Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10162 |
|---|---|
| ensemblid | ENSG00000111684.11 |
| hgncid | 30244 |
| symbol | LPCAT3 |
| name | lysophosphatidylcholine acyltransferase 3 |
| refseq_nuc | NM_005768.6 |
| refseq_prot | NP_005759.4 |
| ensembl_nuc | ENST00000261407.9 |
| ensembl_prot | ENSP00000261407.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 6976185 |
| end | 7018476 |
| strand | - |
| ver | v1.2 |
| region | chr12:6976185-7018476 |
| region5000 | chr12:6971185-7023476 |
| regionname0 | LPCAT3_chr12_6976185_7018476 |
| regionname5000 | LPCAT3_chr12_6971185_7023476 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 487 | 185 | 34 | 36 | 90 | 7 | 17 | 57 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002 | 0/0 | 487 | 78 | 51 | 7 | 17 | 1 | 2 | 14 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0003 | 0/1 | 487 | 9 | 2 | 1 | 2 | 0 | 3 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0004 | 0/0 | 487 | 6 | 0 | 0 | 4 | 0 | 2 | 4 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0005 | 0/0 | 487 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0006 | 0/0 | 487 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0007 | 0/0 | 487 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1464 | 184 | 34 | 36 | 90 | 6 | 17 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0002 | 0/0 | 1464 | 27 | 22 | 4 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0003 | 0/0 | 1464 | 24 | 16 | 3 | 3 | 0 | 2 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0004 | 0/0 | 1464 | 22 | 8 | 0 | 14 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0005 | 0/1 | 1464 | 8 | 2 | 1 | 1 | 0 | 3 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0006 | 0/0 | 1464 | 6 | 0 | 0 | 4 | 0 | 2 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0007 | 0/0 | 1464 | 5 | 5 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0008 | 0/0 | 1464 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0009 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0010 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0011 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| c0012 | 0/0 | 1464 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 772 | 249 | 77 | 43 | 98 | 8 | 21 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| t0002 | 0/0 | 772 | 19 | 5 | 0 | 14 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| t0003 | 0/0 | 772 | 5 | 0 | 0 | 4 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| t0004 | 0/0 | 772 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| t0005 | 0/0 | 772 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| t0006 | 0/0 | 772 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| t0007 | 0/0 | 772 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| t0008 | 0/0 | 772 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| t0009 | 0/0 | 772 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| t0010 | 0/0 | 772 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| t0011 | 0/0 | 772 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0003 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0021 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1464 | 184 | 34 | 36 | 90 | 6 | 17 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0001c0012 | 0/0 | 1464 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0002 | 0/0 | 1464 | 27 | 22 | 4 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0003 | 0/0 | 1464 | 24 | 16 | 3 | 3 | 0 | 2 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0004 | 0/0 | 1464 | 22 | 8 | 0 | 14 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0007 | 0/0 | 1464 | 5 | 5 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0003c0005 | 0/1 | 1464 | 8 | 2 | 1 | 1 | 0 | 3 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0003c0009 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0004c0006 | 0/0 | 1464 | 6 | 0 | 0 | 4 | 0 | 2 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0005c0008 | 0/0 | 1464 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0006c0010 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0007c0011 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2235 | 180 | 32 | 35 | 90 | 6 | 16 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0001c0001t0006 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0001c0001t0008 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0001c0001t0009 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0001c0001t0011 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0001c0012t0001 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0002t0001 | 0/0 | 2235 | 23 | 18 | 4 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0002t0004 | 0/0 | 2235 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0002t0007 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0002t0010 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0003t0001 | 0/0 | 2235 | 24 | 16 | 3 | 3 | 0 | 2 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0004t0001 | 0/0 | 2235 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0004t0002 | 0/0 | 2235 | 19 | 5 | 0 | 14 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0002c0007t0001 | 0/0 | 2235 | 5 | 5 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0003c0005t0001 | 0/1 | 2235 | 8 | 2 | 1 | 1 | 0 | 3 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0003c0009t0001 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0004c0006t0003 | 0/0 | 2235 | 5 | 0 | 0 | 4 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0004c0006t0005 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0005c0008t0001 | 0/0 | 2235 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0006c0010t0001 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| a0007c0011t0001 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | copy fasta | chr12 | 6971185 | 7023476 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0009g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0011g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0012t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0007t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0007t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0007t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0021 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0009t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0004c0006t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0004c0006t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0004c0006t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0004c0006t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0004c0006t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0005c0008t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0005c0008t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0006c0010t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0007c0011t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00280 | hp2 | a0001 | c0012 | t0001 | g0160 | EUR | FIN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0255 | EUR | FIN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0024 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0079 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01175 | hp1 | a0001 | c0001 | t0009 | g0191 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01192 | hp2 | a0003 | c0005 | t0001 | g0019 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0246 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0124 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0266 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01891 | hp2 | a0003 | c0005 | t0001 | g0018 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0091 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0089 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02015 | hp1 | a0005 | c0008 | t0001 | g0103 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02040 | hp2 | a0005 | c0008 | t0001 | g0095 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02056 | hp1 | a0003 | c0009 | t0001 | g0012 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0088 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02129 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02135 | hp2 | a0003 | c0005 | t0001 | g0013 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0140 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02258 | hp1 | a0002 | c0004 | t0002 | g0081 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0123 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0265 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0130 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02602 | hp1 | a0003 | c0005 | t0001 | g0020 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0264 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02622 | hp2 | a0002 | c0004 | t0001 | g0219 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0128 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0245 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02818 | hp1 | a0002 | c0007 | t0001 | g0002 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0240 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0122 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0235 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0260 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0234 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0268 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0129 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02965 | hp1 | a0002 | c0004 | t0002 | g0005 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02976 | hp1 | a0006 | c0010 | t0001 | g0015 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0227 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03017 | hp2 | a0002 | c0003 | t0001 | g0086 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03139 | hp1 | a0003 | c0005 | t0001 | g0022 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0127 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0126 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0218 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03453 | hp2 | a0002 | c0002 | t0004 | g0243 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03486 | hp1 | a0002 | c0004 | t0002 | g0005 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03486 | hp2 | a0002 | c0007 | t0001 | g0002 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0217 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03540 | hp2 | a0002 | c0002 | t0004 | g0242 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03579 | hp1 | a0002 | c0007 | t0001 | g0014 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03688 | hp2 | a0003 | c0005 | t0001 | g0017 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03831 | hp1 | a0004 | c0006 | t0003 | g0256 | SAS | BEB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04115 | hp2 | a0004 | c0006 | t0005 | g0259 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04228 | hp1 | a0003 | c0005 | t0001 | g0016 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04228 | hp2 | a0002 | c0003 | t0001 | g0090 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18522 | hp1 | a0002 | c0004 | t0002 | g0026 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0247 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18941 | hp2 | a0002 | c0004 | t0002 | g0228 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18942 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18950 | hp1 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18952 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18981 | hp1 | a0002 | c0004 | t0002 | g0221 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18999 | hp1 | a0002 | c0004 | t0002 | g0225 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19009 | hp2 | a0002 | c0004 | t0002 | g0224 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19011 | hp1 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19011 | hp2 | a0004 | c0006 | t0003 | g0257 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19030 | hp2 | a0002 | c0002 | t0010 | g0267 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19059 | hp1 | a0002 | c0004 | t0002 | g0239 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19072 | hp2 | a0002 | c0004 | t0002 | g0222 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19074 | hp2 | a0004 | c0006 | t0003 | g0010 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19076 | hp1 | a0004 | c0006 | t0003 | g0258 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19076 | hp2 | a0007 | c0011 | t0001 | g0110 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19078 | hp2 | a0002 | c0004 | t0002 | g0220 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19085 | hp1 | a0004 | c0006 | t0003 | g0010 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19089 | hp2 | a0002 | c0004 | t0002 | g0238 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19090 | hp1 | a0002 | c0004 | t0002 | g0223 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19091 | hp1 | a0002 | c0004 | t0002 | g0226 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0249 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19240 | hp2 | a0002 | c0004 | t0002 | g0082 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA20905 | hp2 | a0001 | c0001 | t0011 | g0097 | SAS | GIH | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0253 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02559 | hp2 | a0002 | c0007 | t0001 | g0002 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0131 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG06807 | hp1 | a0002 | c0002 | t0007 | g0025 | AFR | USA | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | USA | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0125 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA21309 | hp2 | a0002 | c0007 | t0001 | g0011 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0005 | t0001 | g0021 | REF | REF | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0094 | REF | REF | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6977136
