Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MASSA others(482): Show |
chr12 | 6971185 | 7023476 |
| a0002 | 0/0 | 487 | 78 | 51 | 7 | 17 | 1 | 2 | 14 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | MASSA others(482): Show |
chr12 | 6971185 | 7023476 |
| a0003 | 0/1 | 487 | 9 | 2 | 1 | 2 | 0 | 3 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | MASSA others(482): Show |
chr12 | 6971185 | 7023476 |
| a0004 | 0/0 | 487 | 6 | 0 | 0 | 4 | 0 | 2 | 4 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | MASSA others(482): Show |
chr12 | 6971185 | 7023476 |
| a0005 | 0/0 | 487 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | MASSA others(482): Show |
chr12 | 6971185 | 7023476 |
| a0006 | 0/0 | 487 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | MASSA others(482): Show |
chr12 | 6971185 | 7023476 |
| a0007 | 0/0 | 487 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | MASSA others(482): Show |
chr12 | 6971185 | 7023476 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1461 | 184 | 34 | 36 | 90 | 6 | 17 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0001c0012 | 0/0 | 1461 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0002c0002 | 0/0 | 1461 | 27 | 22 | 4 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0002c0003 | 0/0 | 1461 | 24 | 16 | 3 | 3 | 0 | 2 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0002c0004 | 0/0 | 1461 | 22 | 8 | 0 | 14 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0002c0007 | 0/0 | 1461 | 5 | 5 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0003c0005 | 0/1 | 1461 | 8 | 2 | 1 | 1 | 0 | 3 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0003c0009 | 0/0 | 1461 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0004c0006 | 0/0 | 1461 | 6 | 0 | 0 | 4 | 0 | 2 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0005c0008 | 0/0 | 1461 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0006c0010 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
chr12 | 6971185 | 7023476 | ||
| a0007c0011 | 0/0 | 1461 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | ATGGC others(1456): Show |
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 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0001c0001t0006 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0001c0001t0008 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0001c0001t0009 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0001c0001t0011 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0001c0012t0001 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0002c0002t0001 | 0/0 | 2235 | 23 | 18 | 4 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0002c0002t0004 | 0/0 | 2235 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0002c0002t0007 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0002c0002t0010 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0002c0003t0001 | 0/0 | 2235 | 24 | 16 | 3 | 3 | 0 | 2 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0002c0004t0001 | 0/0 | 2235 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0002c0004t0002 | 0/0 | 2235 | 19 | 5 | 0 | 14 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0002c0007t0001 | 0/0 | 2235 | 5 | 5 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0003c0005t0001 | 0/1 | 2235 | 8 | 2 | 1 | 1 | 0 | 3 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0003c0009t0001 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0004c0006t0003 | 0/0 | 2235 | 5 | 0 | 0 | 4 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0004c0006t0005 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0005c0008t0001 | 0/0 | 2235 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0006c0010t0001 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| a0007c0011t0001 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | GCATT others(2230): Show |
chr12 | 6971185 | 7023476 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 1 | 3 | 3 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0131 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0193 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0009g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0001t0011g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0001c0012t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0239 | 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 |
| a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0002t0010g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0007t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0002c0007t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0005t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0003c0009t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0004c0006t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0004c0006t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0004c0006t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0004c0006t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0004c0006t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0005c0008t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0005c0008t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0006c0010t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| a0007c0011t0001g0104 | 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 | g0171 | EUR | GBR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00280 | hp2 | a0001 | c0012 | t0001 | g0148 | EUR | FIN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0231 | EUR | FIN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0034 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0074 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01175 | hp1 | a0001 | c0001 | t0009 | g0173 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01192 | hp2 | a0003 | c0005 | t0001 | g0028 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | 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 | g0018 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0112 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0242 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01891 | hp2 | a0003 | c0005 | t0001 | g0029 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0085 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0083 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02015 | hp1 | a0005 | c0008 | t0001 | g0097 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02040 | hp2 | a0005 | c0008 | t0001 | g0088 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02056 | hp1 | a0003 | c0009 | t0001 | g0022 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0082 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02129 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02135 | hp2 | a0003 | c0005 | t0001 | g0023 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0128 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02258 | hp1 | a0002 | c0004 | t0002 | g0076 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0111 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0118 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02602 | hp1 | a0003 | c0005 | t0001 | g0030 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02622 | hp2 | a0002 | c0004 | t0001 | g0196 