Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54947 |
| ensemblid | ENSG00000087253.13 |
| hgncid | 26032 |
| symbol | LPCAT2 |
| name | lysophosphatidylcholine acyltransferase 2 |
| refseq_nuc | NM_017839.5 |
| refseq_prot | NP_060309.2 |
| ensembl_nuc | ENST00000262134.10 |
| ensembl_prot | ENSP00000262134.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 55509072 |
| end | 55586666 |
| strand | + |
| ver | v1.2 |
| region | chr16:55509072-55586666 |
| region5000 | chr16:55504072-55591666 |
| regionname0 | LPCAT2_chr16_55509072_55586666 |
| regionname5000 | LPCAT2_chr16_55504072_55591666 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 544 | 157 | 27 | 35 | 63 | 6 | 25 | 44 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | MSRCA others(539): Show |
chr16 | 55504072 | 55591666 |
| a0002 | 1/0 | 544 | 134 | 50 | 16 | 55 | 6 | 6 | 40 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | MSRCA others(539): Show |
chr16 | 55504072 | 55591666 |
| a0003 | 0/0 | 544 | 15 | 4 | 0 | 8 | 0 | 3 | 6 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | MSRCA others(539): Show |
chr16 | 55504072 | 55591666 |
| a0004 | 0/0 | 544 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | MSRCA others(539): Show |
chr16 | 55504072 | 55591666 |
| a0005 | 0/0 | 544 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | MSRCA others(539): Show |
chr16 | 55504072 | 55591666 |
| a0006 | 0/0 | 544 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | MSRCA others(539): Show |
chr16 | 55504072 | 55591666 |
| a0007 | 0/0 | 544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | MSRCA others(539): Show |
chr16 | 55504072 | 55591666 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 1632 | 126 | 14 | 32 | 50 | 6 | 23 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0001c0003 | 0/0 | 1632 | 30 | 13 | 2 | 13 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0001c0011 | 0/0 | 1632 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0002c0001 | 1/0 | 1632 | 129 | 46 | 16 | 54 | 6 | 6 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0002c0005 | 0/0 | 1632 | 5 | 4 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0003c0004 | 0/0 | 1632 | 10 | 0 | 0 | 7 | 0 | 3 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0003c0006 | 0/0 | 1632 | 4 | 4 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0003c0010 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0004c0007 | 0/0 | 1632 | 4 | 0 | 2 | 0 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0005c0008 | 0/0 | 1632 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0006c0012 | 0/0 | 1632 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 | ||
| a0007c0009 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | ATGAG others(1627): Show |
chr16 | 55504072 | 55591666 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 5313 | 43 | 1 | 19 | 13 | 3 | 6 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0002 | 0/0 | 5309 | 3 | 0 | 0 | 1 | 1 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0003 | 0/0 | 5309 | 4 | 0 | 2 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0004 | 0/0 | 5313 | 18 | 1 | 3 | 11 | 1 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0005 | 0/0 | 5375 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0006 | 0/0 | 5309 | 7 | 1 | 0 | 1 | 1 | 4 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0007 | 0/0 | 5375 | 12 | 1 | 3 | 6 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0008 | 0/0 | 5305 | 3 | 0 | 0 | 0 | 0 | 3 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5300): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0009 | 0/0 | 5313 | 6 | 1 | 2 | 0 | 0 | 3 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0013 | 0/0 | 5313 | 4 | 0 | 0 | 3 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0014 | 0/0 | 5312 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5307): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0016 | 0/0 | 5305 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5300): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0017 | 0/0 | 5375 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0025 | 0/0 | 5309 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0026 | 0/0 | 5313 | 2 | 0 | 2 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0029 | 0/0 | 5309 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0031 | 0/0 | 5313 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0035 | 0/0 | 5371 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5366): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0036 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5366): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0040 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0042 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0043 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0044 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0046 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0001c0002t0050 | 0/0 | 5375 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0010 | 0/0 | 5313 | 6 | 1 | 1 | 3 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0011 | 0/0 | 5313 | 8 | 3 | 0 | 5 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0021 | 0/0 | 5375 | 4 | 3 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0034 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5366): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0037 | 0/0 | 5309 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0038 | 0/0 | 5313 | 2 | 1 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0059 | 0/0 | 5312 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5307): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0060 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0069 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0070 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0071 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0001c0003t0072 | 0/0 | 5375 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0001c0011t0001 | 0/0 | 5313 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0002 | 0/0 | 5309 | 17 | 3 | 4 | 7 | 2 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0003 | 0/0 | 5309 | 14 | 7 | 2 | 2 | 2 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0005 | 0/0 | 5375 | 16 | 0 | 4 | 11 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0006 | 0/0 | 5309 | 8 | 1 | 1 | 6 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0008 | 0/0 | 5305 | 7 | 4 | 0 | 3 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5300): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0009 | 0/0 | 5313 | 3 | 1 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0012 | 0/0 | 5309 | 7 | 0 | 1 | 6 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0013 | 1/0 | 5313 | 2 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0014 | 0/0 | 5312 | 4 | 4 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5307): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0015 | 0/0 | 5313 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0016 | 0/0 | 5305 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5300): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0018 | 0/0 | 5375 | 4 | 4 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0019 | 0/0 | 5313 | 4 | 1 | 1 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0020 | 0/0 | 5313 | 3 | 0 | 1 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0024 | 0/0 | 5375 | 3 | 1 | 0 | 0 | 2 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0025 | 0/0 | 5309 | 2 | 0 | 1 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0027 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5366): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0028 | 0/0 | 5312 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5307): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0030 | 0/0 | 5313 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0032 | 0/0 | 5313 | 2 | 0 | 0 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0033 | 0/0 | 5375 | 2 | 1 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0035 | 0/0 | 5371 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5366): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0048 | 0/0 | 5375 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0049 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0051 | 0/0 | 5312 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5307): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0052 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0053 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0054 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0055 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0056 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0057 | 0/0 | 5375 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0058 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0061 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0062 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0064 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0065 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5366): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0066 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0067 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5366): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0068 | 0/0 | 5308 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5303): Show |
chr16 | 55504072 | 55591666 |
| a0002c0001t0073 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0002c0005t0010 | 0/0 | 5313 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0005t0011 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0002c0005t0063 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0003c0004t0022 | 0/0 | 5313 | 4 | 0 | 0 | 3 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0003c0004t0039 | 0/0 | 5313 | 2 | 0 | 0 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0003c0004t0045 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0003c0004t0074 | 0/0 | 5313 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0003c0004t0075 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0003c0004t0077 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0003c0006t0023 | 0/0 | 5316 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5311): Show |
chr16 | 55504072 | 55591666 |
| a0003c0006t0047 | 0/0 | 5375 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5370): Show |
chr16 | 55504072 | 55591666 |
| a0003c0010t0076 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0004c0007t0002 | 0/0 | 5309 | 2 | 0 | 1 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0004c0007t0003 | 0/0 | 5309 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0004c0007t0008 | 0/0 | 5305 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5300): Show |
chr16 | 55504072 | 55591666 |
| a0005c0008t0015 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0005c0008t0020 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5308): Show |
chr16 | 55504072 | 55591666 |
| a0006c0012t0041 | 0/0 | 5309 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5304): Show |
chr16 | 55504072 | 55591666 |
| a0007c0009t0014 | 0/0 | 5312 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | AGAGG others(5307): Show |
chr16 | 55504072 | 55591666 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0004 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0006g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0006g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0006g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0007g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0007g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0007g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0007g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0007g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0007g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0007g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0008g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0008g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0009g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0009g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0009g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0009g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0009g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0013g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0013g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0013g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0013g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0016g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0016g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0017g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0017g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0017g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0017g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0025g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0026g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0026g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0029g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0029g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0031g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0031g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0035g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0036g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0040g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0042g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0043g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0044g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0046g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0002t0050g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0010g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0010g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0010g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0010g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0011g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0011g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0011g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0011g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0021g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0021g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0021g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0021g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0034g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0034g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0037g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0037g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0038g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0038g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0059g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0060g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0069g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0070g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0071g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0003t0072g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0001c0011t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0007 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0006g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0006g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0008g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0009g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0009g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0012g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0012g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0012g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0012g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0012g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0012g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0012g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0013g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0014g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0014g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0014g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0015g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0015g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0015g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0016g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0018g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0018g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0018g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0019g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0019g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0019g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0019g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0020g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0020g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0024g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0024g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0025g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0025g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0027g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0028g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0028g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0030g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0032g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0032g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0033g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0033g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0035g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0048g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0049g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0051g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0052g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0053g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0054g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0055g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0056g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0057g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0058g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0061g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0062g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0064g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0065g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0066g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0067g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0068g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0001t0073g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0005t0010g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0005t0010g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0005t0011g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0002c0005t0063g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0004t0022g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0004t0022g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0004t0022g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0004t0039g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0004t0039g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0004t0045g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0004t0074g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0004t0075g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0004t0077g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0006t0023g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0006t0023g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0006t0023g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0006t0047g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0003c0010t0076g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0004c0007t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0004c0007t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0004c0007t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0004c0007t0008g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0005c0008t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0005c0008t0020g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0006c0012t0041g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| a0007c0009t0014g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0008 | EUR | GBR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | GBR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00280 | hp1 | a0002 | c0001 | t0003 | g0007 | EUR | FIN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | FIN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00408 | hp1 | a0001 | c0002 | t0007 | g0009 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00408 | hp2 | a0002 | c0001 | t0006 | g0109 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00438 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00438 | hp2 | a0003 | c0004 | t0039 | g0187 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00558 | hp1 | a0002 | c0001 | t0062 | g0001 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00597 | hp1 | a0001 | c0002 | t0043 | g0226 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00597 | hp2 | a0001 | c0003 | t0037 | g0207 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00609 | hp2 | a0001 | c0003 | t0011 | g0042 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00621 | hp1 | a0001 | c0002 | t0004 | g0009 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00621 | hp2 | a0002 | c0001 | t0002 | g0117 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00639 | hp1 | a0002 | c0001 | t0002 | g0157 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00639 | hp2 | a0001 | c0002 | t0026 | g0050 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00642 | hp1 | a0001 | c0002 | t0007 | g0239 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00733 | hp1 | a0001 | c0003 | t0010 | g0076 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00733 | hp2 | a0001 | c0002 | t0026 | g0225 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00741 | hp1 | a0002 | c0001 | t0003 | g0201 