|
G | A | 1 | a0002 | 19 | HG02258.hp1 HG02965.hp1 HG03486.hp1 others(16): Show |
splice_region_variant | LOW | c.*10C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 12/13 | chr12 | 6977136 | ||||||
| chr12:6977740
|
A | G | 1 | a0006 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1046T>C | p.Ile349Thr | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 10/13 | 1098/2235 | 1046/1464 | 349/487 | chr12 | 6977740 | ||
| chr12:6981031
|
A | G | 4 | a0002a0003a0004others(1): Show | 94 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(91): Show |
missense_variant | MODERATE | c.650T>C | p.Ile217Thr | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/13 | 702/2235 | 650/1464 | 217/487 | chr12 | 6981031 | ||
| chr12:6982711
|
T | C | 1 | a0005 | 2 | HG02015.hp1 HG02040.hp2 |
missense_variant | MODERATE | c.331A>G | p.Ile111Val | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 3/13 | 383/2235 | 331/1464 | 111/487 | chr12 | 6982711 | ||
| chr12:6982720
|
C | G | 1 | a0007 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.322G>C | p.Gly108Arg | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 3/13 | 374/2235 | 322/1464 | 108/487 | chr12 | 6982720 | ||
| chr12:6982738
|
G | A | 1 | a0004 | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
missense_variant | MODERATE | c.304C>T | p.Leu102Phe | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 3/13 | 356/2235 | 304/1464 | 102/487 | chr12 | 6982738 | ||
| chr12:6983504
|
A | G | 1 | a0003 | 9 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(6): Show |
missense_variant | MODERATE | c.187T>C | p.Phe63Leu | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 2/13 | 239/2235 | 187/1464 | 63/487 | chr12 | 6983504 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6977424
|
G | A | 1 | a0001c0012 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.1290C>T | p.Leu430Leu | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 11/13 | 1342/2235 | 1290/1464 | 430/487 | chr12 | 6977424 | ||
| chr12:6977514
|
G | A | 1 | a0003c0009 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.1200C>T | p.Leu400Leu | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 11/13 | 1252/2235 | 1200/1464 | 400/487 | chr12 | 6977514 | ||
| chr12:6981860
|
G | A | 1 | a0002c0004 | 22 | HG02258.hp1 HG02622.hp2 HG02965.hp1 others(19): Show |
synonymous_variant | LOW | c.411C>T | p.Tyr137Tyr | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 4/13 | 463/2235 | 411/1464 | 137/487 | chr12 | 6981860 | ||
| chr12:6982757
|
C | T | 7 | a0002c0002a0002c0004a0002c0007others(4): Show | 70 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(67): Show |
synonymous_variant | LOW | c.285G>A | p.Leu95Leu | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 3/13 | 337/2235 | 285/1464 | 95/487 | chr12 | 6982757 | ||
| chr12:7018368
|
C | G | 4 | a0002c0007a0003c0005a0003c0009others(1): Show | 15 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(12): Show |
synonymous_variant | LOW | c.57G>C | p.Leu19Leu | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/13 | 109/2235 | 57/1464 | 19/487 | chr12 | 7018368 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6976224
|
G | C | 1 | a0004c0006t0005 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*680C>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 13/13 | 922 | chr12 | 6976224 | |||||
| chr12:6976313
|
T | C | 1 | a0001c0001t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 13/13 | 833 | chr12 | 6976313 | |||||
| chr12:6976409
|
C | T | 1 | a0002c0002t0007 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*495G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 13/13 | 737 | chr12 | 6976409 | |||||
| chr12:6976418
|
T | C | 1 | a0001c0001t0009 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*486A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 13/13 | 728 | chr12 | 6976418 | |||||
| chr12:6976435
|
C | T | 1 | a0001c0001t0006 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*469G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 13/13 | 711 | chr12 | 6976435 | |||||
| chr12:6976447
|
G | A | 1 | a0002c0002t0010 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*457C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 13/13 | 699 | chr12 | 6976447 | |||||
| chr12:6976542
|
T | C | 1 | a0002c0002t0004 | 2 | HG03453.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*362A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 13/13 | 604 | chr12 | 6976542 | |||||
| chr12:6976663
|
C | T | 2 | a0004c0006t0003a0004c0006t0005 | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*241G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 13/13 | 483 | chr12 | 6976663 | |||||
| chr12:6976680
|
G | A | 1 | a0004c0006t0003 | 5 | HG03831.hp1 NA19011.hp2 NA19074.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*224C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 13/13 | 466 | chr12 | 6976680 | |||||
| chr12:6976738
|
C | A | 1 | a0001c0001t0011 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*166G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 13/13 | 408 | chr12 | 6976738 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:6977054
|
T | G | 4 | a0002c0004t0002g0005a0002c0004t0002g0026a0002c0004t0002g0081others(1): Show | 5 | HG02258.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.*12+80A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 12/12 | chr12 | 6977054 | ||||||
| chr12:6977132
|
AC | A | 15 | a0002c0004t0002g0001a0002c0004t0002g0005a0002c0004t0002g0026others(12): Show | 19 | HG02258.hp1 HG02965.hp1 HG03486.hp1 others(16): Show |
splice_donor_variant&intron_variant | HIGH | c.*12+1delG | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 12/12 | chr12 | 6977132 | ||||||
| chr12:6977769
|
G | A | 1 | a0002c0003t0001g0088 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1041-24C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 9/12 | chr12 | 6977769 | ||||||
| chr12:6977969
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1041-224T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 9/12 | chr12 | 6977969 | ||||||
| chr12:6978519
|
T | C | 20 | a0002c0002t0001g0085a0002c0002t0007g0025a0002c0004t0001g0218others(17): Show | 24 | HG02258.hp1 HG02622.hp2 HG02965.hp1 others(21): Show |
intron_variant | MODIFIER | c.874-12A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 8/12 | chr12 | 6978519 | ||||||
| chr12:6978549
|
T | C | 86 | a0001c0001t0001g0187a0002c0002t0001g0085a0002c0002t0001g0217others(83): Show | 95 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.874-42A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 8/12 | chr12 | 6978549 | ||||||
| chr12:6978748
|
G | GCA | 10 | a0002c0003t0001g0088a0003c0005t0001g0013a0003c0005t0001g0016others(7): Show | 10 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.787-61_787-60dupTG | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 7/12 | chr12 | 6978748 | ||||||
| chr12:6978886
|
C | T | 3 | a0001c0001t0001g0099a0005c0008t0001g0095a0005c0008t0001g0103 | 3 | HG02015.hp1 HG02040.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.787-197G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 7/12 | chr12 | 6978886 | ||||||
| chr12:6979000
|
A | G | 4 | a0001c0001t0001g0115a0001c0001t0001g0207a0001c0001t0001g0209others(1): Show | 4 | HG00609.hp2 NA18947.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-311T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 7/12 | chr12 | 6979000 | ||||||
| chr12:6979105
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0269 | 3 | NA18944.hp2 NA19002.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.786+366C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 7/12 | chr12 | 6979105 | ||||||
| chr12:6979156
|
TAGGATGG others(3): Show |
T | 1 | a0007c0011t0001g0110 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.786+305_786+314del others(10): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 7/12 | chr12 | 6979156 | ||||||
| chr12:6979243
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.786+228C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 7/12 | chr12 | 6979243 | ||||||
| chr12:6979402
|
A | G | 3 | a0002c0004t0001g0218a0002c0004t0001g0219a0002c0004t0001g0227 | 3 | HG02622.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.786+69T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 7/12 | chr12 | 6979402 | ||||||
| chr12:6979967
|
G | T | 1 | a0002c0002t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.678-388C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6979967 | ||||||
| chr12:6980009
|
C | T | 10 | a0002c0002t0001g0245a0002c0002t0001g0246a0002c0002t0001g0247others(7): Show | 10 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.678-430G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980009 | ||||||
| chr12:6980021
|
C | CT | 68 | a0001c0001t0001g0053a0001c0001t0001g0074a0001c0001t0001g0105others(65): Show | 74 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.678-443dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980021 | ||||||
| chr12:6980021
|
C | CTT | 21 | a0001c0001t0001g0039a0002c0002t0001g0085a0002c0002t0001g0240others(18): Show | 24 | HG00642.hp2 HG01891.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.678-444_678-443dup others(2): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980021 | ||||||
| chr12:6980021
|
CT | C | 8 | a0001c0001t0001g0034a0001c0001t0001g0075a0001c0001t0001g0133others(5): Show | 8 | HG01169.hp1 HG01169.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.678-443delA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980021 | ||||||
| chr12:6980079
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.678-500C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980079 | ||||||
| chr12:6980401
|
G | A | 1 | a0002c0002t0001g0246 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.677+603C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980401 | ||||||
| chr12:6980451
|
A | G | 63 | a0002c0002t0001g0085a0002c0002t0001g0217a0002c0002t0001g0240others(60): Show | 70 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.677+553T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980451 | ||||||
| chr12:6980548
|
GTC | G | 11 | a0002c0004t0002g0001a0002c0004t0002g0220a0002c0004t0002g0221others(8): Show | 14 | NA18941.hp2 NA18942.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.677+454_677+455del others(2): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980548 | ||||||
| chr12:6980593
|
G | A | 1 | a0002c0002t0007g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.677+411C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980593 | ||||||
| chr12:6980828
|
