0047 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.768-658G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977388 | ||||||
| chr21:43977454
|
C | G | 46 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0135others(43): Show | 47 | HG00323.hp2 HG01243.hp2 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.768-592C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977454 | ||||||
| chr21:43977455
|
C | G | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.768-591C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977455 | ||||||
| chr21:43977516
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.768-530T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977516 | ||||||
| chr21:43977527
|
CTG | C | 4 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(1): Show | 4 | HG01261.hp2 HG01496.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-515_768-514del others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43977527 | |||||
| chr21:43977585
|
T | C | 7 | a0001c0001t0020g0064a0001c0001t0020g0065a0001c0001t0020g0066others(4): Show | 7 | HG01109.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.768-461T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977585 | ||||||
| chr21:43977659
|
C | T | 96 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0200others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.768-387C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977659 | ||||||
| chr21:43977729
|
GA | G | 10 | a0001c0001t0003g0080a0001c0001t0003g0121a0001c0001t0003g0125others(7): Show | 10 | NA18941.hp2 NA18966.hp1 NA18974.hp2 others(7): Show |
intron_variant | MODIFIER | c.768-309delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43977729 | |||||
| chr21:43977885
|
C | CA | 33 | a0001c0001t0001g0113a0001c0001t0001g0148a0001c0001t0001g0197others(30): Show | 33 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.768-147dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43977885 | |||||
| chr21:43977885
|
C | CAA | 6 | a0001c0001t0024g0106a0001c0001t0024g0107a0001c0001t0034g0105others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.768-148_768-147dup others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43977885 | |||||
| chr21:43977918
|
G | A | 2 | a0001c0001t0044g0093a0001c0001t0052g0220 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.768-128G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977918 | ||||||
| chr21:43977980
|
G | A | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.768-66G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977980 | ||||||
| chr21:43978147
|
G | A | 1 | a0001c0001t0065g0020 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.843+26G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978147 | ||||||
| chr21:43978204
|
G | A | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.843+83G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978204 | ||||||
| chr21:43978279
|
G | GTTGTT | 51 | a0001c0001t0003g0002a0001c0001t0003g0080a0001c0001t0003g0085others(48): Show | 52 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.843+171_843+175dup others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43978279 | |||||
| chr21:43978325
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0010g0095others(1): Show | 4 | HG00639.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+204C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978325 | ||||||
| chr21:43978599
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.843+478A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978599 | ||||||
| chr21:43978607
|
T | G | 166 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0200others(163): Show | 167 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.843+486T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978607 | ||||||
| chr21:43978775
|
C | T | 166 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0200others(163): Show | 167 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.843+654C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978775 | ||||||
| chr21:43978843
|
C | T | 2 | a0001c0001t0044g0093a0001c0001t0052g0220 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.843+722C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978843 | ||||||
| chr21:43978844
|
G | A | 1 | a0001c0001t0008g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.843+723G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978844 | ||||||
| chr21:43978918
|
C | T | 42 | a0001c0001t0003g0002a0001c0001t0003g0080a0001c0001t0003g0085others(39): Show | 43 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.843+797C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978918 | ||||||
| chr21:43978928
|
G | A | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.843+807G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978928 | ||||||
| chr21:43978935
|
A | T | 3 | a0001c0001t0031g0195a0001c0001t0031g0196a0001c0001t0062g0313 | 3 | HG01257.hp1 HG01258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.843+814A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978935 | ||||||
| chr21:43978972
|
C | A | 91 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(88): Show | 91 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.843+851C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978972 | ||||||
| chr21:43979298
|
C | CA | 60 | a0001c0001t0001g0163a0001c0001t0003g0002a0001c0001t0003g0080others(57): Show | 61 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.843+1195dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43979298 | |||||
| chr21:43979298
|
C | CAA | 105 | a0001c0001t0001g0152a0001c0001t0001g0200a0001c0001t0001g0243others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.843+1194_843+1195d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43979298 | |||||
| chr21:43979298
|
C | CAAA | 10 | a0001c0001t0002g0014a0001c0001t0002g0023a0001c0001t0002g0049others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.843+1193_843+1195d others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43979298 | |||||
| chr21:43979321
|
G | GA | 6 | a0001c0001t0001g0275a0001c0001t0024g0106a0001c0001t0024g0107others(3): Show | 6 | HG02055.hp2 HG02074.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+1209dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43979321 | |||||
| chr21:43979335
|
GA | G | 99 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0200others(96): Show | 99 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.843+1225delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43979335 | |||||
| chr21:43979579
|
G | A | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.844-1410G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43979579 | ||||||
| chr21:43979690
|
T | C | 23 | a0001c0001t0008g0039a0001c0001t0008g0042a0001c0001t0008g0043others(20): Show | 23 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-1299T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43979690 | ||||||
| chr21:43979843
|
C | T | 5 | a0001c0001t0024g0106a0001c0001t0024g0107a0001c0001t0034g0105others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-1146C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43979843 | ||||||
| chr21:43979909
|
G | T | 5 | a0001c0001t0001g0222a0001c0001t0001g0233a0001c0001t0001g0245others(2): Show | 5 | HG01261.hp1 HG01346.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-1080G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43979909 | ||||||
| chr21:43980034
|
G | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG01070.hp2 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.844-955G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980034 | ||||||
| chr21:43980209
|
G | A | 6 | a0001c0001t0019g0069a0001c0001t0019g0323a0001c0001t0019g0330others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-780G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980209 | ||||||
| chr21:43980221
|
A | G | 1 | a0001c0001t0008g0159 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.844-768A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980221 | ||||||
| chr21:43980275
|