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01069 | hp1 | a0001 | c0002 | t0009 | g0070 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01071 | hp2 | a0001 | c0002 | t0009 | g0067 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01074 | hp1 | a0002 | c0001 | t0003 | g0007 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01099 | hp1 | a0002 | c0001 | t0005 | g0178 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01106 | hp2 | a0002 | c0001 | t0033 | g0143 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01167 | hp2 | a0004 | c0007 | t0002 | g0182 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01168 | hp1 | a0002 | c0001 | t0006 | g0175 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01168 | hp2 | a0001 | c0003 | t0021 | g0056 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01175 | hp2 | a0002 | c0001 | t0005 | g0149 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01192 | hp1 | a0001 | c0002 | t0004 | g0052 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01192 | hp2 | a0002 | c0001 | t0002 | g0200 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01243 | hp1 | a0002 | c0001 | t0020 | g0179 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0204 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01257 | hp2 | a0006 | c0012 | t0041 | g0223 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01261 | hp2 | a0001 | c0002 | t0007 | g0262 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01358 | hp1 | a0001 | c0011 | t0001 | g0264 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01358 | hp2 | a0002 | c0001 | t0002 | g0121 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01361 | hp1 | a0001 | c0002 | t0025 | g0198 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01433 | hp2 | a0004 | c0007 | t0008 | g0181 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01496 | hp1 | a0002 | c0001 | t0005 | g0001 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01515 | hp1 | a0002 | c0001 | t0024 | g0017 | EUR | IBS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01515 | hp2 | a0001 | c0002 | t0006 | g0008 | EUR | IBS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01516 | hp1 | a0002 | c0001 | t0002 | g0016 | EUR | IBS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01516 | hp2 | a0001 | c0002 | t0004 | g0003 | EUR | IBS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01517 | hp1 | a0002 | c0001 | t0002 | g0016 | EUR | IBS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01517 | hp2 | a0002 | c0001 | t0024 | g0017 | EUR | IBS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01891 | hp1 | a0002 | c0001 | t0014 | g0177 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01891 | hp2 | a0001 | c0002 | t0006 | g0082 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01934 | hp1 | a0001 | c0002 | t0004 | g0218 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01934 | hp2 | a0002 | c0001 | t0012 | g0101 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0224 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01952 | hp2 | a0002 | c0001 | t0019 | g0151 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01975 | hp1 | a0002 | c0001 | t0005 | g0154 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02004 | hp1 | a0001 | c0002 | t0007 | g0215 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02004 | hp2 | a0002 | c0001 | t0025 | g0158 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02040 | hp1 | a0001 | c0002 | t0007 | g0009 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02040 | hp2 | a0002 | c0001 | t0064 | g0098 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02055 | hp1 | a0002 | c0001 | t0003 | g0113 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02055 | hp2 | a0001 | c0003 | t0059 | g0079 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02056 | hp1 | a0002 | c0001 | t0006 | g0108 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02071 | hp2 | a0001 | c0003 | t0011 | g0057 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02074 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02074 | hp2 | a0001 | c0003 | t0010 | g0208 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02080 | hp1 | a0001 | c0002 | t0042 | g0227 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02080 | hp2 | a0002 | c0001 | t0012 | g0110 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02083 | hp1 | a0001 | c0003 | t0037 | g0206 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02083 | hp2 | a0002 | c0001 | t0073 | g0162 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02129 | hp1 | a0002 | c0001 | t0015 | g0128 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02132 | hp1 | a0002 | c0001 | t0005 | g0123 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02132 | hp2 | a0002 | c0001 | t0012 | g0028 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02145 | hp1 | a0001 | c0002 | t0014 | g0080 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02145 | hp2 | a0001 | c0003 | t0011 | g0043 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02155 | hp1 | a0002 | c0001 | t0005 | g0085 | EAS | CDX | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02155 | hp2 | a0002 | c0001 | t0008 | g0086 | EAS | CDX | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02165 | hp1 | a0002 | c0001 | t0056 | g0141 | EAS | CDX | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02165 | hp2 | a0002 | c0001 | t0019 | g0140 | EAS | CDX | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02257 | hp1 | a0002 | c0001 | t0003 | g0160 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02257 | hp2 | a0002 | c0005 | t0010 | g0174 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02258 | hp1 | a0002 | c0001 | t0003 | g0172 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02258 | hp2 | a0002 | c0005 | t0063 | g0167 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02280 | hp1 | a0002 | c0001 | t0003 | g0099 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02280 | hp2 | a0002 | c0001 | t0003 | g0126 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02293 | hp1 | a0002 | c0001 | t0002 | g0114 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02293 | hp2 | a0001 | c0002 | t0004 | g0254 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02451 | hp1 | a0001 | c0003 | t0011 | g0030 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02451 | hp2 | a0002 | c0001 | t0053 | g0148 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02572 | hp1 | a0002 | c0001 | t0028 | g0176 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02572 | hp2 | a0003 | c0006 | t0047 | g0012 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02602 | hp1 | a0001 | c0002 | t0035 | g0197 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0253 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02615 | hp1 | a0001 | c0003 | t0034 | g0046 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02615 | hp2 | a0002 | c0001 | t0048 | g0166 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02622 | hp1 | a0002 | c0001 | t0027 | g0014 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02622 | hp2 | a0002 | c0001 | t0014 | g0145 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02647 | hp1 | a0003 | c0006 | t0023 | g0088 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02647 | hp2 | a0002 | c0001 | t0033 | g0092 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0258 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02683 | hp2 | a0001 | c0002 | t0008 | g0026 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0268 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02698 | hp2 | a0002 | c0001 | t0057 | g0129 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02717 | hp1 | a0001 | c0002 | t0016 | g0045 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02717 | hp2 | a0001 | c0003 | t0011 | g0061 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02723 | hp1 | a0002 | c0005 | t0010 | g0021 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02723 | hp2 | a0002 | c0001 | t0018 | g0018 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02735 | hp1 | a0001 | c0002 | t0004 | g0214 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02735 | hp2 | a0004 | c0007 | t0003 | g0184 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0213 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02738 | hp2 | a0001 | c0002 | t0006 | g0199 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02809 | hp1 | a0002 | c0001 | t0030 | g0019 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02809 | hp2 | a0005 | c0008 | t0015 | g0013 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02886 | hp1 | a0002 | c0001 | t0030 | g0019 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02886 | hp2 | a0002 | c0001 | t0009 | g0093 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02896 | hp1 | a0005 | c0008 | t0020 | g0013 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02896 | hp2 | a0001 | c0002 | t0036 | g0011 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02897 | hp1 | a0001 | c0002 | t0036 | g0011 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02897 | hp2 | a0002 | c0001 | t0068 | g0002 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02922 | hp1 | a0001 | c0003 | t0038 | g0065 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02922 | hp2 | a0001 | c0003 | t0034 | g0031 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0217 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02970 | hp2 | a0001 | c0003 | t0060 | g0078 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02976 | hp1 | a0002 | c0001 | t0002 | g0137 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02976 | hp2 | a0002 | c0001 | t0014 | g0094 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03041 | hp1 | a0002 | c0001 | t0018 | g0120 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03041 | hp2 | a0001 | c0003 | t0021 | g0060 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03098 | hp1 | a0001 | c0002 | t0016 | g0081 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03098 | hp2 | a0002 | c0001 | t0003 | g0211 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03130 | hp1 | a0002 | c0001 | t0051 | g0104 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03130 | hp2 | a0001 | c0003 | t0072 | g0210 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03139 | hp1 | a0002 | c0001 | t0065 | g0134 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03139 | hp2 | a0001 | c0002 | t0016 | g0084 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03195 | hp1 | a0002 | c0001 | t0018 | g0020 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03195 | hp2 | a0003 | c0006 | t0023 | g0089 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03209 | hp1 | a0003 | c0006 | t0023 | g0012 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03225 | hp1 | a0002 | c0005 | t0010 | g0021 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03225 | hp2 | a0002 | c0001 | t0027 | g0014 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03453 | hp1 | a0002 | c0001 | t0028 | g0146 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03453 | hp2 | a0002 | c0001 | t0013 | g0029 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03486 | hp1 | a0002 | c0001 | t0018 | g0020 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03486 | hp2 | a0002 | c0001 | t0058 | g0185 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03490 | hp1 | a0001 | c0003 | t0010 | g0077 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03490 | hp2 | a0001 | c0002 | t0006 | g0024 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03491 | hp1 | a0001 | c0002 | t0007 | g0237 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03491 | hp2 | a0003 | c0004 | t0074 | g0188 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03492 | hp1 | a0001 | c0002 | t0006 | g0024 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03492 | hp2 | a0001 | c0002 | t0007 | g0010 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03516 | hp1 | a0002 | c0001 | t0014 | g0095 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03516 | hp2 | a0002 | c0001 | t0016 | g0171 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03579 | hp1 | a0002 | c0001 | t0002 | g0002 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03579 | hp2 | a0001 | c0003 | t0010 | g0063 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03654 | hp1 | a0001 | c0002 | t0008 | g0203 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03654 | hp2 | a0002 | c0001 | t0003 | g0007 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03669 | hp1 | a0001 | c0002 | t0008 | g0026 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03704 | hp1 | a0001 | c0002 | t0006 | g0196 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03704 | hp2 | a0001 | c0002 | t0013 | g0066 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03831 | hp1 | a0001 | c0002 | t0009 | g0069 | SAS | BEB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03831 | hp2 | a0002 | c0001 | t0005 | g0125 | SAS | BEB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | BEB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03927 | hp2 | a0003 | c0004 | t0022 | g0212 | SAS | BEB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03942 | hp1 | a0003 | c0004 | t0039 | g0186 | SAS | BEB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03942 | hp2 | a0001 | c0002 | t0004 | g0259 | SAS | BEB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG04115 | hp1 | a0001 | c0002 | t0009 | g0068 | SAS | STU | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG04115 | hp2 | a0002 | c0001 | t0019 | g0142 | SAS | STU | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG04199 | hp1 | a0004 | c0007 | t0002 | g0183 | SAS | STU | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG04199 | hp2 | a0001 | c0003 | t0038 | g0032 | SAS | STU | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG04228 | hp1 | a0001 | c0002 | t0009 | g0071 | SAS | STU | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG04228 | hp2 | a0002 | c0001 | t0032 | g0136 | SAS | STU | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18747 | hp1 | a0001 | c0003 | t0070 | g0039 | EAS | CHB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18747 | hp2 | a0003 | c0004 | t0077 | g0191 | EAS | CHB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18906 | hp1 | a0002 | c0001 | t0003 | g0156 | AFR | YRI | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18906 | hp2 | a0002 | c0001 | t0006 | g0100 | AFR | YRI | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18939 | hp2 | a0001 | c0002 | t0013 | g0040 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18940 | hp1 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18940 | hp2 | a0001 | c0002 | t0005 | g0202 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18942 | hp1 | a0001 | c0003 | t0010 | g0034 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18942 | hp2 | a0002 | c0001 | t0002 | g0135 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18945 | hp1 | a0002 | c0001 | t0015 | g0001 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0222 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18946 | hp1 | a0002 | c0001 | t0012 | g0102 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18946 | hp2 | a0001 | c0002 | t0007 | g0235 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18949 | hp1 | a0001 | c0002 | t0013 | g0041 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18949 | hp2 | a0001 | c0002 | t0004 | g0027 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18951 | hp1 | a0002 | c0001 | t0025 | g0002 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18951 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18952 | hp2 | a0001 | c0003 | t0011 | g0209 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18953 | hp1 | a0002 | c0001 | t0012 | g0103 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18953 | hp2 | a0001 | c0003 | t0069 | g0195 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18956 | hp2 | a0002 | c0001 | t0005 | g0001 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18957 | hp1 | a0001 | c0002 | t0004 | g0216 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18957 | hp2 | a0002 | c0001 | t0002 | g0161 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18960 | hp1 | a0001 | c0002 | t0046 | g0228 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18960 | hp2 | a0002 | c0001 | t0061 | g0006 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18964 | hp1 | a0002 | c0001 | t0005 | g0150 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18964 | hp2 | a0002 | c0001 | t0049 | g0107 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18965 | hp1 | a0002 | c0001 | t0008 | g0112 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18965 | hp2 | a0001 | c0002 | t0017 | g0243 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18966 | hp1 | a0002 | c0001 | t0005 | g0130 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18966 | hp2 | a0002 | c0001 | t0006 | g0015 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18967 | hp1 | a0002 | c0001 | t0008 | g0002 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18967 | hp2 | a0001 | c0002 | t0017 | g0247 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18968 | hp1 | a0002 | c0001 | t0003 | g0165 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18968 | hp2 | a0003 | c0004 | t0045 | g0022 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18971 | hp1 | a0001 | c0002 | t0005 | g0058 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18971 | hp2 | a0003 | c0004 | t0022 | g0022 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18972 | hp1 | a0001 | c0002 | t0040 | g0234 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18972 | hp2 | a0002 | c0001 | t0035 | g0163 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18973 | hp1 | a0002 | c0001 | t0005 | g0180 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18977 | hp1 | a0002 | c0001 | t0006 | g0111 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18977 | hp2 | a0001 | c0003 | t0071 | g0038 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18978 | hp1 | a0001 | c0002 | t0007 | g0260 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18978 | hp2 | a0001 | c0003 | t0011 | g0059 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18979 | hp1 | a0003 | c0010 | t0076 | g0190 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18979 | hp2 | a0002 | c0001 | t0009 | g0115 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18980 | hp1 | a0002 | c0001 | t0015 | g0131 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18980 | hp2 | a0001 | c0002 | t0029 | g0072 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18981 | hp1 | a0002 | c0001 | t0002 | g0164 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18981 | hp2 | a0001 | c0002 | t0017 | g0219 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18982 | hp2 | a0002 | c0001 | t0066 | g0138 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18989 | hp1 | a0002 | c0001 | t0002 | g0116 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18991 | hp1 | a0001 | c0002 | t0029 | g0055 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18991 | hp2 | a0002 | c0001 | t0015 | g0170 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18992 | hp1 | a0001 | c0002 | t0004 | g0242 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18992 | hp2 | a0002 | c0001 | t0005 | g0001 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18993 | hp1 | a0003 | c0004 | t0075 | g0189 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18993 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18995 | hp1 | a0002 | c0001 | t0005 | g0132 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18995 | hp2 | a0001 | c0002 | t0044 | g0246 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18997 | hp1 | a0003 | c0004 | t0022 | g0023 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18997 | hp2 | a0002 | c0001 | t0002 | g0192 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19000 | hp1 | a0003 | c0004 | t0022 | g0023 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19000 | hp2 | a0002 | c0001 | t0009 | g0118 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19009 | hp1 | a0001 | c0002 | t0004 | g0250 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19009 | hp2 | a0002 | c0001 | t0005 | g0127 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19011 | hp1 | a0002 | c0001 | t0032 | g0152 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19011 | hp2 | a0001 | c0002 | t0013 | g0037 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19030 | hp1 | a0002 | c0001 | t0067 | g0139 | AFR | LWK | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19030 | hp2 | a0002 | c0001 | t0054 | g0144 | AFR | LWK | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19043 | hp1 | a0007 | c0009 | t0014 | g0083 | AFR | LWK | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19043 | hp2 | a0002 | c0001 | t0008 | g0168 | AFR | LWK | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19054 | hp1 | a0002 | c0001 | t0020 | g0006 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19054 | hp2 | a0001 | c0002 | t0007 | g0256 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19059 | hp1 | a0001 | c0002 | t0006 | g0194 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19059 | hp2 | a0002 | c0001 | t0005 | g0087 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19060 | hp1 | a0002 | c0001 | t0005 | g0153 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19060 | hp2 | a0001 | c0002 | t0007 | g0233 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19063 | hp2 | a0002 | c0001 | t0012 | g0106 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19066 | hp1 | a0001 | c0002 | t0017 | g0244 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19066 | hp2 | a0002 | c0001 | t0020 | g0006 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19068 | hp2 | a0002 | c0001 | t0012 | g0105 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19074 | hp1 | a0001 | c0003 | t0011 | g0035 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19074 | hp2 | a0002 | c0001 | t0006 | g0015 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19087 | hp2 | a0002 | c0005 | t0011 | g0133 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19091 | hp1 | a0001 | c0003 | t0010 | g0036 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19091 | hp2 | a0002 | c0001 | t0002 | g0155 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19240 | hp1 | a0001 | c0003 | t0021 | g0064 | AFR | YRI | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA19240 | hp2 | a0002 | c0001 | t0055 | g0018 | AFR | YRI | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA20129 | hp1 | a0001 | c0002 | t0007 | g0010 | AFR | ASW | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA20129 | hp2 | a0002 | c0001 | t0019 | g0091 | AFR | ASW | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0232 | EUR | TSI | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA20752 | hp2 | a0002 | c0001 | t0003 | g0169 | EUR | TSI | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0252 | SAS | GIH | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA20905 | hp2 | a0002 | c0001 | t0002 | g0122 | SAS | GIH | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0205 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02109 | hp1 | a0001 | c0003 | t0021 | g0062 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02109 | hp2 | a0001 | c0002 | t0009 | g0074 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02559 | hp1 | a0002 | c0001 | t0024 | g0090 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG02559 | hp2 | a0002 | c0001 | t0008 | g0173 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03471 | hp1 | a0002 | c0001 | t0002 | g0159 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG03471 | hp2 | a0001 | c0002 | t0031 | g0075 | AFR | MSL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG06807 | hp1 | a0002 | c0001 | t0008 | g0097 | AFR | USA | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| HG06807 | hp2 | a0002 | c0001 | t0052 | g0124 | AFR | USA | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18955 | hp1 | a0002 | c0001 | t0006 | g0119 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA18955 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA20300 | hp1 | a0001 | c0002 | t0031 | g0073 | AFR | USA | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA20300 | hp2 | a0001 | c0002 | t0050 | g0044 | AFR | USA | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA21309 | hp1 | a0002 | c0001 | t0016 | g0193 | AFR | LWK | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| NA21309 | hp2 | a0002 | c0001 | t0008 | g0096 | AFR | LWK | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0048 | REF | REF | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0013 | g0147 | REF | REF | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:55509237 | T | G | 1 | a0007 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.56T>G | p.Val19Gly | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/14 | 166/5313 | 56/1635 | 19/544 | chr16 | 55509237 | |||