G | A | 2 | a0002c0007t0001g0002a0002c0007t0001g0011 | 4 | HG02559.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.677+176C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980828 | ||||||
| chr12:6980934
|
GCT | G | 12 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(9): Show | 12 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.677+68_677+69delAG | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980934 | ||||||
| chr12:6981423
|
G | C | 6 | a0002c0002t0001g0240a0002c0002t0001g0263a0002c0002t0001g0264others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.498+172C>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 5/12 | chr12 | 6981423 | ||||||
| chr12:6981474
|
G | T | 10 | a0002c0002t0001g0245a0002c0002t0001g0246a0002c0002t0001g0247others(7): Show | 10 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.498+121C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 5/12 | chr12 | 6981474 | ||||||
| chr12:6981581
|
G | A | 36 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(33): Show | 38 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.498+14C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 5/12 | chr12 | 6981581 | ||||||
| chr12:6981938
|
C | T | 9 | a0002c0002t0001g0240a0002c0002t0001g0260a0002c0002t0001g0261others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.367-34G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 3/12 | chr12 | 6981938 | ||||||
| chr12:6982150
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.367-246G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 3/12 | chr12 | 6982150 | ||||||
| chr12:6982244
|
G | T | 1 | a0002c0007t0001g0011 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.367-340C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 3/12 | chr12 | 6982244 | ||||||
| chr12:6982247
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.367-343G>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 3/12 | chr12 | 6982247 | ||||||
| chr12:6982330
|
T | G | 1 | a0007c0011t0001g0110 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.366+346A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 3/12 | chr12 | 6982330 | ||||||
| chr12:6982601
|
C | T | 6 | a0002c0002t0001g0240a0002c0002t0001g0263a0002c0002t0001g0264others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+75G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 3/12 | chr12 | 6982601 | ||||||
| chr12:6982966
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.260-184T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 2/12 | chr12 | 6982966 | ||||||
| chr12:6983131
|
C | CT | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.259+300dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 2/12 | chr12 | 6983131 | ||||||
| chr12:6983223
|
C | A | 1 | a0002c0003t0001g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.259+209G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 2/12 | chr12 | 6983223 | ||||||
| chr12:6983278
|
A | G | 1 | a0007c0011t0001g0110 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.259+154T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 2/12 | chr12 | 6983278 | ||||||
| chr12:6983334
|
T | TTCCCTAC others(11): Show |
1 | a0007c0011t0001g0110 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.259+80_259+97dupGA others(16): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 2/12 | chr12 | 6983334 | ||||||
| chr12:6983626
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.152-87C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6983626 | ||||||
| chr12:6983638
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.152-99T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6983638 | ||||||
| chr12:6983641
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.152-102C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6983641 | ||||||
| chr12:6984304
|
A | G | 1 | a0002c0002t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.152-765T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6984304 | ||||||
| chr12:6984426
|
T | C | 6 | a0002c0002t0001g0240a0002c0002t0001g0263a0002c0002t0001g0264others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-887A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6984426 | ||||||
| chr12:6984649
|
C | T | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152-1110G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6984649 | ||||||
| chr12:6984699
|
A | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0207a0001c0001t0001g0209 | 3 | HG00609.hp2 NA18947.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.152-1160T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6984699 | ||||||
| chr12:6984732
|
G | A | 11 | a0002c0002t0001g0240a0002c0002t0001g0260a0002c0002t0001g0261others(8): Show | 11 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-1193C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6984732 | ||||||
| chr12:6984772
|
A | C | 1 | a0002c0002t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.152-1233T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6984772 | ||||||
| chr12:6984807
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.152-1268G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6984807 | ||||||
| chr12:6984864
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-1325G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6984864 | ||||||
| chr12:6985089
|
TA | T | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(219): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.152-1551delT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985089 | ||||||
| chr12:6985089
|
TAA | T | 18 | a0001c0001t0001g0141a0001c0001t0001g0187a0002c0002t0001g0244others(15): Show | 18 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.152-1552_152-1551d others(4): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985089 | ||||||
| chr12:6985163
|
G | A | 1 | a0002c0002t0001g0249 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.152-1624C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985163 | ||||||
| chr12:6985167
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.152-1628C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985167 | ||||||
| chr12:6985173
|
T | C | 42 | a0001c0001t0001g0187a0002c0002t0001g0085a0002c0002t0001g0217others(39): Show | 47 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.152-1634A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985173 | ||||||
| chr12:6985247
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0069 | 2 | HG02071.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.152-1708A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985247 | ||||||
| chr12:6985321
|
G | A | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-1782C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985321 | ||||||
| chr12:6985647
|
A | G | 3 | a0002c0004t0001g0218a0002c0004t0001g0219a0002c0004t0001g0227 | 3 | HG02622.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.152-2108T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985647 | ||||||
| chr12:6985651
|
T | C | 3 | a0002c0004t0001g0218a0002c0004t0001g0219a0002c0004t0001g0227 | 3 | HG02622.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.152-2112A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985651 | ||||||
| chr12:6985771
|
G | GT | 28 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0084others(25): Show | 35 | HG00597.hp2 HG02258.hp1 HG02559.hp2 others(32): Show |
intron_variant | MODIFIER | c.152-2233dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985771 | ||||||
| chr12:6985771
|
G | T | 1 | a0002c0004t0002g0238 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.152-2232C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985771 | ||||||
| chr12:6985963
|
C | T | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-2424G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985963 | ||||||
| chr12:6986067
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.152-2528C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986067 | ||||||
| chr12:6986214
|
A | G | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152-2675T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986214 | ||||||
| chr12:6986331
|
T | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0181 | 2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.152-2792A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986331 | ||||||
| chr12:6986351
|
TTAA | T | 18 | a0002c0004t0001g0218a0002c0004t0001g0219a0002c0004t0001g0227others(15): Show | 22 | HG02258.hp1 HG02622.hp2 HG02965.hp1 others(19): Show |
intron_variant | MODIFIER | c.152-2815_152-2813d others(5): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986351 | ||||||
| chr12:6986383
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-2844T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986383 | ||||||
| chr12:6986580
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0183 | 2 | HG01169.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.152-3041G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986580 | ||||||
| chr12:6986746
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.152-3207G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986746 | ||||||
| chr12:6986795
|
C | CA | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(62): Show | 67 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.152-3257dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986795 | ||||||
| chr12:6986795
|
C | CAA | 14 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0053others(11): Show | 14 | HG00438.hp1 HG00597.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-3258_152-3257d others(4): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986795 | ||||||
| chr12:6986795
|
CA | C | 15 | a0001c0001t0001g0189a0002c0002t0007g0025a0002c0004t0002g0001others(12): Show | 19 | HG00099.hp1 HG04115.hp2 HG06807.hp1 others(16): Show |
intron_variant | MODIFIER | c.152-3257delT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986795 | ||||||
| chr12:6986856
|
T | C | 13 | a0002c0007t0001g0002a0002c0007t0001g0011a0002c0007t0001g0014others(10): Show | 15 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.152-3317A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986856 | ||||||
| chr12:6986884
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.152-3345G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986884 | ||||||
| chr12:6986916
|
C | T | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-3377G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6986916 | ||||||
| chr12:6987044
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.152-3505G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6987044 | ||||||
| chr12:6987045
|
G | A | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152-3506C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6987045 | ||||||
| chr12:6987111
|
C | CA | 72 | a0002c0002t0001g0085a0002c0002t0001g0217a0002c0002t0001g0244others(69): Show | 81 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.152-3573dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6987111 | ||||||
| chr12:6987111
|
C | CAA | 12 | a0002c0002t0001g0240a0002c0002t0001g0260a0002c0002t0001g0261others(9): Show | 12 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-3574_152-3573d others(4): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6987111 | ||||||
| chr12:6987268
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.152-3729C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6987268 | ||||||
| chr12:6987420
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.152-3881T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6987420 | ||||||
| chr12:6987421
|
T | A | 1 | a0002c0002t0010g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.152-3882A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6987421 | ||||||
| chr12:6987988
|
G | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.152-4449C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6987988 | ||||||
| chr12:6988108
|
A | C | 11 | a0002c0004t0002g0001a0002c0004t0002g0220a0002c0004t0002g0221others(8): Show | 14 | NA18941.hp2 NA18942.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-4569T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988108 | ||||||
| chr12:6988345
|
G | A | 9 | a0003c0005t0001g0013a0003c0005t0001g0016a0003c0005t0001g0017others(6): Show | 9 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-4806C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988345 | ||||||