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0116 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0221 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02818 | hp1 | a0002 | c0007 | t0001 | g0005 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0216 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0110 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0211 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0210 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0244 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0117 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02965 | hp1 | a0002 | c0004 | t0002 | g0008 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02976 | hp1 | a0006 | c0010 | t0001 | g0025 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0203 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03017 | hp2 | a0002 | c0003 | t0001 | g0080 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03139 | hp1 | a0003 | c0005 | t0001 | g0032 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0115 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0114 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0195 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03453 | hp2 | a0002 | c0002 | t0004 | g0218 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03486 | hp1 | a0002 | c0004 | t0002 | g0008 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03486 | hp2 | a0002 | c0007 | t0001 | g0005 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | ESN | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03540 | hp2 | a0002 | c0002 | t0004 | g0219 | AFR | GWD | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03579 | hp1 | a0002 | c0007 | t0001 | g0024 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03688 | hp2 | a0003 | c0005 | t0001 | g0027 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03831 | hp1 | a0004 | c0006 | t0003 | g0232 | SAS | BEB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04115 | hp2 | a0004 | c0006 | t0005 | g0235 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | 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 | g0026 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG04228 | hp2 | a0002 | c0003 | t0001 | g0084 | SAS | STU | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18522 | hp1 | a0002 | c0004 | t0002 | g0036 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0223 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18941 | hp2 | a0002 | c0004 | t0002 | g0204 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18942 | hp2 | a0002 | c0004 | t0002 | g0002 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0072 | 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 | g0010 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18950 | hp1 | a0002 | c0004 | t0002 | g0002 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18952 | hp2 | a0002 | c0004 | t0002 | g0002 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18981 | hp1 | a0002 | c0004 | t0002 | g0002 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18999 | hp1 | a0002 | c0004 | t0002 | g0201 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19009 | hp2 | a0002 | c0004 | t0002 | g0200 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19011 | hp1 | a0002 | c0004 | t0002 | g0002 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19011 | hp2 | a0004 | c0006 | t0003 | g0233 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19030 | hp2 | a0002 | c0002 | t0010 | g0243 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19059 | hp1 | a0002 | c0004 | t0002 | g0215 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19072 | hp2 | a0002 | c0004 | t0002 | g0198 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19074 | hp2 | a0004 | c0006 | t0003 | g0020 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19076 | hp1 | a0004 | c0006 | t0003 | g0234 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19076 | hp2 | a0007 | c0011 | t0001 | g0104 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19078 | hp2 | a0002 | c0004 | t0002 | g0197 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19085 | hp1 | a0004 | c0006 | t0003 | g0020 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19089 | hp2 | a0002 | c0004 | t0002 | g0214 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19090 | hp1 | a0002 | c0004 | t0002 | g0199 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19091 | hp1 | a0002 | c0004 | t0002 | g0202 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0225 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA19240 | hp2 | a0002 | c0004 | t0002 | g0008 | AFR | YRI | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | GIH | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA20905 | hp2 | a0001 | c0001 | t0011 | g0089 | SAS | GIH | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG02559 | hp2 | a0002 | c0007 | t0001 | g0005 | AFR | ACB | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0119 | AFR | MSL | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG06807 | hp1 | a0002 | c0002 | t0007 | g0035 | AFR | USA | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0055 | AFR | USA | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0113 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| NA21309 | hp2 | a0002 | c0007 | t0001 | g0021 | AFR | LWK | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| homoSapiens | chm13v2 | a0003 | c0005 | t0001 | g0031 | REF | REF | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0090 | REF | REF | LPCAT3_chr12_6971185_7023476 | LPCAT3 | chr12 | 6971185 | 7023476 |
| view | 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 | a0002 a0003 a0004 others(1): Show |
93 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(90): 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 | 8 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(5): 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 |
| view | 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 | a0002c0002 a0002c0004 a0002c0007 others(4): Show |
69 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(66): 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 | a0002c0007 a0003c0005 a0003c0009 others(1): Show |
14 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(11): 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 |
| view | 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 | a0004c0006t0003 a0004c0006t0005 |
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 |
| view | 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 | 3 | a0002c0004t0002g0008 a0002c0004t0002g0036 a0002c0004t0002g0076 |
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 | 13 | a0002c0004t0002g0002 a0002c0004t0002g0008 a0002c0004t0002g0036 others(10): 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 | a0002c0003t0001g0082 | 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 | a0001c0001t0001g0178 | 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 | 18 | a0002c0002t0001g0079 a0002c0002t0007g0035 a0002c0004t0001g0195 others(15): 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 | 83 | a0001c0001t0001g0169 a0002c0002t0001g0079 a0002c0002t0001g0194 others(80): Show |