| chr16:55509297 | C | T | 1 | a0006 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.116C>T | p.Pro39Leu | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/14 | 226/5313 | 116/1635 | 39/544 | chr16 | 55509297 | |||
| chr16:55525601 | G | A | 1 | a0003 | 4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
missense_variant | MODERATE | c.265G>A | p.Val89Ile | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/14 | 375/5313 | 265/1635 | 89/544 | chr16 | 55525601 | |||
| chr16:55525601 | G | T | 1 | a0003 | 11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
missense_variant | MODERATE | c.265G>T | p.Val89Leu | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/14 | 375/5313 | 265/1635 | 89/544 | chr16 | 55525601 | |||
| chr16:55528447 | G | A | 1 | a0004 | 4 | HG01167.hp2 HG01433.hp2 HG02735.hp2 others(1): Show |
missense_variant | MODERATE | c.382G>A | p.Val128Ile | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/14 | 492/5313 | 382/1635 | 128/544 | chr16 | 55528447 | |||
| chr16:55528554 | G | A | 3 | a0001 a0006 a0007 |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
missense_variant | MODERATE | c.489G>A | p.Met163Ile | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/14 | 599/5313 | 489/1635 | 163/544 | chr16 | 55528554 | |||
| chr16:55545798 | G | A | 1 | a0005 | 2 | HG02809.hp2 HG02896.hp1 |
missense_variant | MODERATE | c.916G>A | p.Val306Ile | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/14 | 1026/5313 | 916/1635 | 306/544 | chr16 | 55545798 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:55525576 | A | T | 1 | a0001c0011 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.240A>T | p.Ala80Ala | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/14 | 350/5313 | 240/1635 | 80/544 | chr16 | 55525576 | |||
| chr16:55574675 | G | A | 3 | a0001c0003 a0002c0005 a0003c0010 |
36 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(33): Show |
synonymous_variant | LOW | c.1260G>A | p.Leu420Leu | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/14 | 1370/5313 | 1260/1635 | 420/544 | chr16 | 55574675 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:55509138 | G | T | 6 | a0003c0004t0022 a0003c0004t0039 a0003c0004t0074 others(3): Show |
10 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-44G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/14 | 44 | chr16 | 55509138 | ||||||
| chr16:55509141 | C | T | 1 | a0003c0004t0077 | 1 | NA18747.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-41C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/14 | chr16 | 55509141 | |||||||
| chr16:55509161 | G | C | 13 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0007 others(10): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
5_prime_UTR_variant | MODIFIER | c.-21G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/14 | 21 | chr16 | 55509161 | ||||||
| chr16:55583205 | A | T | 1 | a0002c0001t0073 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*107A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 107 | chr16 | 55583205 | ||||||
| chr16:55583215 | C | T | 62 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(59): Show |
179 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*117C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 117 | chr16 | 55583215 | ||||||
| chr16:55583290 | G | T | 63 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(60): Show |
180 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*192G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 192 | chr16 | 55583290 | ||||||
| chr16:55584035 | A | C | 2 | a0002c0001t0018 a0002c0001t0055 |
5 | HG02723.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*937A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 937 | chr16 | 55584035 | ||||||
| chr16:55584296 | G | A | 2 | a0003c0006t0023 a0003c0006t0047 |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1198G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 1198 | chr16 | 55584296 | ||||||
| chr16:55584539 | A | G | 66 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(63): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1441A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 1441 | chr16 | 55584539 | ||||||
| chr16:55584562 | T | A | 1 | a0002c0001t0057 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1464T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 1464 | chr16 | 55584562 | ||||||
| chr16:55584575 | T | C | 1 | a0002c0001t0058 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1477T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 1477 | chr16 | 55584575 | ||||||
| chr16:55584755 | A | G | 12 | a0001c0003t0010 a0001c0003t0011 a0001c0003t0021 others(9): Show |
31 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1657A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 1657 | chr16 | 55584755 | ||||||
| chr16:55584915 | AGAGT | A | 28 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0006 others(25): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1819_*1822delAGTG | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 1819 | INFO_REALIGN_3_PRIME | chr16 | 55584915 | |||||
| chr16:55585552 | T | C | 1 | a0002c0001t0048 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2454T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 2454 | chr16 | 55585552 | ||||||
| chr16:55585587 | T | C | 8 | a0001c0002t0040 a0001c0003t0069 a0001c0003t0070 others(5): Show |
15 | HG01934.hp2 HG02080.hp2 HG02132.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2489T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 2489 | chr16 | 55585587 | ||||||
| chr16:55585662 | C | T | 28 | a0001c0002t0003 a0001c0002t0016 a0001c0002t0025 others(25): Show |
64 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2564C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 2564 | chr16 | 55585662 | ||||||
| chr16:55585747 | C | T | 3 | a0001c0003t0034 a0002c0001t0067 a0002c0005t0063 |
4 | HG02258.hp2 HG02615.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2649C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 2649 | chr16 | 55585747 | ||||||
| chr16:55585894 | T | C | 1 | a0002c0001t0064 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2796T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 2796 | chr16 | 55585894 | ||||||
| chr16:55585992 | T | C | 4 | a0001c0002t0050 a0001c0003t0072 a0002c0001t0033 others(1): Show |
5 | HG01106.hp2 HG02615.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2894T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 2894 | chr16 | 55585992 | ||||||
| chr16:55586023 | G | T | 1 | a0002c0001t0066 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2925G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 2925 | chr16 | 55586023 | ||||||
| chr16:55586063 | T | G | 1 | a0002c0001t0027 | 2 | HG02622.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2965T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 2965 | chr16 | 55586063 | ||||||
| chr16:55586125 | CAAAT | C | 13 | a0001c0002t0008 a0001c0002t0016 a0001c0002t0029 others(10): Show |
28 | HG00558.hp1 HG00597.hp2 HG01257.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3030_*3033delATAA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3030 | INFO_REALIGN_3_PRIME | chr16 | 55586125 | |||||
| chr16:55586295 | G | A | 1 | a0001c0003t0034 | 2 | HG02615.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3197G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3197 | chr16 | 55586295 | ||||||
| chr16:55586325 | A | G | 1 | a0002c0001t0027 | 2 | HG02622.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3227A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3227 | chr16 | 55586325 | ||||||
| chr16:55586336 | C | T | 25 | a0001c0002t0005 a0001c0002t0007 a0001c0002t0017 others(22): Show |
67 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*3238C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3238 | chr16 | 55586336 | ||||||
| chr16:55586347 | A | C | 16 | a0001c0002t0005 a0001c0002t0007 a0001c0002t0017 others(13): Show |
47 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3249A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3249 | chr16 | 55586347 | ||||||
| chr16:55586379 | C | T | 52 | a0001c0002t0004 a0001c0002t0005 a0001c0002t0006 others(49): Show |
149 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*3281C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3281 | chr16 | 55586379 | ||||||
| chr16:55586413 | G | C | 16 | a0001c0002t0005 a0001c0002t0007 a0001c0002t0017 others(13): Show |
47 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3315G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3315 | chr16 | 55586413 | ||||||
| chr16:55586538 | T | C | 2 | a0002c0001t0028 a0002c0001t0051 |
3 | HG02572.hp1 HG03130.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3440T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3440 | chr16 | 55586538 | ||||||
| chr16:55586539 | T | TACATTTT others(55): Show |
26 | a0001c0002t0005 a0001c0002t0007 a0001c0002t0017 others(23): Show |
68 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3449_*3450insAAAA others(58): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3450 | INFO_REALIGN_3_PRIME | chr16 | 55586539 | |||||
| chr16:55586548 | C | A | 1 | a0003c0006t0023 | 3 | HG02647.hp1 HG03195.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3450C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3450 | chr16 | 55586548 | ||||||
| chr16:55586549 | A | AAAT | 1 | a0003c0006t0023 | 3 | HG02647.hp1 HG03195.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3452_*3453insATA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3453 | INFO_REALIGN_3_PRIME | chr16 | 55586549 | |||||
| chr16:55586598 | TG | T | 7 | a0001c0002t0014 a0001c0003t0059 a0002c0001t0014 others(4): Show |
11 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3501delG | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3501 | chr16 | 55586598 | ||||||
| chr16:55586621 | G | A | 2 | a0001c0002t0036 a0002c0001t0027 |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3523G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3523 | chr16 | 55586621 | ||||||
| chr16:55586634 | A | G | 16 | a0001c0002t0005 a0001c0002t0007 a0001c0002t0017 others(13): Show |
47 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3536A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 14/14 | 3536 | chr16 | 55586634 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:55509379 | G | A | 1 | a0002c0001t0012g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.171+27G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509379 | |||||||
| chr16:55509389 | G | A | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.171+37G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509389 | |||||||
| chr16:55509410 | G | T | 67 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(64): Show |
78 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.171+58G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509410 | |||||||
| chr16:55509501 | C | T | 9 | a0001c0002t0001g0261 a0001c0002t0001g0263 a0001c0002t0001g0265 others(6): Show |
9 | HG00642.hp2 HG01069.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.171+149C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509501 | |||||||
| chr16:55509553 | C | T | 1 | a0003c0004t0022g0212 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.171+201C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509553 | |||||||
| chr16:55509569 | C | T | 1 | a0002c0001t0003g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.171+217C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509569 | |||||||
| chr16:55509588 | C | T | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.171+236C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509588 | |||||||
| chr16:55509617 | C | T | 1 | a0001c0003t0072g0210 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.171+265C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509617 | |||||||
| chr16:55509674 | A | T | 2 | a0001c0003t0010g0208 a0001c0003t0011g0209 |
2 | HG02074.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.171+322A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509674 | |||||||
| chr16:55509728 | A | G | 19 | a0001c0002t0002g0008 a0001c0002t0003g0025 a0001c0002t0003g0204 others(16): Show |
23 | HG00140.hp1 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.171+376A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509728 | |||||||
| chr16:55509735 | G | A | 122 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(119): Show |
133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.171+383G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509735 | |||||||
| chr16:55509966 | T | C | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.171+614T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509966 | |||||||
| chr16:55509991 | C | CT | 10 | a0001c0003t0037g0206 a0001c0003t0037g0207 a0002c0001t0002g0192 others(7): Show |
11 | HG00597.hp2 HG02083.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+656dupT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT | 8 | a0001c0002t0001g0213 a0001c0002t0001g0261 a0001c0002t0004g0214 others(5): Show |
8 | HG01069.hp2 HG02004.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.171+650_171+656dup others(7): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(1): Show |
78 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(75): Show |
89 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.171+649_171+656dup others(8): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(2): Show |
18 | a0001c0002t0001g0251 a0001c0002t0001g0252 a0001c0002t0001g0253 others(15): Show |
18 | HG01433.hp1 HG02071.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.171+648_171+656dup others(9): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(4): Show |
1 | a0001c0002t0007g0260 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.171+646_171+656dup others(11): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(7): Show |
7 | a0001c0002t0009g0067 a0001c0002t0009g0068 a0001c0002t0009g0069 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+643_171+656dup others(14): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(8): Show |
3 | a0001c0002t0009g0074 a0001c0002t0031g0073 a0001c0002t0031g0075 |
3 | HG02109.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.171+642_171+656dup others(15): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(9): Show |
3 | a0001c0003t0010g0076 a0001c0003t0010g0077 a0001c0003t0060g0078 |
3 | HG00733.hp1 HG02970.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.171+641_171+656dup others(16): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(10): Show |
1 | a0001c0003t0059g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.171+640_171+656dup others(17): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(12): Show |
1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.171+656_171+657ins others(19): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(17): Show |
1 | a0001c0002t0016g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.171+656_171+657ins others(24): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(18): Show |
1 | a0001c0002t0006g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.171+656_171+657ins others(25): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(22): Show |
1 | a0001c0002t0036g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.171+656_171+657ins others(29): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | C | CTTTTTTT others(31): Show |
1 | a0001c0002t0016g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.171+656_171+657ins others(38): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55509991 | CT | C | 8 | a0001c0002t0006g0194 a0002c0001t0005g0085 a0002c0001t0005g0087 others(5): Show |
8 | HG02155.hp1 HG02155.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+656delT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55509991 | ||||||
| chr16:55510115 | G | C | 1 | a0001c0002t0004g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.171+763G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55510115 | |||||||
| chr16:55510455 | G | T | 4 | a0003c0004t0022g0212 a0003c0004t0039g0186 a0003c0004t0039g0187 others(1): Show |
4 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+1103G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55510455 | |||||||
| chr16:55510637 | G | A | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.171+1285G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55510637 | |||||||
| chr16:55510856 | C | T | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+1504C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55510856 | |||||||
| chr16:55511089 | T | C | 16 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(13): Show |
17 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.171+1737T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511089 | |||||||
| chr16:55511110 | T | C | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+1758T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511110 | |||||||
| chr16:55511290 | T | G | 7 | a0002c0001t0009g0093 a0002c0001t0019g0091 a0002c0001t0024g0090 others(4): Show |
8 | HG02559.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+1938T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511290 | |||||||
| chr16:55511396 | T | C | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+2044T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511396 | |||||||
| chr16:55511434 | A | G | 146 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(143): Show |
160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.171+2082A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511434 | |||||||
| chr16:55511579 | G | A | 4 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0014g0094 others(1): Show |
4 | HG02976.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+2227G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511579 | |||||||
| chr16:55511599 | T | A | 32 | a0001c0002t0002g0033 a0001c0002t0005g0058 a0001c0002t0009g0067 others(29): Show |
32 | HG00609.hp2 HG00733.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.171+2247T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511599 | |||||||
| chr16:55511625 | A | T | 8 | a0001c0003t0010g0063 a0001c0003t0011g0061 a0001c0003t0021g0056 others(5): Show |
8 | HG01168.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+2273A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511625 | |||||||
| chr16:55511646 | T | C | 1 | a0002c0001t0024g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.171+2294T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511646 | |||||||
| chr16:55511695 | G | A | 151 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(148): Show |
165 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.171+2343G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511695 | |||||||
| chr16:55511700 | A | G | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.171+2348A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511700 | |||||||
| chr16:55511715 | G | A | 1 | a0002c0001t0064g0098 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.171+2363G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511715 | |||||||