| chr12:6988504
|
G | A | 11 | a0002c0004t0002g0001a0002c0004t0002g0220a0002c0004t0002g0221others(8): Show | 14 | NA18941.hp2 NA18942.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-4965C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988504 | ||||||
| chr12:6988510
|
G | A | 1 | a0003c0005t0001g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.152-4971C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988510 | ||||||
| chr12:6988696
|
C | T | 3 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0262 | 3 | HG02809.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.152-5157G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988696 | ||||||
| chr12:6988709
|
C | A | 1 | a0002c0002t0010g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.152-5170G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988709 | ||||||
| chr12:6988773
|
T | C | 1 | a0002c0002t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.152-5234A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988773 | ||||||
| chr12:6988806
|
A | C | 11 | a0002c0004t0002g0001a0002c0004t0002g0220a0002c0004t0002g0221others(8): Show | 14 | NA18941.hp2 NA18942.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-5267T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988806 | ||||||
| chr12:6988828
|
G | A | 1 | a0002c0002t0007g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.152-5289C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988828 | ||||||
| chr12:6988848
|
C | T | 9 | a0002c0002t0001g0240a0002c0002t0001g0260a0002c0002t0001g0261others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-5309G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988848 | ||||||
| chr12:6988856
|
G | A | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-5317C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988856 | ||||||
| chr12:6988865
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0185 | 2 | HG00558.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.152-5326C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988865 | ||||||
| chr12:6988878
|
G | A | 2 | a0005c0008t0001g0095a0005c0008t0001g0103 | 2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.152-5339C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988878 | ||||||
| chr12:6989081
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.152-5542G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989081 | ||||||
| chr12:6989312
|
T | G | 1 | a0007c0011t0001g0110 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.152-5773A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989312 | ||||||
| chr12:6989313
|
G | GT | 12 | a0001c0001t0001g0038a0001c0001t0001g0104a0001c0001t0001g0119others(9): Show | 12 | HG00423.hp1 HG00438.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-5775dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989313 | ||||||
| chr12:6989313
|
G | T | 1 | a0007c0011t0001g0110 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.152-5774C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989313 | ||||||
| chr12:6989313
|
GT | G | 62 | a0001c0001t0001g0173a0001c0001t0001g0187a0002c0002t0001g0085others(59): Show | 66 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.152-5775delA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989313 | ||||||
| chr12:6989677
|
G | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0169 | 2 | HG00438.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.152-6138C>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989677 | ||||||
| chr12:6989725
|
AAGTGCTG others(10): Show |
A | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.152-6203_152-6187d others(19): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989725 | ||||||
| chr12:6989775
|
G | A | 4 | a0002c0004t0002g0005a0002c0004t0002g0026a0002c0004t0002g0081others(1): Show | 5 | HG02258.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-6236C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989775 | ||||||
| chr12:6989786
|
C | A | 4 | a0002c0004t0002g0005a0002c0004t0002g0026a0002c0004t0002g0081others(1): Show | 5 | HG02258.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-6247G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989786 | ||||||
| chr12:6989943
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0174 | 2 | HG00597.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.152-6404G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989943 | ||||||
| chr12:6990128
|
C | T | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-6589G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990128 | ||||||
| chr12:6990199
|
A | C | 1 | a0001c0001t0001g0096 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.152-6660T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990199 | ||||||
| chr12:6990205
|
TAAATAA | T | 3 | a0002c0004t0001g0218a0002c0004t0001g0219a0002c0004t0001g0227 | 3 | HG02622.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.152-6672_152-6667d others(8): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990205 | ||||||
| chr12:6990224
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.152-6685A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990224 | ||||||
| chr12:6990230
|
C | T | 10 | a0002c0002t0001g0245a0002c0002t0001g0246a0002c0002t0001g0247others(7): Show | 10 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-6691G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990230 | ||||||
| chr12:6990281
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0214 | 2 | HG00423.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.152-6742C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990281 | ||||||
| chr12:6990292
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0166 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152-6753C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990292 | ||||||
| chr12:6990365
|
C | G | 1 | a0001c0001t0001g0119 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.152-6826G>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990365 | ||||||
| chr12:6990368
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.152-6829C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990368 | ||||||
| chr12:6990370
|
G | A | 2 | a0002c0007t0001g0002a0002c0007t0001g0011 | 4 | HG02559.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-6831C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990370 | ||||||
| chr12:6990378
|
G | A | 1 | a0002c0004t0001g0219 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-6839C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990378 | ||||||
| chr12:6990381
|
C | T | 10 | a0002c0002t0001g0245a0002c0002t0001g0246a0002c0002t0001g0247others(7): Show | 10 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-6842G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990381 | ||||||
| chr12:6990526
|
A | AAAAT | 75 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0032others(72): Show | 76 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.152-6991_152-6988d others(6): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990526 | ||||||
| chr12:6990526
|
A | AAAATAAA others(1): Show |
8 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0033others(5): Show | 9 | HG01109.hp2 HG02040.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-6995_152-6988d others(10): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990526 | ||||||
| chr12:6990526
|
AAAAT | A | 22 | a0001c0001t0001g0133a0002c0002t0001g0217a0002c0002t0001g0244others(19): Show | 23 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-6991_152-6988d others(6): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990526 | ||||||
| chr12:6990526
|
AAAATAAA others(9): Show |
A | 1 | a0001c0001t0009g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.152-7003_152-6988d others(18): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990526 | ||||||
| chr12:6990547
|
AAATAAAT others(13): Show |
A | 2 | a0002c0007t0001g0002a0002c0007t0001g0011 | 4 | HG02559.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-7028_152-7009d others(22): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990547 | ||||||
| chr12:6990555
|
AAATAAAT others(5): Show |
A | 1 | a0002c0002t0001g0268 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152-7028_152-7017d others(14): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990555 | ||||||
| chr12:6990559
|
AAATAAAT others(1): Show |
A | 11 | a0002c0007t0001g0014a0003c0005t0001g0013a0003c0005t0001g0016others(8): Show | 11 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-7028_152-7021d others(10): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990559 | ||||||
| chr12:6990563
|
AAATT | A | 11 | a0001c0001t0001g0054a0001c0001t0001g0067a0001c0001t0001g0186others(8): Show | 11 | HG00099.hp2 HG01106.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-7028_152-7025d others(6): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990563 | ||||||
| chr12:6990567
|
T | A | 29 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0043others(26): Show | 29 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.152-7028A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990567 | ||||||
| chr12:6990712
|
C | A | 11 | a0002c0004t0002g0001a0002c0004t0002g0220a0002c0004t0002g0221others(8): Show | 14 | NA18941.hp2 NA18942.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-7173G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990712 | ||||||
| chr12:6990831
|
C | T | 2 | a0002c0007t0001g0002a0002c0007t0001g0011 | 4 | HG02559.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-7292G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990831 | ||||||
| chr12:6990916
|
C | CA | 57 | a0001c0001t0001g0138a0001c0001t0001g0212a0002c0002t0001g0085others(54): Show | 62 | HG00423.hp2 HG01069.hp2 HG01192.hp2 others(59): Show |
intron_variant | MODIFIER | c.152-7378dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990916 | ||||||
| chr12:6990916
|
C | CAA | 20 | a0002c0002t0001g0244a0002c0002t0001g0246a0002c0002t0001g0255others(17): Show | 24 | HG00323.hp1 HG00642.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.152-7379_152-7378d others(4): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990916 | ||||||
| chr12:6990916
|
C | CAAA | 10 | a0002c0002t0001g0245a0002c0002t0001g0247a0002c0002t0001g0248others(7): Show | 10 | HG00738.hp2 HG01358.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-7380_152-7378d others(5): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990916 | ||||||
| chr12:6991942
|
A | G | 1 | a0002c0002t0007g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.152-8403T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6991942 | ||||||
| chr12:6991990
|
C | T | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-8451G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6991990 | ||||||
| chr12:6992150
|
T | C | 9 | a0002c0002t0001g0240a0002c0002t0001g0260a0002c0002t0001g0261others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-8611A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6992150 | ||||||
| chr12:6992240
|
G | A | 10 | a0002c0002t0001g0245a0002c0002t0001g0246a0002c0002t0001g0247others(7): Show | 10 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-8701C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6992240 | ||||||
| chr12:6992448
|
C | T | 62 | a0002c0002t0001g0085a0002c0002t0001g0217a0002c0002t0001g0240others(59): Show | 69 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.152-8909G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6992448 | ||||||
| chr12:6992589
|
C | T | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-9050G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6992589 | ||||||
| chr12:6992601
|
T | C | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152-9062A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6992601 | ||||||
| chr12:6992880
|
C | T | 1 | a0002c0002t0001g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152-9341G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6992880 | ||||||
| chr12:6992881
|
A | C | 41 | a0002c0002t0001g0085a0002c0002t0001g0217a0002c0002t0001g0244others(38): Show | 46 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.152-9342T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6992881 | ||||||
| chr12:6993049
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.152-9510G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6993049 | ||||||