94 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.874-42A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 8/12 | chr12 | 6978549 | |||||||
| chr12:6978748 | G | GCA | 9 | a0002c0003t0001g0082 a0003c0005t0001g0023 a0003c0005t0001g0026 others(6): Show |
9 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(6): 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 | a0001c0001t0001g0093 a0005c0008t0001g0088 a0005c0008t0001g0097 |
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 | 3 | a0001c0001t0001g0019 a0001c0001t0001g0107 a0001c0001t0001g0188 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0245 |
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 | a0007c0011t0001g0104 | 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 | a0001c0001t0001g0190 | 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 | a0002c0004t0001g0195 a0002c0004t0001g0196 a0002c0004t0001g0203 |
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 | a0002c0002t0001g0079 | 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 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 others(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 | 66 | a0001c0001t0001g0050 a0001c0001t0001g0069 a0001c0001t0001g0099 others(63): Show |
73 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.678-443dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980021 | |||||||
| chr12:6980021 | C | CTT | 20 | a0001c0001t0001g0046 a0002c0002t0001g0079 a0002c0002t0001g0216 others(17): 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 | a0001c0001t0001g0044 a0001c0001t0001g0070 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0059 | 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 | a0002c0002t0001g0222 | 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 | 60 | a0002c0002t0001g0079 a0002c0002t0001g0194 a0002c0002t0001g0216 others(57): Show |
69 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.677+553T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 6/12 | chr12 | 6980451 | |||||||
| chr12:6980548 | GTC | G | 10 | a0002c0004t0002g0002 a0002c0004t0002g0197 a0002c0004t0002g0198 others(7): 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 | a0002c0002t0007g0035 | 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 | a0002c0007t0001g0005 a0002c0007t0001g0021 |
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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0002c0002t0001g0216 a0002c0002t0001g0239 a0002c0002t0001g0240 others(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 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 others(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 | 26 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(23): 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 | a0002c0002t0001g0216 a0002c0002t0001g0236 a0002c0002t0001g0237 others(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 | a0001c0001t0001g0126 | 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 | a0002c0007t0001g0021 | 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 | a0001c0001t0001g0144 | 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 | a0007c0011t0001g0104 | 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 | a0002c0002t0001g0216 a0002c0002t0001g0239 a0002c0002t0001g0240 others(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 | a0001c0001t0001g0078 | 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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0002c0003t0001g0111 | 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 | a0007c0011t0001g0104 | 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 | a0007c0011t0001g0104 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0096 | 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 | a0002c0002t0001g0079 | 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 | a0002c0002t0001g0216 a0002c0002t0001g0239 a0002c0002t0001g0240 others(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 | a0002c0002t0001g0194 | 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 | 2 | a0001c0001t0001g0019 a0001c0001t0001g0107 |
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 | a0002c0002t0001g0216 a0002c0002t0001g0236 a0002c0002t0001g0237 others(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 | a0002c0002t0001g0079 | 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0176 | 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 | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.152-1551delT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6985089 | |||||||
| chr12:6985089 | TAA | T | 18 | a0001c0001t0001g0129 a0001c0001t0001g0169 a0002c0002t0001g0220 others(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 | a0002c0002t0001g0225 | 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 | a0001c0001t0001g0095 | 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 | 40 | a0001c0001t0001g0169 a0002c0002t0001g0079 a0002c0002t0001g0194 others(37): 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 | a0001c0001t0001g0061 a0001c0001t0001g0064 |
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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0002c0004t0001g0195 a0002c0004t0001g0196 a0002c0004t0001g0203 |
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 | a0002c0004t0001g0195 a0002c0004t0001g0196 a0002c0004t0001g0203 |
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 | 26 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0078 others(23): 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 | a0002c0004t0002g0214 | 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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0001c0001t0001g0184 | 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 | a0002c0002t0001g0194 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
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 | 16 | a0002c0004t0001g0195 a0002c0004t0001g0196 a0002c0004t0001g0203 others(13): 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0165 |
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 | a0001c0001t0001g0139 a0001c0001t0001g0141 |
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 | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(48): 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 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0050 others(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 | 14 | a0001c0001t0001g0171 a0002c0002t0007g0035 a0002c0004t0002g0002 others(11): 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 | 12 | a0002c0007t0001g0005 a0002c0007t0001g0021 a0002c0007t0001g0024 others(9): Show |
14 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(11): 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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0001c0001t0001g0054 | 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 | a0002c0002t0001g0194 | 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 | 69 | a0002c0002t0001g0079 a0002c0002t0001g0194 a0002c0002t0001g0220 others(66): Show |
80 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.152-3573dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6987111 | |||||||