| chr16:55511818 | T | C | 1 | a0001c0002t0013g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.171+2466T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511818 | |||||||
| chr16:55511901 | G | C | 5 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0045g0022 others(2): Show |
6 | NA18968.hp2 NA18971.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+2549G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511901 | |||||||
| chr16:55511938 | G | A | 1 | a0002c0001t0003g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.171+2586G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511938 | |||||||
| chr16:55511975 | G | A | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+2623G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511975 | |||||||
| chr16:55512252 | G | A | 1 | a0002c0001t0006g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.171+2900G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55512252 | |||||||
| chr16:55512256 | A | G | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.171+2904A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55512256 | |||||||
| chr16:55512344 | C | A | 7 | a0002c0001t0009g0093 a0002c0001t0019g0091 a0002c0001t0024g0090 others(4): Show |
8 | HG02559.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+2992C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55512344 | |||||||
| chr16:55512411 | C | T | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+3059C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55512411 | |||||||
| chr16:55512416 | C | T | 7 | a0002c0001t0009g0093 a0002c0001t0019g0091 a0002c0001t0024g0090 others(4): Show |
8 | HG02559.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+3064C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55512416 | |||||||
| chr16:55512446 | C | T | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.171+3094C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55512446 | |||||||
| chr16:55512540 | C | T | 1 | a0001c0002t0004g0250 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.171+3188C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55512540 | |||||||
| chr16:55512544 | C | CA | 4 | a0001c0002t0016g0045 a0001c0002t0050g0044 a0001c0003t0034g0031 others(1): Show |
4 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+3195dupA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55512544 | ||||||
| chr16:55512643 | G | A | 2 | a0001c0002t0006g0082 a0001c0002t0016g0081 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.171+3291G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55512643 | |||||||
| chr16:55513192 | A | C | 1 | a0001c0002t0004g0259 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.171+3840A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55513192 | |||||||
| chr16:55513229 | G | A | 1 | a0001c0003t0010g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.171+3877G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55513229 | |||||||
| chr16:55513278 | T | A | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+3926T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55513278 | |||||||
| chr16:55513310 | A | G | 1 | a0001c0002t0036g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.171+3958A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55513310 | |||||||
| chr16:55513323 | T | G | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.171+3971T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55513323 | |||||||
| chr16:55513407 | A | G | 1 | a0002c0001t0058g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.171+4055A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55513407 | |||||||
| chr16:55513517 | CA | C | 133 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(130): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.171+4177delA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55513517 | ||||||
| chr16:55513546 | C | T | 1 | a0001c0002t0001g0249 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.171+4194C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55513546 | |||||||
| chr16:55513696 | G | A | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+4344G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55513696 | |||||||
| chr16:55513711 | T | G | 4 | a0003c0004t0022g0212 a0003c0004t0039g0186 a0003c0004t0039g0187 others(1): Show |
4 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+4359T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55513711 | |||||||
| chr16:55513979 | G | A | 1 | a0001c0003t0069g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.171+4627G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55513979 | |||||||
| chr16:55514058 | C | A | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+4706C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55514058 | |||||||
| chr16:55514261 | C | T | 4 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0045g0022 others(1): Show |
5 | NA18968.hp2 NA18971.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+4909C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55514261 | |||||||
| chr16:55514410 | G | C | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.171+5058G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55514410 | |||||||
| chr16:55514453 | A | C | 5 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0013g0029 others(2): Show |
5 | HG02976.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+5101A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55514453 | |||||||
| chr16:55514578 | A | G | 1 | a0001c0003t0011g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.171+5226A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55514578 | |||||||
| chr16:55514709 | A | T | 7 | a0001c0003t0010g0063 a0001c0003t0011g0061 a0001c0003t0021g0056 others(4): Show |
7 | HG01168.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+5357A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55514709 | |||||||
| chr16:55514742 | G | A | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.171+5390G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55514742 | |||||||
| chr16:55514769 | G | T | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.171+5417G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55514769 | |||||||
| chr16:55514818 | T | C | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+5466T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55514818 | |||||||
| chr16:55514890 | T | TTG | 43 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0213 others(40): Show |
50 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.171+5578_171+5579d others(4): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55514890 | ||||||
| chr16:55514890 | T | TTGTG | 35 | a0001c0002t0001g0047 a0001c0002t0001g0049 a0001c0002t0001g0051 others(32): Show |
37 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.171+5576_171+5579d others(6): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55514890 | ||||||
| chr16:55514890 | T | TTGTGTG | 14 | a0001c0002t0001g0027 a0001c0002t0001g0054 a0001c0002t0001g0241 others(11): Show |
17 | HG00423.hp1 HG01081.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.171+5574_171+5579d others(8): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55514890 | ||||||
| chr16:55514890 | T | TTGTGTGT others(1): Show |
10 | a0001c0002t0001g0245 a0001c0002t0001g0248 a0001c0002t0001g0261 others(7): Show |
10 | HG00642.hp2 HG01069.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.171+5572_171+5579d others(10): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55514890 | ||||||
| chr16:55514890 | T | TTGTGTGT others(3): Show |
4 | a0001c0003t0010g0063 a0001c0003t0021g0062 a0001c0003t0021g0064 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+5570_171+5579d others(12): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55514890 | ||||||
| chr16:55514890 | T | TTGTGTGT others(5): Show |
1 | a0001c0002t0029g0055 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.171+5568_171+5579d others(14): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55514890 | ||||||
| chr16:55514890 | TTG | T | 25 | a0001c0002t0001g0220 a0001c0002t0001g0251 a0001c0002t0006g0024 others(22): Show |
28 | HG00609.hp2 HG00621.hp2 HG01515.hp1 others(25): Show |
intron_variant | MODIFIER | c.171+5578_171+5579d others(4): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55514890 | ||||||
| chr16:55514890 | TTGTG | T | 34 | a0001c0002t0002g0033 a0001c0002t0005g0058 a0001c0002t0009g0067 others(31): Show |
35 | HG00408.hp2 HG01069.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.171+5576_171+5579d others(6): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55514890 | ||||||
| chr16:55514890 | TTGTGTG | T | 15 | a0001c0002t0014g0080 a0001c0002t0016g0081 a0002c0001t0012g0101 others(12): Show |
16 | HG01934.hp2 HG02145.hp1 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.171+5574_171+5579d others(8): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55514890 | ||||||
| chr16:55514890 | TTGTGTGT others(1): Show |
T | 5 | a0001c0002t0006g0082 a0001c0002t0016g0084 a0001c0002t0036g0011 others(2): Show |
6 | HG00733.hp1 HG01891.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.171+5572_171+5579d others(10): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55514890 | ||||||
| chr16:55514964 | A | G | 6 | a0002c0001t0018g0018 a0002c0001t0018g0020 a0002c0001t0018g0120 others(3): Show |
7 | HG02258.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+5612A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55514964 | |||||||
| chr16:55515096 | C | T | 1 | a0001c0002t0001g0261 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.171+5744C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515096 | |||||||
| chr16:55515169 | A | G | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+5817A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515169 | |||||||
| chr16:55515247 | T | TAC | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.171+5896_171+5897i others(4): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55515247 | ||||||
| chr16:55515332 | G | A | 6 | a0001c0002t0006g0082 a0001c0002t0014g0080 a0001c0002t0016g0081 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+5980G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515332 | |||||||
| chr16:55515353 | AAAG | A | 6 | a0002c0001t0018g0018 a0002c0001t0018g0020 a0002c0001t0018g0120 others(3): Show |
7 | HG02258.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+6006_171+6008d others(5): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55515353 | ||||||
| chr16:55515480 | T | TAG | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+6128_171+6129i others(4): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515480 | |||||||
| chr16:55515481 | C | T | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+6129C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515481 | |||||||
| chr16:55515483 | G | T | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+6131G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515483 | |||||||
| chr16:55515484 | G | C | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+6132G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515484 | |||||||
| chr16:55515485 | C | A | 87 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(84): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.171+6133C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515485 | |||||||
| chr16:55515700 | G | T | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.171+6348G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515700 | |||||||
| chr16:55515703 | T | C | 4 | a0001c0002t0016g0045 a0001c0002t0050g0044 a0001c0003t0034g0031 others(1): Show |
4 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+6351T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515703 | |||||||
| chr16:55515706 | T | C | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.171+6354T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515706 | |||||||
| chr16:55515761 | G | A | 2 | a0001c0002t0016g0084 a0001c0002t0036g0011 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.171+6409G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515761 | |||||||
| chr16:55515781 | G | A | 2 | a0001c0002t0006g0082 a0001c0002t0016g0081 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.171+6429G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515781 | |||||||
| chr16:55515948 | G | C | 146 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(143): Show |
160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.171+6596G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515948 | |||||||
| chr16:55515999 | A | T | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.171+6647A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55515999 | |||||||
| chr16:55516003 | G | T | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.171+6651G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516003 | |||||||
| chr16:55516130 | G | A | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.171+6778G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516130 | |||||||
| chr16:55516168 | A | G | 1 | a0002c0001t0003g0165 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.171+6816A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516168 | |||||||
| chr16:55516217 | A | G | 14 | a0002c0001t0002g0161 a0002c0001t0002g0164 a0002c0001t0002g0192 others(11): Show |
15 | HG00408.hp2 HG01243.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.171+6865A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516217 | |||||||
| chr16:55516279 | A | AT | 74 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(71): Show |
85 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.171+6933dupT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55516279 | ||||||
| chr16:55516296 | G | T | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.171+6944G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516296 | |||||||
| chr16:55516325 | A | G | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.171+6973A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516325 | |||||||
| chr16:55516383 | G | A | 12 | a0001c0002t0001g0252 a0001c0002t0001g0255 a0001c0002t0001g0261 others(9): Show |
12 | HG00642.hp2 HG01069.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.171+7031G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516383 | |||||||
| chr16:55516434 | A | G | 2 | a0001c0002t0006g0082 a0001c0002t0016g0081 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.171+7082A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516434 | |||||||
| chr16:55516578 | G | A | 79 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(76): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.171+7226G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516578 | |||||||
| chr16:55516794 | A | G | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+7442A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516794 | |||||||
| chr16:55516940 | T | A | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+7588T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55516940 | |||||||
| chr16:55517060 | A | C | 2 | a0001c0002t0013g0040 a0001c0002t0013g0041 |
2 | NA18939.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.171+7708A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55517060 | |||||||
| chr16:55517101 | T | G | 2 | a0001c0002t0001g0268 a0001c0002t0007g0262 |
2 | HG01261.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.171+7749T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55517101 | |||||||
| chr16:55517204 | A | G | 1 | a0002c0001t0012g0105 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.171+7852A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55517204 | |||||||
| chr16:55517400 | C | T | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+8048C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55517400 | |||||||
| chr16:55517445 | C | T | 2 | a0001c0003t0010g0208 a0001c0003t0011g0209 |
2 | HG02074.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.172-8063C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55517445 | |||||||
| chr16:55517678 | C | G | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.172-7830C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55517678 | |||||||
| chr16:55517747 | A | G | 30 | a0001c0002t0002g0033 a0001c0002t0005g0058 a0001c0002t0009g0067 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.172-7761A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55517747 | |||||||
| chr16:55517794 | A | C | 1 | a0004c0007t0003g0184 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.172-7714A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55517794 | |||||||
| chr16:55517850 | A | G | 4 | a0001c0002t0016g0045 a0001c0002t0050g0044 a0001c0003t0034g0031 others(1): Show |
4 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-7658A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55517850 | |||||||
| chr16:55518087 | T | G | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-7421T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518087 | |||||||
| chr16:55518167 | T | A | 1 | a0002c0001t0033g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.172-7341T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518167 | |||||||
| chr16:55518188 | T | A | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.172-7320T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518188 | |||||||
| chr16:55518237 | T | TGAAAACT others(6082): Show |
2 | a0002c0001t0002g0159 a0002c0001t0003g0160 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.172-7254_172-7253i others(6091): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55518237 | ||||||
| chr16:55518253 | TC | T | 5 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0013g0029 others(2): Show |
5 | HG02976.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.172-7254delC | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518253 | |||||||
| chr16:55518275 | A | G | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-7233A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518275 | |||||||
| chr16:55518311 | T | A | 8 | a0001c0003t0010g0063 a0001c0003t0011g0061 a0001c0003t0021g0056 others(5): Show |
8 | HG01168.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-7197T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518311 | |||||||
| chr16:55518442 | A | G | 6 | a0001c0002t0006g0082 a0001c0002t0014g0080 a0001c0002t0016g0081 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.172-7066A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518442 | |||||||
| chr16:55518510 | C | T | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-6998C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518510 | |||||||
| chr16:55518528 | C | T | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.172-6980C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518528 | |||||||
| chr16:55518581 | C | T | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.172-6927C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518581 | |||||||
| chr16:55518785 | G | T | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.172-6723G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518785 | |||||||
| chr16:55518833 | G | A | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-6675G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518833 | |||||||
| chr16:55518882 | G | A | 1 | a0001c0002t0001g0047 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.172-6626G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55518882 | |||||||
| chr16:55519088 | T | TAACCC | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.172-6416_172-6412d others(7): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55519088 | ||||||
| chr16:55519165 | A | G | 1 | a0001c0002t0001g0258 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.172-6343A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519165 | |||||||
| chr16:55519228 | C | T | 1 | a0002c0001t0025g0158 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.172-6280C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519228 | |||||||
| chr16:55519239 | A | G | 151 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(148): Show |
165 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.172-6269A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519239 | |||||||
| chr16:55519246 | G | A | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.172-6262G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519246 | |||||||
| chr16:55519276 | G | A | 11 | a0002c0001t0008g0168 a0003c0004t0022g0022 a0003c0004t0022g0023 others(8): Show |
12 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.172-6232G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519276 | |||||||
| chr16:55519306 | T | C | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.172-6202T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519306 | |||||||
| chr16:55519336 | T | TA | 18 | a0001c0002t0001g0213 a0001c0003t0011g0030 a0001c0003t0011g0043 others(15): Show |
19 | HG01358.hp2 HG02132.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.172-6158dupA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55519336 | ||||||
| chr16:55519336 | TA | T | 14 | a0001c0002t0001g0047 a0001c0002t0001g0220 a0001c0003t0038g0065 others(11): Show |
15 | HG00438.hp2 HG01975.hp2 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-6158delA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55519336 | ||||||
| chr16:55519440 | C | T | 7 | a0002c0001t0009g0093 a0002c0001t0019g0091 a0002c0001t0024g0090 others(4): Show |
8 | HG02559.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-6068C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519440 | |||||||
| chr16:55519508 | C | CA | 121 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(118): Show |
133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.172-5989dupA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55519508 | ||||||
| chr16:55519520 | G | A | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.172-5988G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519520 | |||||||
| chr16:55519548 | A | G | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.172-5960A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519548 | |||||||