| chr12:6993099
|
A | G | 1 | a0002c0003t0001g0024 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.152-9560T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6993099 | ||||||
| chr12:6993158
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.152-9619G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6993158 | ||||||
| chr12:6993334
|
T | TGAGGGAG others(25): Show |
3 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0262 | 3 | HG02809.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.152-9827_152-9796d others(34): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6993334 | ||||||
| chr12:6993345
|
A | G | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-9806T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6993345 | ||||||
| chr12:6993374
|
C | T | 4 | a0002c0004t0002g0005a0002c0004t0002g0026a0002c0004t0002g0081others(1): Show | 5 | HG02258.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-9835G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6993374 | ||||||
| chr12:6993443
|
A | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(32): Show | 37 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.152-9904T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6993443 | ||||||
| chr12:6993746
|
C | T | 21 | a0002c0003t0001g0006a0002c0003t0001g0007a0002c0003t0001g0024others(18): Show | 23 | HG00423.hp2 HG01069.hp2 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.152-10207G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6993746 | ||||||
| chr12:6993989
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.152-10450C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6993989 | ||||||
| chr12:6994124
|
C | A | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-10585G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6994124 | ||||||
| chr12:6994283
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.152-10744G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6994283 | ||||||
| chr12:6994293
|
C | T | 1 | a0002c0002t0001g0268 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152-10754G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6994293 | ||||||
| chr12:6994374
|
A | AT | 3 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0262 | 3 | HG02809.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.152-10836dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6994374 | ||||||
| chr12:6994487
|
C | T | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152-10948G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6994487 | ||||||
| chr12:6994488
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.152-10949C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6994488 | ||||||
| chr12:6994568
|
G | C | 1 | a0001c0001t0008g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.152-11029C>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6994568 | ||||||
| chr12:6994730
|
C | T | 9 | a0002c0002t0001g0240a0002c0002t0001g0260a0002c0002t0001g0261others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-11191G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6994730 | ||||||
| chr12:6994992
|
GTTCTAAC others(3): Show |
G | 1 | a0001c0001t0001g0119 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.152-11463_152-1145 others(14): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6994992 | ||||||
| chr12:6995023
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.152-11484A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6995023 | ||||||
| chr12:6995121
|
CT | C | 225 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(222): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.152-11583delA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6995121 | ||||||
| chr12:6995122
|
T | C | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.152-11583A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6995122 | ||||||
| chr12:6995136
|
T | A | 4 | a0002c0003t0001g0122a0002c0003t0001g0123a0002c0003t0001g0234others(1): Show | 4 | HG02258.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-11597A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6995136 | ||||||
| chr12:6995413
|
G | A | 1 | a0002c0003t0001g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.152-11874C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6995413 | ||||||
| chr12:6995499
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.152-11960A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6995499 | ||||||
| chr12:6996093
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.152-12554C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6996093 | ||||||
| chr12:6996142
|
C | CA | 4 | a0002c0002t0001g0244a0002c0002t0001g0255a0002c0002t0004g0242others(1): Show | 4 | HG00323.hp1 HG00642.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-12604dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6996142 | ||||||
| chr12:6996287
|
A | G | 1 | a0002c0002t0007g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.152-12748T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6996287 | ||||||
| chr12:6996309
|
A | G | 1 | a0002c0003t0001g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.152-12770T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6996309 | ||||||
| chr12:6996372
|
C | T | 1 | a0003c0005t0001g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.152-12833G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6996372 | ||||||
| chr12:6996444
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.152-12905A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6996444 | ||||||
| chr12:6996673
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-13134A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6996673 | ||||||
| chr12:6996714
|
T | C | 13 | a0002c0007t0001g0002a0002c0007t0001g0011a0002c0007t0001g0014others(10): Show | 15 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.152-13175A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6996714 | ||||||
| chr12:6996889
|
G | A | 8 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0262others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-13350C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6996889 | ||||||
| chr12:6997010
|
GA | G | 60 | a0002c0002t0001g0217a0002c0002t0001g0244a0002c0002t0001g0245others(57): Show | 67 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.152-13472delT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997010 | ||||||
| chr12:6997091
|
C | T | 1 | a0002c0002t0004g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-13552G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997091 | ||||||
| chr12:6997376
|
A | T | 1 | a0001c0001t0001g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.152-13837T>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997376 | ||||||
| chr12:6997377
|
TTATG | T | 4 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(1): Show | 5 | HG03831.hp1 NA19011.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-13842_152-1383 others(8): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997377 | ||||||
| chr12:6997379
|
A | ATG | 52 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0050others(49): Show | 57 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.152-13842_152-1384 others(6): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
A | ATGTG | 50 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0030others(47): Show | 50 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.152-13844_152-1384 others(8): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
A | ATGTGTG | 18 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(15): Show | 20 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.152-13846_152-1384 others(10): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
A | ATGTGTGT others(1): Show |
6 | a0001c0001t0001g0036a0001c0001t0001g0066a0001c0001t0001g0204others(3): Show | 6 | HG02071.hp2 HG03453.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-13848_152-1384 others(12): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0207a0002c0002t0004g0242a0002c0004t0002g0223 | 3 | HG00609.hp2 HG03540.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.152-13850_152-1384 others(14): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0001g0032 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.152-13852_152-1384 others(16): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
A | G | 2 | a0001c0001t0001g0034a0004c0006t0005g0259 | 2 | HG04115.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.152-13840T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
ATG | A | 19 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0084others(16): Show | 19 | HG00280.hp1 HG00738.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-13842_152-1384 others(6): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
ATGTG | A | 23 | a0001c0001t0001g0093a0001c0001t0001g0102a0001c0001t0001g0104others(20): Show | 25 | HG01192.hp1 HG01261.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.152-13844_152-1384 others(8): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
ATGTGTG | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0166a0002c0002t0001g0085others(3): Show | 6 | HG01891.hp2 HG02056.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-13846_152-1384 others(10): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
ATGTGTGT others(1): Show |
A | 6 | a0003c0005t0001g0013a0003c0005t0001g0016a0003c0005t0001g0017others(3): Show | 6 | HG01192.hp2 HG02135.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-13848_152-1384 others(12): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
ATGTGTGT others(3): Show |
A | 10 | a0002c0003t0001g0024a0002c0003t0001g0079a0002c0003t0001g0086others(7): Show | 10 | HG00423.hp2 HG01069.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-13850_152-1384 others(14): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
ATGTGTGT others(5): Show |
A | 2 | a0002c0007t0001g0002a0002c0007t0001g0011 | 4 | HG02559.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-13852_152-1384 others(16): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
ATGTGTGT others(13): Show |
A | 3 | a0002c0004t0001g0218a0002c0004t0001g0219a0002c0004t0001g0227 | 3 | HG02622.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.152-13860_152-1384 others(24): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997379
|
ATGTGTGT others(15): Show |
A | 1 | a0001c0001t0011g0097 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.152-13862_152-1384 others(26): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997379 | ||||||
| chr12:6997383
|
G | A | 3 | a0002c0002t0001g0250a0002c0002t0001g0251a0002c0002t0001g0253 | 3 | HG00738.hp2 HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.152-13844C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997383 | ||||||
| chr12:6997385
|
G | A | 6 | a0002c0002t0001g0246a0002c0002t0001g0247a0002c0002t0001g0248others(3): Show | 6 | HG01261.hp1 HG01358.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-13846C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997385 | ||||||
| chr12:6997387
|
G | A | 1 | a0002c0002t0001g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.152-13848C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997387 | ||||||
| chr12:6997428
|
T | TGTG | 3 | a0001c0001t0001g0167a0001c0001t0001g0173a0001c0001t0001g0237 | 3 | HG02080.hp1 HG03669.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.152-13890_152-1388 others(7): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997428 | ||||||
| chr12:6997428
|
T | TGTGTG | 3 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0001g0193 | 3 | HG01168.hp1 HG01168.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.152-13890_152-1388 others(9): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997428 | ||||||
| chr12:6997428
|
T | TGTGTGTG | 3 | a0001c0001t0001g0106a0001c0001t0001g0115a0002c0002t0001g0244 | 3 | HG00642.hp2 HG02280.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.152-13890_152-1388 others(11): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997428 | ||||||
| chr12:6997429
|
T | G | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.152-13890A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997429 | ||||||
| chr12:6997567
|
C | T | 1 | a0002c0002t0007g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.152-14028G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997567 | ||||||