| chr12:6987111 | C | CAA | 12 | a0002c0002t0001g0216 a0002c0002t0001g0236 a0002c0002t0001g0237 others(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 | a0001c0001t0001g0109 | 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 | a0002c0002t0010g0243 | 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 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
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 | 10 | a0002c0004t0002g0002 a0002c0004t0002g0197 a0002c0004t0002g0198 others(7): 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 | 8 | a0003c0005t0001g0023 a0003c0005t0001g0026 a0003c0005t0001g0027 others(5): Show |
8 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-4806C>T | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6988345 | |||||||
| chr12:6988504 | G | A | 10 | a0002c0004t0002g0002 a0002c0004t0002g0197 a0002c0004t0002g0198 others(7): 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 | a0003c0005t0001g0032 | 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 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 |
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 | a0002c0002t0010g0243 | 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 | a0002c0002t0001g0079 | 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 | 10 | a0002c0004t0002g0002 a0002c0004t0002g0197 a0002c0004t0002g0198 others(7): 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 | a0002c0002t0007g0035 | 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 | a0002c0002t0001g0216 a0002c0002t0001g0236 a0002c0002t0001g0237 others(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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0001c0001t0001g0147 a0001c0001t0001g0167 |
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 | a0005c0008t0001g0088 a0005c0008t0001g0097 |
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 | a0001c0001t0001g0171 | 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 | a0007c0011t0001g0104 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0098 a0001c0001t0001g0108 others(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 | a0007c0011t0001g0104 | 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 | 61 | a0001c0001t0001g0157 a0001c0001t0001g0169 a0002c0002t0001g0079 others(58): Show |
65 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.152-5775delA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6989313 | |||||||
| chr12:6989677 | G | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0153 |
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 | a0002c0004t0002g0215 | 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 | 3 | a0002c0004t0002g0008 a0002c0004t0002g0036 a0002c0004t0002g0076 |
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 | 3 | a0002c0004t0002g0008 a0002c0004t0002g0036 a0002c0004t0002g0076 |
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 | a0001c0001t0001g0154 a0001c0001t0001g0158 |
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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0001c0001t0001g0091 | 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 | a0002c0004t0001g0195 a0002c0004t0001g0196 a0002c0004t0001g0203 |
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 | a0001c0001t0001g0166 | 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 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0192 |
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 | a0001c0001t0001g0144 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0108 | 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 | a0002c0007t0001g0005 a0002c0007t0001g0021 |
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 | a0002c0004t0001g0196 | 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 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 others(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 | 68 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(65): 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 |
7 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0037 others(4): 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 | a0001c0001t0001g0121 a0002c0002t0001g0194 a0002c0002t0001g0220 others(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 | a0001c0001t0009g0173 | 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 | a0002c0007t0001g0005 a0002c0007t0001g0021 |
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 | a0002c0002t0001g0244 | 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 | 10 | a0002c0007t0001g0024 a0003c0005t0001g0023 a0003c0005t0001g0026 others(7): Show |
10 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(7): 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 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0062 others(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 | 28 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(25): 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 | 10 | a0002c0004t0002g0002 a0002c0004t0002g0197 a0002c0004t0002g0198 others(7): 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 | a0002c0007t0001g0005 a0002c0007t0001g0021 |
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 | 55 | a0001c0001t0001g0126 a0001c0001t0001g0189 a0002c0002t0001g0079 others(52): Show |
61 | HG00423.hp2 HG01069.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.152-7378dupT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6990916 | |||||||
| chr12:6990916 | C | CAA | 19 | a0002c0002t0001g0220 a0002c0002t0001g0222 a0002c0002t0001g0231 others(16): 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 | a0002c0002t0001g0221 a0002c0002t0001g0223 a0002c0002t0001g0224 others(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 | a0002c0002t0007g0035 | 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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0002c0002t0001g0216 a0002c0002t0001g0236 a0002c0002t0001g0237 others(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 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 others(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 | 59 | a0002c0002t0001g0079 a0002c0002t0001g0194 a0002c0002t0001g0216 others(56): Show |
68 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(65): 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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0002c0002t0001g0194 | 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 | a0002c0002t0001g0228 | 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 | 39 | a0002c0002t0001g0079 a0002c0002t0001g0194 a0002c0002t0001g0220 others(36): 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 | a0001c0001t0001g0098 | 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 | a0002c0003t0001g0034 | 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 | a0001c0001t0001g0137 | 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 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 |
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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | 3 | a0002c0004t0002g0008 a0002c0004t0002g0036 a0002c0004t0002g0076 |