| chr16:55519624 | T | G | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.172-5884T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519624 | |||||||
| chr16:55519723 | G | T | 4 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0014g0094 others(1): Show |
4 | HG02976.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-5785G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519723 | |||||||
| chr16:55519771 | G | T | 2 | a0001c0002t0006g0082 a0001c0002t0016g0081 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.172-5737G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519771 | |||||||
| chr16:55520047 | A | T | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-5461A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55520047 | |||||||
| chr16:55520313 | G | A | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-5195G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55520313 | |||||||
| chr16:55520352 | C | T | 1 | a0002c0001t0033g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.172-5156C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55520352 | |||||||
| chr16:55520527 | A | C | 1 | a0002c0001t0003g0165 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.172-4981A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55520527 | |||||||
| chr16:55520573 | A | G | 1 | a0002c0001t0002g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.172-4935A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55520573 | |||||||
| chr16:55520790 | C | T | 75 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(72): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.172-4718C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55520790 | |||||||
| chr16:55520825 | C | T | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-4683C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55520825 | |||||||
| chr16:55520826 | G | A | 5 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0045g0022 others(2): Show |
6 | NA18968.hp2 NA18971.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-4682G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55520826 | |||||||
| chr16:55520946 | A | G | 3 | a0001c0002t0016g0084 a0001c0002t0036g0011 a0007c0009t0014g0083 |
4 | HG02896.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-4562A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55520946 | |||||||
| chr16:55521123 | G | C | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-4385G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55521123 | |||||||
| chr16:55521365 | G | A | 151 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(148): Show |
165 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.172-4143G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55521365 | |||||||
| chr16:55521410 | C | G | 1 | a0002c0001t0008g0086 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.172-4098C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55521410 | |||||||
| chr16:55521922 | C | A | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-3586C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55521922 | |||||||
| chr16:55521947 | C | T | 1 | a0002c0001t0052g0124 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.172-3561C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55521947 | |||||||
| chr16:55521975 | G | A | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-3533G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55521975 | |||||||
| chr16:55521975 | G | T | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-3533G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55521975 | |||||||
| chr16:55521988 | G | A | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.172-3520G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55521988 | |||||||
| chr16:55522023 | CAT | C | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-3482_172-3481d others(4): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55522023 | ||||||
| chr16:55522490 | C | G | 2 | a0002c0001t0008g0096 a0002c0001t0008g0097 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.172-3018C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55522490 | |||||||
| chr16:55522533 | TGAA | T | 11 | a0001c0003t0010g0063 a0001c0003t0011g0061 a0001c0003t0021g0056 others(8): Show |
12 | HG01168.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-2965_172-2963d others(5): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55522533 | ||||||
| chr16:55522549 | A | G | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-2959A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55522549 | |||||||
| chr16:55522627 | T | TA | 4 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0014g0094 others(1): Show |
4 | HG02976.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-2880dupA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 55522627 | ||||||
| chr16:55522769 | T | C | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-2739T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55522769 | |||||||
| chr16:55522814 | G | T | 1 | a0007c0009t0014g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.172-2694G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55522814 | |||||||
| chr16:55523551 | G | A | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-1957G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55523551 | |||||||
| chr16:55523652 | T | C | 2 | a0001c0002t0001g0265 a0001c0002t0001g0269 |
2 | HG00642.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.172-1856T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55523652 | |||||||
| chr16:55523848 | G | T | 6 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(3): Show |
6 | HG00639.hp2 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1660G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55523848 | |||||||
| chr16:55523849 | G | A | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-1659G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55523849 | |||||||
| chr16:55523871 | A | C | 1 | a0002c0001t0006g0111 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.172-1637A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55523871 | |||||||
| chr16:55523881 | T | C | 1 | a0001c0002t0005g0058 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.172-1627T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55523881 | |||||||
| chr16:55523906 | G | T | 125 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(122): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-1602G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55523906 | |||||||
| chr16:55523997 | A | G | 6 | a0002c0001t0018g0018 a0002c0001t0018g0020 a0002c0001t0018g0120 others(3): Show |
7 | HG02258.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.172-1511A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55523997 | |||||||
| chr16:55524075 | G | A | 1 | a0001c0002t0007g0233 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.172-1433G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524075 | |||||||
| chr16:55524076 | C | A | 1 | a0001c0002t0007g0233 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.172-1432C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524076 | |||||||
| chr16:55524157 | C | T | 1 | a0002c0001t0003g0156 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.172-1351C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524157 | |||||||
| chr16:55524296 | G | A | 79 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(76): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.172-1212G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524296 | |||||||
| chr16:55524459 | G | C | 6 | a0001c0002t0004g0009 a0001c0002t0007g0009 a0001c0002t0007g0233 others(3): Show |
7 | HG00408.hp1 HG00621.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-1049G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524459 | |||||||
| chr16:55524647 | C | A | 146 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(143): Show |
160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.172-861C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524647 | |||||||
| chr16:55524653 | A | C | 1 | a0002c0001t0002g0155 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.172-855A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524653 | |||||||
| chr16:55524664 | C | T | 134 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(131): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.172-844C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524664 | |||||||
| chr16:55524773 | A | C | 4 | a0001c0002t0016g0045 a0001c0002t0050g0044 a0001c0003t0034g0031 others(1): Show |
4 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-735A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524773 | |||||||
| chr16:55524818 | G | A | 87 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(84): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.172-690G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524818 | |||||||
| chr16:55524837 | G | A | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.172-671G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524837 | |||||||
| chr16:55524843 | C | T | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-665C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524843 | |||||||
| chr16:55524898 | A | G | 1 | a0002c0001t0064g0098 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.172-610A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524898 | |||||||
| chr16:55524902 | G | T | 2 | a0001c0002t0001g0255 a0001c0002t0004g0222 |
2 | HG01433.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.172-606G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55524902 | |||||||
| chr16:55525105 | C | T | 2 | a0001c0002t0001g0268 a0001c0002t0007g0262 |
2 | HG01261.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.172-403C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55525105 | |||||||
| chr16:55525177 | C | T | 79 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(76): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.172-331C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55525177 | |||||||
| chr16:55525294 | A | G | 10 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0022g0212 others(7): Show |
11 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-214A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55525294 | |||||||
| chr16:55525698 | A | G | 1 | a0001c0002t0003g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.311+51A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55525698 | |||||||
| chr16:55525810 | C | A | 1 | a0002c0001t0006g0100 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.311+163C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55525810 | |||||||
| chr16:55526031 | A | G | 3 | a0001c0002t0016g0045 a0001c0003t0034g0031 a0001c0003t0034g0046 |
3 | HG02615.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.311+384A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55526031 | |||||||
| chr16:55526086 | T | G | 5 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0013g0029 others(2): Show |
5 | HG02976.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+439T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55526086 | |||||||
| chr16:55526146 | A | C | 5 | a0003c0004t0022g0022 a0003c0004t0022g0023 a0003c0004t0045g0022 others(2): Show |
6 | NA18968.hp2 NA18971.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.311+499A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55526146 | |||||||
| chr16:55526169 | G | T | 157 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(154): Show |
172 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.311+522G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55526169 | |||||||
| chr16:55526177 | T | G | 1 | a0001c0002t0050g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.311+530T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55526177 | |||||||
| chr16:55526379 | C | G | 1 | a0002c0001t0024g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.311+732C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55526379 | |||||||
| chr16:55526479 | C | T | 3 | a0001c0002t0016g0084 a0001c0002t0036g0011 a0007c0009t0014g0083 |
4 | HG02896.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.311+832C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55526479 | |||||||
| chr16:55526704 | C | T | 1 | a0002c0001t0005g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.311+1057C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55526704 | |||||||
| chr16:55526838 | A | G | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.311+1191A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55526838 | |||||||
| chr16:55526898 | A | G | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.311+1251A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55526898 | |||||||
| chr16:55527155 | A | G | 127 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(124): Show |
139 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.312-1222A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527155 | |||||||
| chr16:55527168 | T | C | 137 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(134): Show |
150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.312-1209T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527168 | |||||||
| chr16:55527322 | A | G | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.312-1055A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527322 | |||||||
| chr16:55527373 | G | A | 1 | a0002c0001t0012g0028 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.312-1004G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527373 | |||||||
| chr16:55527395 | G | A | 2 | a0002c0001t0048g0166 a0002c0005t0063g0167 |
2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.312-982G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527395 | |||||||
| chr16:55527479 | C | CA | 35 | a0001c0002t0002g0033 a0001c0002t0005g0058 a0001c0002t0009g0067 others(32): Show |
35 | HG00609.hp2 HG00733.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.312-880dupA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 55527479 | ||||||
| chr16:55527479 | CA | C | 25 | a0001c0002t0003g0204 a0001c0003t0010g0063 a0001c0003t0011g0061 others(22): Show |
27 | HG01099.hp1 HG01168.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.312-880delA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 55527479 | ||||||
| chr16:55527583 | C | G | 30 | a0001c0002t0002g0033 a0001c0002t0005g0058 a0001c0002t0009g0067 others(27): Show |
30 | HG00609.hp2 HG00733.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.312-794C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527583 | |||||||
| chr16:55527625 | C | T | 1 | a0001c0002t0008g0203 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.312-752C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527625 | |||||||
| chr16:55527628 | T | C | 2 | a0001c0002t0006g0082 a0001c0002t0016g0081 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.312-749T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527628 | |||||||
| chr16:55527699 | G | T | 1 | a0002c0001t0064g0098 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.312-678G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527699 | |||||||
| chr16:55527753 | A | G | 153 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(150): Show |
167 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.312-624A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527753 | |||||||
| chr16:55527764 | C | G | 1 | a0002c0001t0005g0123 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.312-613C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527764 | |||||||
| chr16:55527901 | T | C | 32 | a0001c0002t0002g0033 a0001c0002t0005g0058 a0001c0002t0009g0067 others(29): Show |
32 | HG00609.hp2 HG00733.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.312-476T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527901 | |||||||
| chr16:55527936 | T | C | 1 | a0002c0001t0003g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.312-441T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527936 | |||||||
| chr16:55527948 | A | T | 1 | a0002c0001t0008g0086 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.312-429A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527948 | |||||||
| chr16:55528255 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.312-122C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55528255 | |||||||
| chr16:55528345 | G | A | 273 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(270): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.312-32G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55528345 | |||||||
| chr16:55528660 | T | C | 29 | a0002c0001t0002g0121 a0002c0001t0002g0122 a0002c0001t0002g0157 others(26): Show |
32 | HG00558.hp1 HG00639.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.529+66T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/13 | chr16 | 55528660 | |||||||
| chr16:55528726 | G | A | 3 | a0001c0002t0016g0084 a0001c0002t0036g0011 a0007c0009t0014g0083 |
4 | HG02896.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+132G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/13 | chr16 | 55528726 | |||||||
| chr16:55528911 | G | A | 2 | a0001c0002t0007g0235 a0001c0002t0040g0234 |
2 | NA18946.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.529+317G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/13 | chr16 | 55528911 | |||||||
| chr16:55528951 | G | A | 6 | a0002c0001t0002g0192 a0002c0001t0006g0015 a0002c0001t0006g0108 others(3): Show |
7 | HG00408.hp2 HG02056.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.529+357G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/13 | chr16 | 55528951 | |||||||
| chr16:55529104 | G | A | 135 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(132): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.529+510G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/13 | chr16 | 55529104 | |||||||
| chr16:55529305 | AT | A | 8 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 others(5): Show |
9 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.530-520delT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 55529305 | ||||||
| chr16:55529403 | G | A | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.530-432G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/13 | chr16 | 55529403 | |||||||
| chr16:55529808 | G | C | 1 | a0001c0003t0021g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.530-27G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/13 | chr16 | 55529808 | |||||||
| chr16:55529820 | T | G | 2 | a0001c0002t0009g0067 a0001c0002t0009g0070 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.530-15T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 3/13 | chr16 | 55529820 | |||||||
| chr16:55530033 | G | A | 1 | a0007c0009t0014g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.642+86G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530033 | |||||||
| chr16:55530098 | C | A | 136 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(133): Show |
149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.642+151C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530098 | |||||||
| chr16:55530221 | C | G | 1 | a0002c0001t0006g0109 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.642+274C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530221 | |||||||
| chr16:55530366 | G | A | 8 | a0001c0003t0010g0063 a0001c0003t0011g0061 a0001c0003t0021g0056 others(5): Show |
8 | HG01168.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+419G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530366 | |||||||
| chr16:55530486 | C | T | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.642+539C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530486 | |||||||
| chr16:55530492 | TG | T | 113 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(110): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.642+555delG | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 55530492 | ||||||
| chr16:55530494 | G | T | 4 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0014g0094 others(1): Show |
4 | HG02976.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+547G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530494 | |||||||
| chr16:55530496 | G | A | 133 | a0001c0002t0001g0221 a0001c0002t0001g0245 a0001c0002t0002g0008 others(130): Show |
145 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.642+549G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530496 | |||||||
| chr16:55530498 | G | C | 4 | a0002c0001t0018g0018 a0002c0001t0018g0020 a0002c0001t0018g0120 others(1): Show |
5 | HG02723.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+551G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530498 | |||||||
| chr16:55530499 | G | GC | 19 | a0001c0002t0003g0205 a0001c0002t0006g0024 a0001c0002t0009g0067 others(16): Show |
21 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.642+552_642+553ins others(1): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530499 | |||||||
| chr16:55530885 | C | T | 133 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(130): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.642+938C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530885 | |||||||
| chr16:55530988 | C | T | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-926C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55530988 | |||||||
| chr16:55531123 | A | G | 7 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(4): Show |
8 | HG04115.hp2 NA18747.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.643-791A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55531123 | |||||||
| chr16:55531327 | C | T | 2 | a0001c0002t0001g0232 a0001c0002t0004g0214 |
2 | HG02735.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.643-587C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55531327 | |||||||
| chr16:55531328 | G | A | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-586G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55531328 | |||||||
| chr16:55531563 | G | A | 1 | a0001c0003t0072g0210 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.643-351G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55531563 | |||||||