| chr12:6997590
|
C | CT | 10 | a0002c0002t0007g0025a0002c0004t0002g0001a0002c0004t0002g0220others(7): Show | 13 | HG06807.hp1 NA18941.hp2 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-14052dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997590 | ||||||
| chr12:6997620
|
C | T | 1 | a0002c0002t0007g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.152-14081G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997620 | ||||||
| chr12:6997655
|
C | T | 8 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0262others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-14116G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997655 | ||||||
| chr12:6997914
|
A | G | 13 | a0002c0007t0001g0002a0002c0007t0001g0011a0002c0007t0001g0014others(10): Show | 15 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.152-14375T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997914 | ||||||
| chr12:6997966
|
G | C | 1 | a0002c0004t0002g0226 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.152-14427C>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997966 | ||||||
| chr12:6998042
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.152-14503C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6998042 | ||||||
| chr12:6998137
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.152-14598G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6998137 | ||||||
| chr12:6998155
|
ACAGGAAT others(4): Show |
A | 1 | a0002c0002t0001g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-14627_152-1461 others(15): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6998155 | ||||||
| chr12:6998411
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0169 | 2 | HG00438.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.152-14872G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6998411 | ||||||
| chr12:6998543
|
C | T | 4 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(1): Show | 5 | HG03831.hp1 NA19011.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-15004G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6998543 | ||||||
| chr12:6998569
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.152-15030C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6998569 | ||||||
| chr12:6998790
|
A | C | 4 | a0002c0002t0001g0247a0002c0002t0001g0248a0002c0002t0001g0249others(1): Show | 4 | HG02109.hp2 HG02647.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-15251T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6998790 | ||||||
| chr12:6999256
|
C | G | 28 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(25): Show | 30 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.152-15717G>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999256 | ||||||
| chr12:6999380
|
A | T | 1 | a0002c0002t0007g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.152-15841T>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999380 | ||||||
| chr12:6999395
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-15856C>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999395 | ||||||
| chr12:6999582
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152-16043C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999582 | ||||||
| chr12:6999868
|
T | G | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-16329A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999868 | ||||||
| chr12:6999916
|
C | CT | 35 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0034others(32): Show | 37 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.152-16378dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999916 | ||||||
| chr12:6999916
|
C | CTT | 10 | a0002c0002t0001g0255a0002c0002t0010g0267a0002c0003t0001g0079others(7): Show | 10 | HG00323.hp1 HG01069.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-16379_152-1637 others(6): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999916 | ||||||
| chr12:6999916
|
C | CTTT | 15 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(12): Show | 15 | HG00423.hp2 HG00642.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-16380_152-1637 others(7): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999916 | ||||||
| chr12:6999916
|
CT | C | 15 | a0001c0001t0001g0058a0001c0001t0001g0112a0001c0001t0001g0174others(12): Show | 15 | HG00673.hp1 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.152-16378delA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999916 | ||||||
| chr12:6999954
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.152-16415G>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999954 | ||||||
| chr12:6999977
|
T | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(49): Show | 54 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.152-16438A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999977 | ||||||
| chr12:7000353
|
C | T | 18 | a0002c0004t0001g0218a0002c0004t0001g0219a0002c0004t0001g0227others(15): Show | 22 | HG02258.hp1 HG02622.hp2 HG02965.hp1 others(19): Show |
intron_variant | MODIFIER | c.152-16814G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7000353 | ||||||
| chr12:7000544
|
C | T | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152-17005G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7000544 | ||||||
| chr12:7000550
|
T | C | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-17011A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7000550 | ||||||
| chr12:7000576
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.152-17037T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7000576 | ||||||
| chr12:7000587
|
C | CA | 69 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(66): Show | 70 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.152-17049dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7000587 | ||||||
| chr12:7000587
|
C | CAA | 21 | a0002c0002t0001g0245a0002c0002t0001g0246a0002c0002t0001g0248others(18): Show | 23 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.152-17050_152-1704 others(6): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7000587 | ||||||
| chr12:7001053
|
G | C | 9 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0262others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+17221C>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7001053 | ||||||
| chr12:7001142
|
A | G | 2 | a0002c0007t0001g0002a0002c0007t0001g0011 | 4 | HG02559.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+17132T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7001142 | ||||||
| chr12:7001225
|
C | G | 3 | a0002c0004t0001g0218a0002c0004t0001g0219a0002c0004t0001g0227 | 3 | HG02622.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.151+17049G>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7001225 | ||||||
| chr12:7001303
|
A | C | 1 | a0002c0002t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.151+16971T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7001303 | ||||||
| chr12:7001547
|
C | T | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151+16727G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7001547 | ||||||
| chr12:7001548
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.151+16726C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7001548 | ||||||
| chr12:7001626
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.151+16648C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7001626 | ||||||
| chr12:7001631
|
C | T | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151+16643G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7001631 | ||||||
| chr12:7002134
|
C | T | 8 | a0002c0003t0001g0024a0002c0003t0001g0079a0002c0003t0001g0086others(5): Show | 8 | HG00423.hp2 HG01069.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+16140G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7002134 | ||||||
| chr12:7002472
|
A | C | 1 | a0002c0002t0001g0246 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.151+15802T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7002472 | ||||||
| chr12:7002495
|
T | TG | 9 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0262others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+15778_151+1577 others(5): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7002495 | ||||||
| chr12:7002681
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG00609.hp2 NA18947.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.151+15593T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7002681 | ||||||
| chr12:7002736
|
C | T | 1 | a0002c0002t0007g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.151+15538G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7002736 | ||||||
| chr12:7002762
|
G | A | 21 | a0002c0003t0001g0006a0002c0003t0001g0024a0002c0003t0001g0079others(18): Show | 22 | HG00423.hp2 HG01069.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+15512C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7002762 | ||||||
| chr12:7003027
|
T | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0106others(14): Show | 19 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.151+15247A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003027 | ||||||
| chr12:7003030
|
C | A | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+15244G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003030 | ||||||
| chr12:7003266
|
G | A | 84 | a0002c0002t0001g0085a0002c0002t0001g0217a0002c0002t0001g0244others(81): Show | 93 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.151+15008C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003266 | ||||||
| chr12:7003355
|
G | A | 10 | a0002c0002t0001g0245a0002c0002t0001g0246a0002c0002t0001g0247others(7): Show | 10 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+14919C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003355 | ||||||
| chr12:7003359
|
G | GT | 10 | a0001c0012t0001g0160a0002c0004t0002g0005a0002c0004t0002g0026others(7): Show | 12 | HG00280.hp2 HG02258.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+14914dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003359 | ||||||
| chr12:7003359
|
GT | G | 8 | a0001c0001t0001g0133a0002c0002t0001g0240a0002c0002t0001g0244others(5): Show | 8 | HG00642.hp2 HG01358.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+14914delA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003359 | ||||||
| chr12:7003406
|
ATT | A | 13 | a0002c0007t0001g0002a0002c0007t0001g0011a0002c0007t0001g0014others(10): Show | 15 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.151+14866_151+1486 others(6): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003406 | ||||||
| chr12:7003408
|
T | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0065 | 2 | NA19007.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.151+14866A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003408 | ||||||
| chr12:7003465
|
C | T | 1 | a0001c0012t0001g0160 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.151+14809G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003465 | ||||||
| chr12:7003512
|
G | A | 9 | a0003c0005t0001g0013a0003c0005t0001g0016a0003c0005t0001g0017others(6): Show | 9 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+14762C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003512 | ||||||
| chr12:7003632
|
C | A | 1 | a0001c0001t0001g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.151+14642G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003632 | ||||||
| chr12:7003641
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0069 | 2 | HG02071.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.151+14633C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003641 | ||||||
| chr12:7003693
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG00558.hp1 NA19068.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.151+14581G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003693 | ||||||
| chr12:7003757
|
T | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(133): Show | 147 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.151+14517A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003757 | ||||||
| chr12:7003783
|
G | A | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+14491C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003783 | ||||||
| chr12:7003790
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0106others(13): Show | 18 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.151+14484G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003790 | ||||||