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 | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(22): 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 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0034 others(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 | a0001c0001t0001g0190 | 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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0001c0001t0001g0069 | 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 | a0002c0002t0001g0244 | 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 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 |
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 | a0002c0002t0001g0194 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0008g0128 | 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 | a0002c0002t0001g0216 a0002c0002t0001g0236 a0002c0002t0001g0237 others(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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0189 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.152-11583delA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6995121 | |||||||
| chr12:6995122 | T | C | 1 | a0002c0004t0002g0215 | 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 | a0002c0003t0001g0110 a0002c0003t0001g0111 a0002c0003t0001g0210 others(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 | a0002c0003t0001g0119 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0057 | 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 | a0002c0002t0001g0220 a0002c0002t0001g0231 a0002c0002t0004g0218 others(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 | a0002c0002t0007g0035 | 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 | a0002c0003t0001g0112 | 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 | a0003c0005t0001g0032 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0134 | 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 | 12 | a0002c0007t0001g0005 a0002c0007t0001g0021 a0002c0007t0001g0024 others(9): Show |
14 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(11): 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 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(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 | 57 | a0002c0002t0001g0194 a0002c0002t0001g0220 a0002c0002t0001g0221 others(54): Show |
66 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.152-13472delT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6997010 | |||||||
| chr12:6997091 | C | T | 1 | a0002c0002t0004g0218 | 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 | a0001c0001t0001g0044 | 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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(48): 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 | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(45): 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0019 a0002c0002t0004g0219 a0002c0004t0002g0199 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0044 a0004c0006t0005g0235 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0002c0002t0001g0079 others(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 | 5 | a0003c0005t0001g0023 a0003c0005t0001g0026 a0003c0005t0001g0027 others(2): Show |
5 | HG01192.hp2 HG02135.hp2 HG03139.hp1 others(2): 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 | a0002c0003t0001g0034 a0002c0003t0001g0074 a0002c0003t0001g0080 others(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 | a0002c0007t0001g0005 a0002c0007t0001g0021 |
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 | a0002c0004t0001g0195 a0002c0004t0001g0196 a0002c0004t0001g0203 |
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 | a0001c0001t0011g0089 | 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 | a0002c0002t0001g0226 a0002c0002t0001g0227 a0002c0002t0001g0229 |
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 | a0002c0002t0001g0222 a0002c0002t0001g0223 a0002c0002t0001g0224 others(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 | a0002c0002t0001g0221 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0213 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0075 a0001c0001t0001g0175 |
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 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0002c0002t0001g0220 |
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 | a0001c0001t0001g0145 | 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 | a0002c0002t0007g0035 | 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 | 9 | a0002c0002t0007g0035 a0002c0004t0002g0002 a0002c0004t0002g0197 others(6): 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 | a0002c0002t0007g0035 | 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 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(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 | 12 | a0002c0007t0001g0005 a0002c0007t0001g0021 a0002c0007t0001g0024 others(9): Show |
14 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(11): 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 | a0002c0004t0002g0202 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0171 | 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 | a0002c0002t0001g0229 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0153 |
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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0001c0001t0001g0124 | 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 | a0002c0002t0001g0223 a0002c0002t0001g0224 a0002c0002t0001g0225 others(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 | 27 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(24): Show |
29 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(26): 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 | a0002c0002t0007g0035 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0092 | 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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | 32 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(29): Show |
36 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.152-16378dupA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 6999916 | |||||||
| chr12:6999916 | C | CTT | 10 | a0002c0002t0001g0231 a0002c0002t0010g0243 a0002c0003t0001g0074 others(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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0106 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0149 | 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 | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(37): 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 | 16 | a0002c0004t0001g0195 a0002c0004t0001g0196 a0002c0004t0001g0203 others(13): 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 | a0002c0002t0001g0194 | 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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0001c0001t0001g0127 | 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 | 65 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0012 others(62): 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 | 20 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0224 others(17): Show |
22 | HG00738.hp2 HG01261.hp1 HG01358.hp1 others(19): 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 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(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 | a0002c0007t0001g0005 a0002c0007t0001g0021 |