| chr16:55531582 | G | T | 33 | a0001c0002t0009g0067 a0001c0002t0009g0068 a0001c0002t0009g0069 others(30): Show |
34 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.643-332G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55531582 | |||||||
| chr16:55531668 | A | G | 1 | a0002c0001t0005g0153 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.643-246A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55531668 | |||||||
| chr16:55531794 | C | A | 49 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(46): Show |
51 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.643-120C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55531794 | |||||||
| chr16:55531795 | CTTTTA | C | 2 | a0001c0002t0016g0084 a0001c0002t0036g0011 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.643-114_643-110del others(5): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 55531795 | ||||||
| chr16:55531835 | T | G | 49 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(46): Show |
51 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.643-79T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55531835 | |||||||
| chr16:55531854 | G | A | 3 | a0002c0001t0002g0016 a0002c0001t0003g0007 a0002c0001t0006g0175 |
6 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.643-60G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55531854 | |||||||
| chr16:55531887 | T | C | 1 | a0001c0002t0009g0068 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.643-27T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 4/13 | chr16 | 55531887 | |||||||
| chr16:55532234 | C | T | 2 | a0002c0001t0019g0140 a0002c0001t0056g0141 |
2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.703+260C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 5/13 | chr16 | 55532234 | |||||||
| chr16:55532357 | T | C | 3 | a0002c0001t0024g0017 a0002c0001t0030g0019 a0002c0001t0033g0143 |
5 | HG01106.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+383T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 5/13 | chr16 | 55532357 | |||||||
| chr16:55532397 | C | T | 56 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(53): Show |
59 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.703+423C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 5/13 | chr16 | 55532397 | |||||||
| chr16:55532561 | A | G | 1 | a0002c0001t0003g0169 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.704-263A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 5/13 | chr16 | 55532561 | |||||||
| chr16:55532562 | G | A | 2 | a0001c0002t0016g0084 a0001c0002t0036g0011 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.704-262G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 5/13 | chr16 | 55532562 | |||||||
| chr16:55532604 | A | G | 6 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(3): Show |
7 | HG04115.hp2 NA18968.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-220A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 5/13 | chr16 | 55532604 | |||||||
| chr16:55532645 | T | TA | 231 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(228): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.704-167dupA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 55532645 | ||||||
| chr16:55532645 | TA | T | 6 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(3): Show |
7 | HG04115.hp2 NA18968.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-167delA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 55532645 | ||||||
| chr16:55533067 | C | T | 7 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(4): Show |
8 | HG04115.hp2 NA18747.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.762+185C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55533067 | |||||||
| chr16:55533110 | T | G | 1 | a0002c0001t0054g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.762+228T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55533110 | |||||||
| chr16:55533168 | G | T | 1 | a0002c0001t0015g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.762+286G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55533168 | |||||||
| chr16:55533406 | G | GGTTTTTT | 5 | a0001c0003t0010g0063 a0001c0003t0011g0030 a0001c0003t0021g0060 others(2): Show |
5 | HG02451.hp1 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+524_762+525ins others(7): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55533406 | |||||||
| chr16:55533406 | G | GT | 17 | a0001c0002t0006g0194 a0002c0001t0002g0117 a0002c0001t0002g0164 others(14): Show |
17 | HG00621.hp2 HG01891.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.762+546dupT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 55533406 | ||||||
| chr16:55533406 | G | GTTTT | 5 | a0002c0001t0019g0142 a0003c0004t0022g0023 a0003c0004t0039g0187 others(2): Show |
6 | HG00438.hp2 HG03491.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.762+543_762+546dup others(4): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 55533406 | ||||||
| chr16:55533406 | G | GTTTTTT | 8 | a0001c0002t0006g0082 a0001c0002t0016g0045 a0001c0002t0016g0081 others(5): Show |
9 | HG01891.hp2 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.762+541_762+546dup others(6): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 55533406 | ||||||
| chr16:55533406 | G | GTTTTTTT | 20 | a0001c0002t0009g0069 a0001c0002t0013g0040 a0001c0002t0013g0066 others(17): Show |
21 | HG00597.hp2 HG00733.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.762+540_762+546dup others(7): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 55533406 | ||||||
| chr16:55533406 | G | GTTTTTTT others(1): Show |
16 | a0001c0002t0009g0067 a0001c0002t0009g0068 a0001c0002t0009g0070 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.762+539_762+546dup others(8): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 55533406 | ||||||
| chr16:55533406 | G | GTTTTTTT others(3): Show |
1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.762+537_762+546dup others(10): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 55533406 | ||||||
| chr16:55533406 | GT | G | 91 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0047 others(88): Show |
104 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.762+546delT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 55533406 | ||||||
| chr16:55533573 | C | T | 1 | a0001c0003t0011g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.762+691C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55533573 | |||||||
| chr16:55533664 | T | C | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.763-779T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55533664 | |||||||
| chr16:55533681 | G | A | 2 | a0001c0002t0016g0084 a0001c0002t0036g0011 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.763-762G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55533681 | |||||||
| chr16:55533800 | T | G | 58 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(55): Show |
60 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.763-643T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55533800 | |||||||
| chr16:55534107 | G | T | 58 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(55): Show |
60 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.763-336G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55534107 | |||||||
| chr16:55534144 | C | T | 1 | a0001c0002t0009g0068 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.763-299C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55534144 | |||||||
| chr16:55534205 | A | G | 58 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(55): Show |
60 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.763-238A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 6/13 | chr16 | 55534205 | |||||||
| chr16:55534733 | G | A | 75 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(72): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.797+256G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55534733 | |||||||
| chr16:55535152 | G | C | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.797+675G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535152 | |||||||
| chr16:55535176 | C | T | 1 | a0002c0001t0009g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.797+699C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535176 | |||||||
| chr16:55535451 | C | T | 6 | a0001c0003t0010g0063 a0001c0003t0011g0061 a0001c0003t0021g0060 others(3): Show |
6 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.797+974C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535451 | |||||||
| chr16:55535505 | A | G | 266 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(263): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.797+1028A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535505 | |||||||
| chr16:55535627 | A | G | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.797+1150A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535627 | |||||||
| chr16:55535642 | T | C | 58 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(55): Show |
60 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.797+1165T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535642 | |||||||
| chr16:55535685 | A | G | 48 | a0001c0002t0009g0067 a0001c0002t0009g0068 a0001c0002t0009g0069 others(45): Show |
49 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.797+1208A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535685 | |||||||
| chr16:55535700 | C | T | 7 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(4): Show |
8 | HG04115.hp2 NA18747.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.797+1223C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535700 | |||||||
| chr16:55535740 | T | C | 9 | a0001c0002t0001g0261 a0001c0002t0001g0263 a0001c0002t0001g0265 others(6): Show |
9 | HG00642.hp2 HG01069.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.797+1263T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535740 | |||||||
| chr16:55535791 | T | C | 1 | a0003c0004t0039g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.797+1314T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535791 | |||||||
| chr16:55535818 | T | C | 1 | a0001c0003t0011g0042 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.797+1341T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55535818 | |||||||
| chr16:55536193 | G | C | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.798-1385G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55536193 | |||||||
| chr16:55536237 | C | T | 4 | a0003c0004t0022g0212 a0003c0004t0039g0186 a0003c0004t0039g0187 others(1): Show |
4 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.798-1341C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55536237 | |||||||
| chr16:55536268 | G | A | 9 | a0001c0003t0010g0063 a0001c0003t0011g0030 a0001c0003t0011g0043 others(6): Show |
9 | HG01168.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.798-1310G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55536268 | |||||||
| chr16:55536313 | G | A | 1 | a0002c0001t0003g0007 | 3 | HG00280.hp1 HG01074.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.798-1265G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55536313 | |||||||
| chr16:55536489 | G | T | 48 | a0001c0002t0009g0067 a0001c0002t0009g0068 a0001c0002t0009g0069 others(45): Show |
49 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.798-1089G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55536489 | |||||||
| chr16:55536552 | A | G | 1 | a0001c0003t0011g0057 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.798-1026A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55536552 | |||||||
| chr16:55536971 | C | T | 1 | a0002c0001t0018g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.798-607C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55536971 | |||||||
| chr16:55536993 | G | C | 1 | a0002c0001t0006g0175 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.798-585G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55536993 | |||||||
| chr16:55537086 | G | A | 58 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(55): Show |
60 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.798-492G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55537086 | |||||||
| chr16:55537247 | C | T | 2 | a0001c0002t0001g0232 a0001c0002t0004g0214 |
2 | HG02735.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.798-331C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55537247 | |||||||
| chr16:55537248 | G | A | 1 | a0001c0002t0013g0037 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.798-330G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55537248 | |||||||
| chr16:55537312 | G | A | 1 | a0001c0002t0006g0194 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.798-266G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55537312 | |||||||
| chr16:55537387 | TC | T | 61 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(58): Show |
62 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.798-187delC | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 55537387 | ||||||
| chr16:55537391 | C | A | 202 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(199): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.798-187C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55537391 | |||||||
| chr16:55537398 | A | G | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.798-180A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55537398 | |||||||
| chr16:55537459 | T | C | 3 | a0001c0002t0001g0220 a0001c0002t0001g0224 a0001c0002t0004g0218 |
3 | HG01934.hp1 HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.798-119T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55537459 | |||||||
| chr16:55537523 | A | G | 5 | a0002c0001t0018g0018 a0002c0001t0018g0020 a0002c0001t0018g0120 others(2): Show |
6 | HG02615.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.798-55A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 7/13 | chr16 | 55537523 | |||||||
| chr16:55537651 | G | A | 65 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(62): Show |
68 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.852+19G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55537651 | |||||||
| chr16:55537876 | T | C | 1 | a0002c0001t0008g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.852+244T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55537876 | |||||||
| chr16:55537905 | T | C | 1 | a0001c0002t0001g0220 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.852+273T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55537905 | |||||||
| chr16:55537913 | A | G | 186 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(183): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.852+281A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55537913 | |||||||
| chr16:55538027 | A | G | 1 | a0004c0007t0002g0183 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.852+395A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538027 | |||||||
| chr16:55538060 | C | T | 1 | a0001c0002t0001g0258 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.852+428C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538060 | |||||||
| chr16:55538066 | A | G | 1 | a0002c0001t0027g0014 | 2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+434A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538066 | |||||||
| chr16:55538132 | G | A | 1 | a0001c0003t0010g0208 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.852+500G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538132 | |||||||
| chr16:55538189 | T | C | 58 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(55): Show |
60 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.852+557T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538189 | |||||||
| chr16:55538213 | G | A | 1 | a0001c0002t0026g0225 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.852+581G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538213 | |||||||
| chr16:55538242 | A | G | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.852+610A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538242 | |||||||
| chr16:55538248 | G | A | 58 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(55): Show |
60 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.852+616G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538248 | |||||||
| chr16:55538256 | G | A | 65 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(62): Show |
68 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.852+624G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538256 | |||||||
| chr16:55538262 | C | A | 2 | a0001c0002t0016g0084 a0001c0002t0036g0011 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.852+630C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538262 | |||||||
| chr16:55538333 | G | C | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.852+701G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538333 | |||||||
| chr16:55538645 | T | G | 1 | a0002c0001t0033g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.852+1013T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538645 | |||||||
| chr16:55538679 | CA | C | 10 | a0001c0002t0001g0255 a0001c0002t0001g0258 a0001c0002t0001g0263 others(7): Show |
10 | HG00597.hp1 HG01175.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.852+1071delA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 55538679 | ||||||
| chr16:55538679 | CAA | C | 181 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(178): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.852+1070_852+1071d others(4): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 55538679 | ||||||
| chr16:55538679 | CAAA | C | 62 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(59): Show |
64 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.852+1069_852+1071d others(5): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 55538679 | ||||||
| chr16:55538679 | CAAAAAAA others(7): Show |
C | 6 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(3): Show |
7 | HG04115.hp2 NA18968.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.852+1058_852+1071d others(16): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 55538679 | ||||||
| chr16:55538697 | A | G | 3 | a0002c0001t0012g0102 a0002c0001t0012g0103 a0002c0001t0012g0106 |
3 | NA18946.hp1 NA18953.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.852+1065A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538697 | |||||||
| chr16:55538698 | A | G | 58 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(55): Show |
60 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.852+1066A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538698 | |||||||
| chr16:55538765 | A | G | 1 | a0001c0003t0021g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.852+1133A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538765 | |||||||
| chr16:55538863 | A | G | 60 | a0001c0002t0006g0082 a0001c0002t0008g0026 a0001c0002t0008g0203 others(57): Show |
63 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.852+1231A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55538863 | |||||||
| chr16:55539247 | CT | C | 196 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(193): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.852+1626delT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 55539247 | ||||||
| chr16:55539263 | C | CT | 62 | a0001c0002t0006g0082 a0001c0002t0009g0067 a0001c0002t0009g0068 others(59): Show |
64 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.852+1643dupT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 55539263 | ||||||
| chr16:55539282 | G | A | 7 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(4): Show |
8 | HG04115.hp2 NA18747.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.852+1650G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55539282 | |||||||
| chr16:55539282 | G | T | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.852+1650G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55539282 | |||||||
| chr16:55539284 | T | A | 1 | a0002c0001t0033g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.852+1652T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55539284 | |||||||
| chr16:55539313 | C | T | 6 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(3): Show |
7 | HG04115.hp2 NA18968.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.852+1681C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55539313 | |||||||
| chr16:55539409 | G | A | 266 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(263): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.852+1777G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55539409 | |||||||
| chr16:55539698 | A | G | 31 | a0001c0002t0009g0067 a0001c0002t0009g0068 a0001c0002t0009g0069 others(28): Show |
32 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.852+2066A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55539698 | |||||||
| chr16:55540165 | A | G | 1 | a0002c0001t0027g0014 | 2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+2533A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55540165 | |||||||
| chr16:55540374 | T | C | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.852+2742T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55540374 | |||||||
| chr16:55540487 | A | G | 4 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0014g0094 others(1): Show |
4 | HG02976.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+2855A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55540487 | |||||||
| chr16:55540535 | C | G | 7 | a0001c0002t0016g0045 a0001c0002t0050g0044 a0001c0003t0034g0031 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+2903C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55540535 | |||||||
| chr16:55540537 | A | G | 9 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0013g0029 others(6): Show |
9 | HG02572.hp2 HG02647.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+2905A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55540537 | |||||||
| chr16:55540595 | CTG | C | 56 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(53): Show |
59 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.852+2966_852+2967d others(4): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 55540595 | ||||||
| chr16:55541015 | A | G | 56 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(53): Show |