| chr12:7003811
|
A | G | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+14463T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003811 | ||||||
| chr12:7003879
|
A | G | 84 | a0002c0002t0001g0085a0002c0002t0001g0217a0002c0002t0001g0244others(81): Show | 93 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.151+14395T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003879 | ||||||
| chr12:7003928
|
C | CA | 68 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0067others(65): Show | 72 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.151+14345dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003928 | ||||||
| chr12:7003928
|
C | CAA | 11 | a0001c0001t0001g0078a0001c0001t0001g0175a0001c0001t0001g0176others(8): Show | 11 | HG01361.hp2 HG02074.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+14344_151+1434 others(6): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003928 | ||||||
| chr12:7003928
|
CA | C | 24 | a0001c0001t0001g0035a0001c0001t0001g0092a0002c0002t0001g0245others(21): Show | 24 | HG00323.hp1 HG00738.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.151+14345delT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003928 | ||||||
| chr12:7004193
|
C | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG00609.hp1 NA18747.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+14081G>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7004193 | ||||||
| chr12:7004320
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.151+13954C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7004320 | ||||||
| chr12:7004368
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.151+13906T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7004368 | ||||||
| chr12:7004915
|
A | AT | 4 | a0001c0001t0001g0034a0002c0002t0001g0264a0002c0002t0001g0268others(1): Show | 4 | HG02622.hp1 HG02922.hp1 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+13358dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7004915 | ||||||
| chr12:7004931
|
A | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0186a0001c0001t0001g0188others(10): Show | 13 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.151+13343T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7004931 | ||||||
| chr12:7004943
|
T | G | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151+13331A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7004943 | ||||||
| chr12:7004967
|
C | T | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+13307G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7004967 | ||||||
| chr12:7005148
|
G | A | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+13126C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7005148 | ||||||
| chr12:7005568
|
G | T | 1 | a0001c0001t0001g0033 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.151+12706C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7005568 | ||||||
| chr12:7005597
|
T | C | 84 | a0002c0002t0001g0085a0002c0002t0001g0217a0002c0002t0001g0244others(81): Show | 93 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.151+12677A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7005597 | ||||||
| chr12:7005654
|
G | GTGGTTTT others(4): Show |
1 | a0001c0001t0001g0204 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.151+12609_151+1261 others(15): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7005654 | ||||||
| chr12:7005727
|
T | C | 11 | a0002c0004t0002g0001a0002c0004t0002g0220a0002c0004t0002g0221others(8): Show | 14 | NA18941.hp2 NA18942.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.151+12547A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7005727 | ||||||
| chr12:7006170
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.151+12104G>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006170 | ||||||
| chr12:7006171
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.151+12103C>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006171 | ||||||
| chr12:7006451
|
T | C | 5 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+11823A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006451 | ||||||
| chr12:7006461
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.151+11813G>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006461 | ||||||
| chr12:7006462
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.151+11812C>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006462 | ||||||
| chr12:7006492
|
T | C | 11 | a0001c0001t0001g0070a0002c0002t0001g0245a0002c0002t0001g0246others(8): Show | 11 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+11782A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006492 | ||||||
| chr12:7006497
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.151+11777C>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006497 | ||||||
| chr12:7006498
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.151+11776G>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006498 | ||||||
| chr12:7006589
|
T | C | 3 | a0002c0004t0001g0218a0002c0004t0001g0219a0002c0004t0001g0227 | 3 | HG02622.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.151+11685A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006589 | ||||||
| chr12:7006604
|
A | T | 1 | a0002c0003t0001g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.151+11670T>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006604 | ||||||
| chr12:7006671
|
C | T | 41 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(38): Show | 44 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.151+11603G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006671 | ||||||
| chr12:7006769
|
T | G | 62 | a0002c0002t0001g0085a0002c0002t0001g0217a0002c0002t0001g0244others(59): Show | 69 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.151+11505A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006769 | ||||||
| chr12:7006816
|
T | C | 1 | a0002c0003t0001g0007 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.151+11458A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006816 | ||||||
| chr12:7006861
|
A | C | 1 | a0002c0002t0001g0263 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.151+11413T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006861 | ||||||
| chr12:7006891
|
C | T | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+11383G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006891 | ||||||
| chr12:7007065
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.151+11209G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007065 | ||||||
| chr12:7007104
|
C | T | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+11170G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007104 | ||||||
| chr12:7007137
|
G | A | 1 | a0002c0003t0001g0007 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.151+11137C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007137 | ||||||
| chr12:7007278
|
T | C | 11 | a0002c0004t0002g0001a0002c0004t0002g0220a0002c0004t0002g0221others(8): Show | 14 | NA18941.hp2 NA18942.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.151+10996A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007278 | ||||||
| chr12:7007282
|
C | A | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151+10992G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007282 | ||||||
| chr12:7007300
|
C | A | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+10974G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007300 | ||||||
| chr12:7007301
|
T | C | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+10973A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007301 | ||||||
| chr12:7007343
|
G | A | 4 | a0002c0004t0002g0005a0002c0004t0002g0026a0002c0004t0002g0081others(1): Show | 5 | HG02258.hp1 HG02965.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+10931C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007343 | ||||||
| chr12:7007368
|
CT | C | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+10905delA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007368 | ||||||
| chr12:7007450
|
A | ACAT | 6 | a0002c0003t0001g0006a0002c0003t0001g0125a0002c0003t0001g0126others(3): Show | 7 | HG02451.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.151+10821_151+1082 others(7): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007450 | ||||||
| chr12:7007493
|
C | CT | 36 | a0001c0001t0001g0032a0001c0001t0001g0105a0001c0001t0001g0108others(33): Show | 37 | HG00323.hp1 HG00642.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.151+10780dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007493 | ||||||
| chr12:7007493
|
C | CTT | 11 | a0002c0002t0001g0245a0002c0002t0001g0246a0002c0002t0001g0247others(8): Show | 11 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+10779_151+1078 others(6): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007493 | ||||||
| chr12:7007493
|
CT | C | 15 | a0001c0001t0001g0071a0001c0001t0001g0183a0002c0004t0001g0227others(12): Show | 17 | HG01169.hp1 HG01192.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+10780delA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007493 | ||||||
| chr12:7007494
|
T | C | 1 | a0002c0003t0001g0007 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.151+10780A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007494 | ||||||
| chr12:7007500
|
T | G | 1 | a0002c0003t0001g0007 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.151+10774A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007500 | ||||||
| chr12:7007550
|
A | G | 3 | a0002c0003t0001g0122a0002c0003t0001g0234a0002c0003t0001g0235 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151+10724T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007550 | ||||||
| chr12:7007640
|
G | T | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+10634C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007640 | ||||||
| chr12:7007791
|
G | A | 2 | a0002c0004t0002g0238a0002c0004t0002g0239 | 2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.151+10483C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007791 | ||||||
| chr12:7007819
|
T | A | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+10455A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007819 | ||||||
| chr12:7007953
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.151+10321T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007953 | ||||||
| chr12:7008144
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.151+10130A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7008144 | ||||||
| chr12:7008569
|
G | T | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+9705C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7008569 | ||||||
| chr12:7008751
|
C | CA | 6 | a0001c0001t0001g0104a0004c0006t0003g0010a0004c0006t0003g0256others(3): Show | 7 | HG03831.hp1 HG03831.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.151+9522dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7008751 | ||||||
| chr12:7009229
|
T | C | 1 | a0003c0005t0001g0022 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.151+9045A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7009229 | ||||||
| chr12:7009312
|
C | T | 13 | a0002c0003t0001g0006a0002c0003t0001g0122a0002c0003t0001g0123others(10): Show | 14 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.151+8962G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7009312 | ||||||
| chr12:7009340
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+8934G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7009340 | ||||||
| chr12:7009352
|
C | T | 1 | a0002c0003t0001g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.151+8922G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7009352 | ||||||
| chr12:7009676
|
G | A | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+8598C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7009676 | ||||||
| chr12:7009702
|
T | C | 9 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0262others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+8572A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7009702 | ||||||
| chr12:7009902
|
A | T | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+8372T>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7009902 | ||||||
| chr12:7009956
|
A | C | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+8318T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7009956 | ||||||
| chr12:7010043