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 | a0002c0004t0001g0195 a0002c0004t0001g0196 a0002c0004t0001g0203 |
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 | a0002c0002t0001g0079 | 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 | a0002c0002t0001g0194 | 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 | a0001c0001t0001g0095 | 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 | a0002c0002t0001g0079 | 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 | a0002c0002t0001g0194 | 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 | a0002c0003t0001g0034 a0002c0003t0001g0074 a0002c0003t0001g0080 others(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 | a0002c0002t0001g0222 | 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 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(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 | 2 | a0001c0001t0001g0019 a0001c0001t0001g0186 |
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 | a0002c0002t0007g0035 | 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 | a0002c0003t0001g0014 a0002c0003t0001g0034 a0002c0003t0001g0074 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0100 others(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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | 81 | a0002c0002t0001g0079 a0002c0002t0001g0194 a0002c0002t0001g0220 others(78): Show |
92 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(89): 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 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 others(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 | 9 | a0001c0012t0001g0148 a0002c0004t0002g0008 a0002c0004t0002g0036 others(6): 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 | a0001c0001t0001g0121 a0002c0002t0001g0216 a0002c0002t0001g0220 others(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 | 12 | a0002c0007t0001g0005 a0002c0007t0001g0021 a0002c0007t0001g0024 others(9): Show |
14 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(11): 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 | a0001c0001t0001g0001 a0001c0001t0001g0044 |
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 | a0001c0012t0001g0148 | 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 | 8 | a0003c0005t0001g0023 a0003c0005t0001g0026 a0003c0005t0001g0027 others(5): Show |
8 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(5): 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0061 a0001c0001t0001g0064 |
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 | a0001c0001t0001g0147 a0001c0001t0001g0166 a0001c0001t0001g0167 |
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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(118): Show |
146 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(143): 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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0100 others(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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | 81 | a0002c0002t0001g0079 a0002c0002t0001g0194 a0002c0002t0001g0220 others(78): Show |
92 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.151+14395T>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7003879 | |||||||
| chr12:7003928 | C | CA | 61 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(58): 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 | 10 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0001g0159 others(7): 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 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0002c0002t0001g0221 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0044 a0002c0002t0001g0240 a0002c0002t0001g0244 others(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 | 11 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0168 others(8): 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 | a0002c0002t0001g0194 | 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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0001c0001t0001g0043 | 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 | 81 | a0002c0002t0001g0079 a0002c0002t0001g0194 a0002c0002t0001g0220 others(78): Show |
92 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(89): 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 | a0001c0001t0001g0183 | 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 | 10 | a0002c0004t0002g0002 a0002c0004t0002g0197 a0002c0004t0002g0198 others(7): 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0065 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0183 | 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 | a0002c0004t0001g0195 a0002c0004t0001g0196 a0002c0004t0001g0203 |
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 | a0002c0003t0001g0111 | 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 | 40 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(37): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.151+11603G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7006671 | |||||||
| chr12:7006769 | T | G | 59 | a0002c0002t0001g0079 a0002c0002t0001g0194 a0002c0002t0001g0220 others(56): Show |
68 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(65): 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 | a0002c0003t0001g0015 | 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 | a0002c0002t0001g0239 | 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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0002c0003t0001g0015 | 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 | 10 | a0002c0004t0002g0002 a0002c0004t0002g0197 a0002c0004t0002g0198 others(7): 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 | a0002c0002t0001g0194 | 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 | a0002c0004t0002g0215 | 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 | a0002c0004t0002g0215 | 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 | 3 | a0002c0004t0002g0008 a0002c0004t0002g0036 a0002c0004t0002g0076 |
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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | a0002c0003t0001g0014 a0002c0003t0001g0113 a0002c0003t0001g0114 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0099 a0001c0001t0001g0102 others(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 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 others(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 | 14 | a0001c0001t0001g0066 a0001c0001t0001g0165 a0002c0004t0001g0203 others(11): Show |
16 | HG01169.hp1 HG01192.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.151+10780delA | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7007493 | |||||||
| chr12:7007494 | T | C | 1 | a0002c0003t0001g0015 | 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 | a0002c0003t0001g0015 | 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 | a0002c0003t0001g0110 a0002c0003t0001g0210 a0002c0003t0001g0211 |
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 | a0002c0004t0002g0215 | 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 | a0002c0004t0002g0214 a0002c0004t0002g0215 |