C | CA | 32 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0058others(29): Show | 32 | HG00099.hp2 HG00423.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.844-698dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43980275 | |||||
| chr21:43980286
|
A | C | 13 | a0001c0001t0001g0048a0001c0001t0005g0082a0001c0001t0005g0086others(10): Show | 14 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.844-703A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980286 | ||||||
| chr21:43980287
|
A | C | 2 | a0001c0001t0036g0094a0001c0001t0037g0304 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.844-702A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980287 | ||||||
| chr21:43980289
|
AAAC | A | 6 | a0001c0001t0003g0002a0001c0001t0003g0135a0001c0001t0003g0139others(3): Show | 7 | HG02258.hp2 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-697_844-695del others(3): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43980289 | |||||
| chr21:43980290
|
AAC | A | 27 | a0001c0001t0003g0085a0001c0001t0003g0123a0001c0001t0003g0124others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.844-697_844-696del others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43980290 | |||||
| chr21:43980291
|
AC | A | 46 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0041others(43): Show | 46 | HG01257.hp1 HG01257.hp2 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.844-697delC | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980291 | ||||||
| chr21:43980292
|
C | A | 93 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0023others(90): Show | 93 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.844-697C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980292 | ||||||
| chr21:43980295
|
A | C | 4 | a0001c0001t0003g0153a0001c0001t0003g0167a0001c0001t0003g0181others(1): Show | 4 | NA18945.hp2 NA18979.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-694A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980295 | ||||||
| chr21:43980353
|
C | T | 94 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(91): Show | 94 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.844-636C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980353 | ||||||
| chr21:43980369
|
C | T | 3 | a0001c0001t0030g0073a0001c0001t0030g0331a0001c0001t0050g0024 | 3 | HG02257.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.844-620C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980369 | ||||||
| chr21:43980610
|
G | A | 133 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(130): Show | 134 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.844-379G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980610 | ||||||
| chr21:43980654
|
C | T | 4 | a0001c0001t0015g0115a0001c0001t0015g0116a0001c0001t0015g0117others(1): Show | 4 | HG01261.hp2 HG01496.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-335C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980654 | ||||||
| chr21:43980676
|
G | A | 4 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0010g0095others(1): Show | 4 | HG00639.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-313G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980676 | ||||||
| chr21:43980721
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0245 | 2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.844-268C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980721 | ||||||
| chr21:43980802
|
T | C | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.844-187T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980802 | ||||||
| chr21:43980806
|
A | G | 6 | a0001c0001t0019g0069a0001c0001t0019g0323a0001c0001t0019g0330others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-183A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980806 | ||||||
| chr21:43980820
|
C | T | 2 | a0001c0001t0007g0329a0001c0001t0053g0321 | 2 | HG02886.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.844-169C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980820 | ||||||
| chr21:43980900
|
G | A | 23 | a0001c0001t0008g0039a0001c0001t0008g0042a0001c0001t0008g0043others(20): Show | 23 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-89G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980900 | ||||||
| chr21:43980951
|
A | T | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-38A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980951 | ||||||
| chr21:43980959
|
C | T | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-30C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980959 | ||||||
| chr21:43980966
|
T | G | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-23T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980966 | ||||||
| chr21:43980967
|
T | A | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-22T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980967 | ||||||
| chr21:43980968
|
T | A | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-21T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980968 | ||||||
| chr21:43980976
|
T | A | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-13T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980976 | ||||||
| chr21:43980983
|
T | C | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.844-6T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980983 | ||||||
| chr21:43980985
|
C | G | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.844-4C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980985 | ||||||
| chr21:43981196
|
C | G | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1042+9C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981196 | ||||||
| chr21:43981198
|
C | T | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1042+11C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981198 | ||||||
| chr21:43981202
|
C | A | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1042+15C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981202 | ||||||
| chr21:43981204
|
C | A | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1042+17C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981204 | ||||||
| chr21:43981206
|
A | G | 1 | a0002c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1042+19A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981206 | ||||||
| chr21:43981342
|
C | T | 79 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0016others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1042+155C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981342 | ||||||
| chr21:43981491
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1042+304T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981491 | ||||||
| chr21:43981634
|
C | T | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1042+447C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981634 | ||||||
| chr21:43981729
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1042+542T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981729 | ||||||
| chr21:43981731
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1042+544C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981731 | ||||||
| chr21:43981776
|
A | C | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1043-528A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981776 | ||||||
| chr21:43981815
|
G | A | 4 | a0001c0001t0010g0063a0001c0001t0046g0133a0001c0001t0053g0321others(1): Show | 4 | HG02886.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043-489G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981815 | ||||||
| chr21:43981853
|
G | T | 1 | a0001c0001t0024g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1043-451G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981853 | ||||||
| chr21:43981887
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1043-417C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981887 | ||||||
| chr21:43982191
|
C | T | 1 | a0001c0001t0066g0027 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1043-113C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43982191 | ||||||
| chr21:43982234
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1043-70G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43982234 |