59 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.852+3383A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55541015 | |||||||
| chr16:55541143 | C | T | 195 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(192): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.852+3511C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55541143 | |||||||
| chr16:55541309 | G | T | 1 | a0002c0001t0033g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.852+3677G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55541309 | |||||||
| chr16:55541526 | A | G | 22 | a0001c0002t0013g0037 a0001c0002t0013g0040 a0001c0002t0013g0041 others(19): Show |
23 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.852+3894A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55541526 | |||||||
| chr16:55541659 | T | C | 56 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(53): Show |
59 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.852+4027T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55541659 | |||||||
| chr16:55541758 | G | A | 56 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(53): Show |
59 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.853-3977G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55541758 | |||||||
| chr16:55541913 | C | T | 3 | a0002c0001t0012g0102 a0002c0001t0012g0103 a0002c0001t0012g0106 |
3 | NA18946.hp1 NA18953.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.853-3822C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55541913 | |||||||
| chr16:55542141 | C | CT | 26 | a0001c0002t0005g0058 a0001c0002t0005g0202 a0001c0002t0006g0194 others(23): Show |
29 | HG00558.hp1 HG01099.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.853-3591dupT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 55542141 | ||||||
| chr16:55542198 | G | A | 1 | a0002c0001t0033g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.853-3537G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55542198 | |||||||
| chr16:55542199 | C | T | 1 | a0002c0001t0033g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.853-3536C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55542199 | |||||||
| chr16:55542247 | A | T | 2 | a0001c0002t0001g0232 a0001c0002t0004g0214 |
2 | HG02735.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.853-3488A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55542247 | |||||||
| chr16:55542249 | A | C | 67 | a0001c0002t0001g0245 a0001c0002t0005g0058 a0001c0002t0005g0202 others(64): Show |
73 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.853-3486A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55542249 | |||||||
| chr16:55542501 | A | T | 2 | a0002c0001t0002g0164 a0002c0001t0035g0163 |
2 | NA18972.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.853-3234A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55542501 | |||||||
| chr16:55542626 | A | G | 9 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0013g0029 others(6): Show |
9 | HG02572.hp2 HG02647.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-3109A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55542626 | |||||||
| chr16:55542998 | T | C | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-2737T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55542998 | |||||||
| chr16:55543096 | G | A | 1 | a0001c0002t0007g0262 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.853-2639G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55543096 | |||||||
| chr16:55543333 | T | C | 1 | a0001c0002t0001g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.853-2402T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55543333 | |||||||
| chr16:55543911 | T | C | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-1824T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55543911 | |||||||
| chr16:55544237 | G | GA | 194 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(191): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.853-1491dupA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 55544237 | ||||||
| chr16:55544257 | C | A | 56 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(53): Show |
59 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.853-1478C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55544257 | |||||||
| chr16:55544266 | G | A | 1 | a0001c0002t0004g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.853-1469G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55544266 | |||||||
| chr16:55544462 | G | C | 1 | a0002c0001t0024g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.853-1273G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55544462 | |||||||
| chr16:55544508 | C | T | 186 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(183): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.853-1227C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55544508 | |||||||
| chr16:55544533 | A | G | 1 | a0001c0002t0009g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.853-1202A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55544533 | |||||||
| chr16:55544544 | G | A | 49 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(46): Show |
51 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.853-1191G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55544544 | |||||||
| chr16:55544687 | T | C | 13 | a0001c0002t0001g0252 a0001c0002t0001g0255 a0001c0002t0001g0261 others(10): Show |
13 | HG00642.hp2 HG01069.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-1048T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55544687 | |||||||
| chr16:55544773 | C | G | 2 | a0002c0001t0002g0116 a0002c0001t0066g0138 |
2 | NA18982.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.853-962C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55544773 | |||||||
| chr16:55544775 | C | G | 1 | a0002c0001t0009g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.853-960C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55544775 | |||||||
| chr16:55544965 | T | A | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.853-770T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55544965 | |||||||
| chr16:55545050 | C | T | 4 | a0003c0004t0022g0212 a0003c0004t0039g0186 a0003c0004t0039g0187 others(1): Show |
4 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-685C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55545050 | |||||||
| chr16:55545179 | A | G | 1 | a0002c0001t0033g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.853-556A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55545179 | |||||||
| chr16:55545524 | A | C | 56 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(53): Show |
59 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.853-211A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 8/13 | chr16 | 55545524 | |||||||
| chr16:55545904 | G | A | 56 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(53): Show |
59 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.935+87G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55545904 | |||||||
| chr16:55545979 | A | G | 1 | a0001c0002t0001g0231 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.935+162A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55545979 | |||||||
| chr16:55545987 | G | A | 257 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(254): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.935+170G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55545987 | |||||||
| chr16:55546112 | G | A | 1 | a0001c0002t0004g0218 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.935+295G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55546112 | |||||||
| chr16:55546448 | A | G | 7 | a0001c0002t0016g0045 a0001c0002t0050g0044 a0001c0003t0034g0031 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.935+631A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55546448 | |||||||
| chr16:55546611 | G | A | 3 | a0001c0002t0003g0204 a0001c0002t0006g0196 a0001c0002t0025g0198 |
3 | HG01257.hp1 HG01361.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.935+794G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55546611 | |||||||
| chr16:55546705 | A | G | 1 | a0003c0006t0023g0089 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.935+888A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55546705 | |||||||
| chr16:55546784 | C | G | 32 | a0001c0002t0013g0037 a0001c0002t0013g0040 a0001c0002t0013g0041 others(29): Show |
33 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.935+967C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55546784 | |||||||
| chr16:55546793 | CTTTCT | C | 9 | a0001c0002t0009g0067 a0001c0002t0009g0068 a0001c0002t0009g0069 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.935+978_935+982del others(5): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 55546793 | ||||||
| chr16:55546944 | C | G | 2 | a0002c0001t0002g0159 a0002c0001t0003g0160 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.935+1127C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55546944 | |||||||
| chr16:55547005 | G | A | 1 | a0002c0001t0003g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.935+1188G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55547005 | |||||||
| chr16:55547020 | G | A | 1 | a0002c0001t0008g0112 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.935+1203G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55547020 | |||||||
| chr16:55547128 | G | A | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.935+1311G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55547128 | |||||||
| chr16:55547154 | GA | G | 56 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(53): Show |
59 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.935+1349delA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 55547154 | ||||||
| chr16:55547415 | G | A | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.935+1598G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55547415 | |||||||
| chr16:55547591 | A | G | 186 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(183): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.936-1686A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55547591 | |||||||
| chr16:55547767 | T | A | 1 | a0002c0001t0006g0109 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.936-1510T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55547767 | |||||||
| chr16:55547829 | G | A | 1 | a0001c0002t0009g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.936-1448G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55547829 | |||||||
| chr16:55547875 | C | T | 1 | a0001c0002t0001g0255 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.936-1402C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55547875 | |||||||
| chr16:55547965 | G | A | 186 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(183): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.936-1312G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55547965 | |||||||
| chr16:55547987 | C | T | 5 | a0001c0002t0001g0261 a0001c0002t0001g0266 a0001c0002t0001g0267 others(2): Show |
5 | HG01069.hp2 HG01099.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.936-1290C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55547987 | |||||||
| chr16:55548068 | A | G | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.936-1209A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548068 | |||||||
| chr16:55548131 | A | T | 1 | a0002c0001t0012g0103 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.936-1146A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548131 | |||||||
| chr16:55548229 | C | CT | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.936-1039dupT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 55548229 | ||||||
| chr16:55548530 | A | G | 6 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(3): Show |
7 | HG04115.hp2 NA18968.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.936-747A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548530 | |||||||
| chr16:55548544 | A | G | 9 | a0001c0003t0010g0063 a0001c0003t0011g0030 a0001c0003t0011g0043 others(6): Show |
9 | HG01168.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.936-733A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548544 | |||||||
| chr16:55548603 | A | G | 1 | a0002c0001t0016g0193 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.936-674A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548603 | |||||||
| chr16:55548662 | A | G | 2 | a0002c0001t0002g0164 a0002c0001t0035g0163 |
2 | NA18972.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.936-615A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548662 | |||||||
| chr16:55548665 | G | A | 3 | a0002c0001t0003g0126 a0002c0001t0065g0134 a0002c0001t0067g0139 |
3 | HG02280.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.936-612G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548665 | |||||||
| chr16:55548706 | G | T | 2 | a0001c0002t0009g0067 a0001c0002t0009g0070 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.936-571G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548706 | |||||||
| chr16:55548731 | C | T | 4 | a0002c0001t0018g0018 a0002c0001t0018g0020 a0002c0001t0018g0120 others(1): Show |
5 | HG02723.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.936-546C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548731 | |||||||
| chr16:55548809 | C | G | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.936-468C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548809 | |||||||
| chr16:55548810 | G | A | 1 | a0001c0003t0010g0077 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.936-467G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548810 | |||||||
| chr16:55548810 | G | C | 3 | a0001c0002t0003g0204 a0001c0002t0006g0196 a0001c0002t0025g0198 |
3 | HG01257.hp1 HG01361.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.936-467G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55548810 | |||||||
| chr16:55549227 | C | CTTT | 18 | a0001c0002t0006g0082 a0001c0002t0050g0044 a0001c0003t0010g0063 others(15): Show |
18 | HG00438.hp2 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.936-42_936-40dupTT others(1): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 55549227 | ||||||
| chr16:55549227 | CT | C | 23 | a0001c0002t0002g0033 a0001c0002t0006g0194 a0002c0001t0002g0117 others(20): Show |
24 | HG00621.hp2 HG00741.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.936-40delT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 55549227 | ||||||
| chr16:55549236 | T | A | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.936-41T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55549236 | |||||||
| chr16:55549236 | T | TA | 3 | a0001c0002t0001g0003 a0001c0002t0001g0231 a0001c0002t0004g0003 |
6 | HG00140.hp2 HG00280.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.936-41_936-40insA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55549236 | |||||||
| chr16:55549237 | T | A | 199 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(196): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.936-40T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55549237 | |||||||
| chr16:55549237 | T | TAA | 6 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(3): Show |
7 | HG04115.hp2 NA18968.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.936-33_936-32dupAA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 55549237 | ||||||
| chr16:55549237 | T | TTTA | 29 | a0001c0002t0013g0037 a0001c0002t0013g0040 a0001c0002t0013g0041 others(26): Show |
31 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.936-40_936-39insTT others(1): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55549237 | |||||||
| chr16:55549238 | A | T | 1 | a0001c0003t0034g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.936-39A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 9/13 | chr16 | 55549238 | |||||||
| chr16:55549536 | A | T | 256 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(253): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1061+134A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55549536 | |||||||
| chr16:55549638 | G | A | 186 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(183): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1061+236G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55549638 | |||||||
| chr16:55549859 | T | A | 2 | a0001c0002t0009g0067 a0001c0002t0009g0070 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1061+457T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55549859 | |||||||
| chr16:55549872 | G | T | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1061+470G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55549872 | |||||||
| chr16:55550037 | C | G | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1061+635C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55550037 | |||||||
| chr16:55550087 | A | G | 1 | a0002c0001t0033g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1061+685A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55550087 | |||||||
| chr16:55550166 | A | G | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061+764A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55550166 | |||||||
| chr16:55550316 | G | A | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1062-633G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55550316 | |||||||
| chr16:55550435 | T | G | 2 | a0001c0002t0016g0084 a0001c0002t0036g0011 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1062-514T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55550435 | |||||||
| chr16:55550633 | G | A | 2 | a0002c0001t0065g0134 a0002c0001t0067g0139 |
2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1062-316G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55550633 | |||||||
| chr16:55550679 | G | A | 1 | a0002c0001t0003g0156 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1062-270G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55550679 | |||||||
| chr16:55550745 | C | A | 48 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(45): Show |
50 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1062-204C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55550745 | |||||||
| chr16:55550756 | A | C | 38 | a0001c0002t0013g0037 a0001c0002t0013g0040 a0001c0002t0013g0041 others(35): Show |
39 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.1062-193A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55550756 | |||||||
| chr16:55551332 | TATC | T | 186 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(183): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1215+233_1215+235d others(5): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55551332 | ||||||
| chr16:55551404 | A | G | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+302A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55551404 | |||||||
| chr16:55551487 | A | C | 38 | a0001c0002t0013g0037 a0001c0002t0013g0040 a0001c0002t0013g0041 others(35): Show |
39 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.1215+385A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55551487 | |||||||
| chr16:55551507 | C | T | 1 | a0003c0004t0039g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1215+405C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55551507 | |||||||
| chr16:55551683 | G | T | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+581G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55551683 | |||||||
| chr16:55551692 | T | C | 2 | a0001c0002t0016g0084 a0001c0002t0036g0011 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1215+590T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55551692 | |||||||
| chr16:55551705 | C | T | 250 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(247): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1215+603C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55551705 | |||||||
| chr16:55551756 | T | G | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+654T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55551756 | |||||||
| chr16:55551841 | C | T | 1 | a0006c0012t0041g0223 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1215+739C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55551841 | |||||||
| chr16:55552028 | C | A | 4 | a0003c0004t0022g0212 a0003c0004t0039g0186 a0003c0004t0039g0187 others(1): Show |
4 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+926C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55552028 | |||||||
| chr16:55552312 | A | G | 1 | a0001c0002t0004g0259 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1215+1210A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55552312 | |||||||
| chr16:55552379 | G | A | 186 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(183): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1215+1277G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55552379 | |||||||
| chr16:55552608 | C | T | 71 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(68): Show |
82 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1215+1506C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55552608 | |||||||
| chr16:55552730 | A | G | 7 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(4): Show |
8 | HG04115.hp2 NA18747.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+1628A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55552730 | |||||||
| chr16:55552843 | CAGGATGG others(10): Show |
C | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+1745_1215+176 others(21): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55552843 | ||||||
| chr16:55552910 | T | C | 38 | a0001c0002t0013g0037 a0001c0002t0013g0040 a0001c0002t0013g0041 others(35): Show |
39 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.1215+1808T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55552910 | |||||||
| chr16:55553047 | CAGTT | C | 256 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(253): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1215+1946_1215+194 others(8): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553047 | |||||||
| chr16:55553052 | G | C | 256 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(253): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1215+1950G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553052 | |||||||