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.151+8231A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7010043 | ||||||
| chr12:7010416
|
T | A | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+7858A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7010416 | ||||||
| chr12:7010768
|
T | G | 1 | a0001c0001t0009g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.151+7506A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7010768 | ||||||
| chr12:7011014
|
A | G | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+7260T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011014 | ||||||
| chr12:7011052
|
T | G | 41 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(38): Show | 44 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.151+7222A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011052 | ||||||
| chr12:7011104
|
G | A | 19 | a0001c0001t0001g0029a0001c0001t0001g0083a0001c0001t0001g0186others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.151+7170C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011104 | ||||||
| chr12:7011116
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.151+7158C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011116 | ||||||
| chr12:7011385
|
C | A | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+6889G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011385 | ||||||
| chr12:7011584
|
G | A | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151+6690C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011584 | ||||||
| chr12:7011647
|
C | CA | 6 | a0001c0001t0001g0073a0001c0001t0001g0105a0001c0001t0001g0184others(3): Show | 6 | HG03516.hp2 HG04115.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+6626dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011647 | ||||||
| chr12:7011647
|
CA | C | 39 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0074others(36): Show | 41 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.151+6626delT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011647 | ||||||
| chr12:7011647
|
CAA | C | 18 | a0002c0003t0001g0122a0002c0003t0001g0123a0002c0003t0001g0234others(15): Show | 20 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.151+6625_151+6626d others(4): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011647 | ||||||
| chr12:7011664
|
AAAAAG | A | 10 | a0002c0002t0001g0245a0002c0002t0001g0246a0002c0002t0001g0247others(7): Show | 10 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+6605_151+6609d others(7): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011664 | ||||||
| chr12:7012104
|
C | A | 1 | a0002c0002t0001g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151+6170G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7012104 | ||||||
| chr12:7012129
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.151+6145G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7012129 | ||||||
| chr12:7012357
|
C | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.151+5917G>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7012357 | ||||||
| chr12:7012383
|
C | CTTTAAGA others(3): Show |
136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(133): Show | 147 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.151+5890_151+5891i others(12): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7012383 | ||||||
| chr12:7012478
|
G | A | 19 | a0001c0001t0001g0029a0001c0001t0001g0083a0001c0001t0001g0186others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.151+5796C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7012478 | ||||||
| chr12:7012760
|
A | G | 18 | a0001c0001t0001g0027a0001c0001t0001g0108a0001c0001t0001g0109others(15): Show | 18 | HG00544.hp1 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.151+5514T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7012760 | ||||||
| chr12:7012896
|
C | T | 1 | a0006c0010t0001g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.151+5378G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7012896 | ||||||
| chr12:7012969
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.151+5305A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7012969 | ||||||
| chr12:7013000
|
G | A | 12 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(9): Show | 12 | HG00423.hp1 HG00609.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+5274C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013000 | ||||||
| chr12:7013059
|
A | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.151+5215T>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013059 | ||||||
| chr12:7013092
|
G | A | 251 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(248): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.151+5182C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013092 | ||||||
| chr12:7013109
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.151+5165C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013109 | ||||||
| chr12:7013189
|
G | T | 8 | a0002c0003t0001g0024a0002c0003t0001g0079a0002c0003t0001g0086others(5): Show | 8 | HG00423.hp2 HG01069.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+5085C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013189 | ||||||
| chr12:7013513
|
A | G | 14 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+4761T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013513 | ||||||
| chr12:7013532
|
C | T | 44 | a0002c0002t0001g0085a0002c0002t0001g0217a0002c0002t0001g0244others(41): Show | 47 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.151+4742G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013532 | ||||||
| chr12:7013638
|
T | C | 62 | a0002c0002t0001g0085a0002c0002t0001g0217a0002c0002t0001g0244others(59): Show | 69 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.151+4636A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013638 | ||||||
| chr12:7013654
|
A | G | 1 | a0002c0002t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.151+4620T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013654 | ||||||
| chr12:7013942
|
CA | C | 13 | a0002c0007t0001g0002a0002c0007t0001g0011a0002c0007t0001g0014others(10): Show | 15 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.151+4331delT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013942 | ||||||
| chr12:7014074
|
A | G | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+4200T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014074 | ||||||
| chr12:7014468
|
C | T | 4 | a0002c0007t0001g0002a0002c0007t0001g0011a0002c0007t0001g0014others(1): Show | 6 | HG02559.hp2 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+3806G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014468 | ||||||
| chr12:7014529
|
A | G | 3 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0262 | 3 | HG02809.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.151+3745T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014529 | ||||||
| chr12:7014764
|
G | A | 1 | a0002c0002t0007g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.151+3510C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014764 | ||||||
| chr12:7014841
|
C | T | 2 | a0001c0001t0001g0229a0002c0007t0001g0014 | 2 | HG03579.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.151+3433G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014841 | ||||||
| chr12:7014848
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.151+3426C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014848 | ||||||
| chr12:7014883
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.151+3391T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014883 | ||||||
| chr12:7014892
|
C | CA | 13 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(10): Show | 13 | HG00558.hp2 HG01175.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.151+3381dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014892 | ||||||
| chr12:7014892
|
C | CAAAAAAA others(1): Show |
9 | a0002c0002t0001g0246a0002c0002t0001g0247a0002c0002t0001g0248others(6): Show | 9 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+3374_151+3381d others(10): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014892 | ||||||
| chr12:7014892
|
C | CAAAAAAA others(3): Show |
4 | a0002c0002t0001g0244a0002c0002t0001g0255a0002c0002t0004g0242others(1): Show | 4 | HG00323.hp1 HG00642.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3372_151+3381d others(12): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014892 | ||||||
| chr12:7014892
|
CA | C | 12 | a0001c0001t0001g0080a0001c0001t0001g0083a0002c0002t0001g0260others(9): Show | 14 | HG01069.hp2 HG01168.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+3381delT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7014892 | ||||||
| chr12:7015109
|
G | T | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+3165C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7015109 | ||||||
| chr12:7015112
|
T | A | 1 | a0002c0004t0002g0239 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+3162A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7015112 | ||||||
| chr12:7015270
|
T | C | 5 | a0004c0006t0003g0010a0004c0006t0003g0256a0004c0006t0003g0257others(2): Show | 6 | HG03831.hp1 HG04115.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+3004A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7015270 | ||||||
| chr12:7015322
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02074.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.151+2952T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7015322 | ||||||
| chr12:7015772
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(49): Show | 54 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.151+2502G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7015772 | ||||||
| chr12:7016277
|
A | AT | 6 | a0001c0001t0001g0029a0002c0002t0001g0244a0002c0002t0004g0242others(3): Show | 6 | HG00642.hp1 HG00642.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+1996dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7016277 | ||||||
| chr12:7016324
|
T | A | 1 | a0002c0002t0001g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.151+1950A>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7016324 | ||||||
| chr12:7016656
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.151+1618G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7016656 | ||||||
| chr12:7016682
|
C | CTGTCAAA others(5): Show |
1 | a0001c0001t0001g0241 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.151+1580_151+1591d others(14): Show |
LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7016682 | ||||||
| chr12:7016823
|
G | T | 1 | a0001c0001t0001g0027 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.151+1451C>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7016823 | ||||||
| chr12:7017043
|
A | G | 41 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(38): Show | 44 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.151+1231T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7017043 | ||||||
| chr12:7017127
|
A | G | 1 | a0002c0004t0002g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.151+1147T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7017127 | ||||||
| chr12:7017218
|
T | C | 41 | a0002c0002t0001g0244a0002c0002t0001g0245a0002c0002t0001g0246others(38): Show | 44 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.151+1056A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7017218 | ||||||
| chr12:7017223
|
C | T | 2 | a0002c0007t0001g0002a0002c0007t0001g0011 | 4 | HG02559.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+1051G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7017223 | ||||||
| chr12:7017499
|
A | G | 1 | a0002c0002t0007g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.151+775T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7017499 | ||||||
| chr12:7017583
|
C | T | 1 | a0002c0003t0001g0024 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.151+691G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7017583 | ||||||
| chr12:7017619
|
T | C | 9 | a0002c0002t0001g0260a0002c0002t0001g0261a0002c0002t0001g0262others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+655A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7017619 | ||||||
| chr12:7018110
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+164T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7018110 | ||||||
| chr12:7018115
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.151+159A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7018115 |