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 | a0002c0004t0002g0215 | 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0069 | 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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0001c0001t0001g0098 a0004c0006t0003g0020 a0004c0006t0003g0232 others(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 | a0003c0005t0001g0032 | 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 | a0002c0003t0001g0014 a0002c0003t0001g0110 a0002c0003t0001g0111 others(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 | a0001c0001t0001g0122 | 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 | a0002c0003t0001g0081 | 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 | a0002c0004t0002g0215 | 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 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(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 | a0002c0004t0002g0215 | 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 | a0002c0004t0002g0215 | 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 | a0001c0001t0001g0067 | 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 | a0002c0004t0002g0215 | 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 | a0001c0001t0009g0173 | 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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | 40 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(37): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.151+7222A>C | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7011052 | |||||||
| chr12:7011104 | G | A | 17 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0077 others(14): 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 | a0002c0002t0001g0079 | 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 | a0002c0004t0002g0215 | 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 | a0002c0002t0001g0194 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0099 a0001c0001t0001g0166 others(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 | 38 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0069 others(35): 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 | 17 | a0002c0003t0001g0110 a0002c0003t0001g0111 a0002c0003t0001g0210 others(14): Show |
19 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(16): 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 | a0002c0002t0001g0221 a0002c0002t0001g0222 a0002c0002t0001g0223 others(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 | a0002c0002t0001g0194 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
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 |
121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(118): Show |
146 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(143): 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 | 17 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0077 others(14): 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 | 15 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(12): 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 | a0006c0010t0001g0025 | 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 | a0001c0001t0001g0182 | 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 | 11 | a0001c0001t0001g0019 a0001c0001t0001g0183 a0001c0001t0001g0184 others(8): 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 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): 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 | a0001c0001t0001g0193 | 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 | a0002c0003t0001g0034 a0002c0003t0001g0074 a0002c0003t0001g0080 others(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 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(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 | 43 | a0002c0002t0001g0079 a0002c0002t0001g0194 a0002c0002t0001g0220 others(40): Show |
46 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.151+4742G>A | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013532 | |||||||
| chr12:7013638 | T | C | 59 | a0002c0002t0001g0079 a0002c0002t0001g0194 a0002c0002t0001g0220 others(56): Show |
68 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(65): 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 | a0002c0002t0001g0079 | 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 | 12 | a0002c0007t0001g0005 a0002c0007t0001g0021 a0002c0007t0001g0024 others(9): Show |
14 | HG01192.hp2 HG01891.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.151+4331delT | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7013942 | |||||||
| chr12:7014074 | A | G | 5 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0002c0007t0001g0005 a0002c0007t0001g0021 a0002c0007t0001g0024 others(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 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 |
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 | a0002c0002t0007g0035 | 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 | a0001c0001t0001g0205 a0002c0007t0001g0024 |
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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0002c0002t0001g0222 a0002c0002t0001g0223 a0002c0002t0001g0224 others(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 | a0002c0002t0001g0220 a0002c0002t0001g0231 a0002c0002t0004g0218 others(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 | 11 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0002c0002t0001g0236 others(8): 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 | a0002c0004t0002g0215 | 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 | a0002c0004t0002g0215 | 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 | a0004c0006t0003g0020 a0004c0006t0003g0232 a0004c0006t0003g0233 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
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 | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(37): 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 | a0001c0001t0001g0039 a0002c0002t0001g0220 a0002c0002t0004g0218 others(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 | a0002c0002t0001g0216 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0037 | 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 | 40 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(37): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): 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 | a0002c0004t0002g0036 | 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 | 40 | a0002c0002t0001g0220 a0002c0002t0001g0221 a0002c0002t0001g0222 others(37): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): 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 | a0002c0007t0001g0005 a0002c0007t0001g0021 |
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 | a0002c0002t0007g0035 | 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 | a0002c0003t0001g0034 | 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 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0002t0001g0238 others(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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0245 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.151+159A>G | LPCAT3 | ENSG00000111684.11 | transcript | ENST00000261407.9 | protein_coding | 1/12 | chr12 | 7018115 |