| chr16:55553056 | A | AT | 256 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(253): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1215+1954_1215+195 others(5): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553056 | |||||||
| chr16:55553092 | G | A | 9 | a0001c0002t0009g0067 a0001c0002t0009g0068 a0001c0002t0009g0069 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215+1990G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553092 | |||||||
| chr16:55553108 | C | T | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1215+2006C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553108 | |||||||
| chr16:55553115 | G | C | 1 | a0001c0002t0040g0234 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1215+2013G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553115 | |||||||
| chr16:55553187 | G | A | 202 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(199): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1215+2085G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553187 | |||||||
| chr16:55553206 | C | A | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1215+2104C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553206 | |||||||
| chr16:55553237 | CA | C | 54 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(51): Show |
57 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1215+2147delA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55553237 | ||||||
| chr16:55553278 | G | A | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+2176G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553278 | |||||||
| chr16:55553290 | T | C | 256 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(253): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1215+2188T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553290 | |||||||
| chr16:55553461 | G | A | 256 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(253): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1215+2359G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553461 | |||||||
| chr16:55553504 | A | T | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+2402A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553504 | |||||||
| chr16:55553536 | T | A | 1 | a0001c0002t0001g0236 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1215+2434T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553536 | |||||||
| chr16:55553722 | G | A | 1 | a0001c0002t0029g0072 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1215+2620G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553722 | |||||||
| chr16:55553993 | T | A | 6 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(3): Show |
7 | HG04115.hp2 NA18968.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.1215+2891T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553993 | |||||||
| chr16:55554658 | T | G | 1 | a0003c0004t0039g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1215+3556T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55554658 | |||||||
| chr16:55554813 | G | A | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+3711G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55554813 | |||||||
| chr16:55554823 | A | G | 1 | a0001c0003t0021g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1215+3721A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55554823 | |||||||
| chr16:55554835 | C | T | 2 | a0001c0002t0001g0263 a0001c0011t0001g0264 |
2 | HG01175.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1215+3733C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55554835 | |||||||
| chr16:55554836 | G | A | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+3734G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55554836 | |||||||
| chr16:55555294 | G | A | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+4192G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55555294 | |||||||
| chr16:55555377 | A | G | 2 | a0001c0003t0011g0042 a0001c0003t0038g0032 |
2 | HG00609.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1215+4275A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55555377 | |||||||
| chr16:55555463 | C | G | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+4361C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55555463 | |||||||
| chr16:55555553 | G | A | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+4451G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55555553 | |||||||
| chr16:55555589 | C | T | 1 | a0001c0003t0010g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1215+4487C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55555589 | |||||||
| chr16:55555963 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1215+4861C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55555963 | |||||||
| chr16:55556099 | G | A | 22 | a0001c0002t0013g0037 a0001c0002t0013g0040 a0001c0002t0013g0041 others(19): Show |
23 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1215+4997G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556099 | |||||||
| chr16:55556230 | C | T | 186 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(183): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1215+5128C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556230 | |||||||
| chr16:55556259 | G | A | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+5157G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556259 | |||||||
| chr16:55556340 | T | C | 4 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0014g0094 others(1): Show |
4 | HG02976.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+5238T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556340 | |||||||
| chr16:55556380 | A | G | 1 | a0001c0003t0011g0057 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1215+5278A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556380 | |||||||
| chr16:55556433 | T | G | 1 | a0002c0001t0028g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1215+5331T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556433 | |||||||
| chr16:55556458 | T | C | 7 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(4): Show |
8 | HG04115.hp2 NA18747.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+5356T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556458 | |||||||
| chr16:55556546 | G | A | 1 | a0002c0001t0033g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1215+5444G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556546 | |||||||
| chr16:55556561 | A | T | 2 | a0001c0002t0006g0082 a0001c0002t0016g0081 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1215+5459A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556561 | |||||||
| chr16:55556621 | C | T | 22 | a0001c0002t0013g0037 a0001c0002t0013g0040 a0001c0002t0013g0041 others(19): Show |
23 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1215+5519C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556621 | |||||||
| chr16:55556626 | A | T | 1 | a0001c0002t0007g0239 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1215+5524A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556626 | |||||||
| chr16:55556640 | G | T | 1 | a0001c0003t0071g0038 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1215+5538G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556640 | |||||||
| chr16:55556698 | C | A | 56 | a0001c0002t0004g0052 a0001c0002t0006g0082 a0001c0002t0013g0037 others(53): Show |
59 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1215+5596C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556698 | |||||||
| chr16:55556705 | G | A | 23 | a0001c0002t0013g0037 a0001c0002t0013g0040 a0001c0002t0013g0041 others(20): Show |
24 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1215+5603G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556705 | |||||||
| chr16:55556853 | G | A | 2 | a0002c0001t0003g0113 a0002c0001t0003g0211 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1215+5751G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556853 | |||||||
| chr16:55556867 | A | G | 1 | a0001c0002t0003g0025 | 2 | HG00423.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1215+5765A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556867 | |||||||
| chr16:55556879 | C | G | 4 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0014g0094 others(1): Show |
4 | HG02976.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+5777C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556879 | |||||||
| chr16:55556926 | A | G | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+5824A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556926 | |||||||
| chr16:55556995 | T | G | 2 | a0002c0001t0002g0135 a0002c0001t0003g0165 |
2 | NA18942.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1215+5893T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55556995 | |||||||
| chr16:55557661 | T | A | 2 | a0001c0002t0016g0084 a0001c0002t0036g0011 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1215+6559T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55557661 | |||||||
| chr16:55557808 | T | A | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1215+6706T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55557808 | |||||||
| chr16:55557920 | G | A | 186 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(183): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1215+6818G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55557920 | |||||||
| chr16:55558002 | C | T | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+6900C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558002 | |||||||
| chr16:55558021 | A | G | 1 | a0001c0003t0010g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1215+6919A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558021 | |||||||
| chr16:55558245 | T | G | 1 | a0002c0001t0006g0175 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1215+7143T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558245 | |||||||
| chr16:55558249 | C | A | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+7147C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558249 | |||||||
| chr16:55558327 | G | T | 1 | a0002c0001t0048g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1215+7225G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558327 | |||||||
| chr16:55558403 | G | T | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+7301G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558403 | |||||||
| chr16:55558424 | A | T | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+7322A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558424 | |||||||
| chr16:55558546 | C | T | 3 | a0001c0002t0009g0074 a0001c0002t0031g0073 a0001c0002t0031g0075 |
3 | HG02109.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1215+7444C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558546 | |||||||
| chr16:55558661 | A | C | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+7559A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558661 | |||||||
| chr16:55558820 | G | A | 1 | a0001c0002t0031g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1215+7718G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558820 | |||||||
| chr16:55558821 | C | A | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1215+7719C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558821 | |||||||
| chr16:55558905 | A | G | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+7803A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558905 | |||||||
| chr16:55558918 | C | T | 4 | a0002c0001t0012g0102 a0002c0001t0012g0103 a0002c0001t0012g0105 others(1): Show |
4 | NA18946.hp1 NA18953.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+7816C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55558918 | |||||||
| chr16:55559022 | C | T | 2 | a0001c0002t0001g0265 a0001c0002t0001g0269 |
2 | HG00642.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1215+7920C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559022 | |||||||
| chr16:55559326 | T | C | 1 | a0001c0003t0021g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1215+8224T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559326 | |||||||
| chr16:55559385 | T | C | 1 | a0003c0006t0023g0089 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1215+8283T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559385 | |||||||
| chr16:55559478 | C | A | 4 | a0003c0004t0022g0212 a0003c0004t0039g0186 a0003c0004t0039g0187 others(1): Show |
4 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+8376C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559478 | |||||||
| chr16:55559507 | G | T | 1 | a0001c0003t0011g0059 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1215+8405G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559507 | |||||||
| chr16:55559508 | C | T | 1 | a0002c0001t0024g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1215+8406C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559508 | |||||||
| chr16:55559537 | T | C | 3 | a0002c0001t0005g0085 a0002c0001t0005g0150 a0002c0001t0005g0153 |
3 | HG02155.hp1 NA18964.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1215+8435T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559537 | |||||||
| chr16:55559564 | T | C | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+8462T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559564 | |||||||
| chr16:55559768 | G | GA | 70 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(67): Show |
72 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.1215+8682dupA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55559768 | ||||||
| chr16:55559768 | GA | G | 8 | a0001c0002t0001g0249 a0001c0002t0007g0235 a0001c0002t0009g0070 others(5): Show |
8 | HG01069.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+8682delA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55559768 | ||||||
| chr16:55559769 | A | G | 1 | a0002c0001t0027g0014 | 2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1215+8667A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559769 | |||||||
| chr16:55559792 | A | G | 1 | a0001c0003t0038g0032 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1215+8690A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559792 | |||||||
| chr16:55559980 | A | G | 2 | a0002c0005t0010g0021 a0002c0005t0010g0174 |
3 | HG02257.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1215+8878A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55559980 | |||||||
| chr16:55560068 | T | C | 1 | a0002c0001t0027g0014 | 2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1215+8966T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55560068 | |||||||
| chr16:55560564 | T | C | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+9462T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55560564 | |||||||
| chr16:55560854 | T | C | 27 | a0001c0002t0005g0058 a0001c0002t0005g0202 a0002c0001t0005g0001 others(24): Show |
30 | HG00558.hp1 HG01099.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1215+9752T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55560854 | |||||||
| chr16:55560863 | A | G | 186 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(183): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1215+9761A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55560863 | |||||||
| chr16:55560899 | T | C | 109 | a0001c0002t0001g0241 a0001c0002t0001g0245 a0001c0002t0002g0008 others(106): Show |
120 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1215+9797T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55560899 | |||||||
| chr16:55561073 | A | G | 9 | a0002c0001t0008g0096 a0002c0001t0008g0097 a0002c0001t0013g0029 others(6): Show |
9 | HG02572.hp2 HG02647.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215+9971A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55561073 | |||||||
| chr16:55561370 | C | CT | 58 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(55): Show |
62 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1215+10283dupT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55561370 | ||||||
| chr16:55561370 | C | CTT | 189 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(186): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1215+10282_1215+10 others(8): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55561370 | ||||||
| chr16:55561370 | C | CTTT | 8 | a0001c0002t0001g0261 a0001c0002t0001g0267 a0001c0002t0004g0250 others(5): Show |
8 | HG00741.hp1 HG01069.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+10281_1215+10 others(9): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55561370 | ||||||
| chr16:55561574 | A | T | 2 | a0001c0003t0059g0079 a0001c0003t0060g0078 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1215+10472A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55561574 | |||||||
| chr16:55561588 | TA | T | 195 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(192): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1215+10489delA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55561588 | ||||||
| chr16:55561647 | C | T | 6 | a0001c0002t0050g0044 a0001c0003t0034g0031 a0001c0003t0034g0046 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+10545C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55561647 | |||||||
| chr16:55561939 | T | G | 2 | a0002c0001t0015g0170 a0002c0001t0019g0140 |
2 | HG02165.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1215+10837T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55561939 | |||||||
| chr16:55562103 | A | T | 1 | a0004c0007t0002g0183 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1215+11001A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55562103 | |||||||
| chr16:55562160 | C | T | 1 | a0002c0001t0008g0112 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1215+11058C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55562160 | |||||||
| chr16:55562212 | A | G | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+11110A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55562212 | |||||||
| chr16:55562279 | C | T | 1 | a0002c0001t0012g0106 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1215+11177C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55562279 | |||||||
| chr16:55562332 | T | A | 1 | a0002c0001t0012g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1215+11230T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55562332 | |||||||
| chr16:55562377 | T | C | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1215+11275T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55562377 | |||||||
| chr16:55562551 | AAATAT | A | 9 | a0001c0002t0006g0082 a0001c0002t0014g0080 a0001c0002t0016g0081 others(6): Show |
10 | HG00438.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1215+11454_1215+11 others(11): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55562551 | ||||||
| chr16:55562584 | T | A | 1 | a0001c0003t0038g0032 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1215+11482T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55562584 | |||||||
| chr16:55562632 | T | C | 2 | a0001c0002t0016g0084 a0001c0002t0036g0011 |
3 | HG02896.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1215+11530T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55562632 | |||||||
| chr16:55562905 | T | G | 5 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0053 others(2): Show |
5 | HG00639.hp2 HG01081.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216-11726T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55562905 | |||||||
| chr16:55562959 | T | C | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1216-11672T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55562959 | |||||||
| chr16:55563042 | G | T | 55 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(52): Show |
58 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1216-11589G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55563042 | |||||||
| chr16:55563097 | C | T | 1 | a0001c0002t0014g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1216-11534C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55563097 | |||||||
| chr16:55563133 | T | C | 1 | a0002c0001t0002g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1216-11498T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55563133 | |||||||
| chr16:55563306 | T | A | 256 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(253): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1216-11325T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55563306 | |||||||
| chr16:55563489 | A | G | 47 | a0001c0002t0006g0082 a0001c0002t0013g0037 a0001c0002t0013g0040 others(44): Show |
49 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1216-11142A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55563489 | |||||||
| chr16:55563490 | C | T | 58 | a0001c0002t0003g0204 a0001c0002t0006g0082 a0001c0002t0006g0196 others(55): Show |
61 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1216-11141C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55563490 | |||||||
| chr16:55563610 | G | C | 9 | a0001c0003t0010g0063 a0001c0003t0011g0030 a0001c0003t0011g0043 others(6): Show |
9 | HG01168.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1216-11021G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55563610 | |||||||
| chr16:55563806 | A | T | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1216-10825A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55563806 | |||||||
| chr16:55563935 | T | C | 7 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(4): Show |
8 | HG04115.hp2 NA18747.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.1216-10696T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55563935 | |||||||
| chr16:55563973 | C | A | 1 | a0002c0001t0002g0121 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1216-10658C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55563973 | |||||||
| chr16:55564117 | A | C | 7 | a0002c0001t0019g0142 a0003c0004t0022g0022 a0003c0004t0022g0023 others(4): Show |
8 | HG04115.hp2 NA18747.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.1216-10514A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55564117 | |||||||
| chr16:55564408 | G | A | 248 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(245): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1216-10223G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55564408 | |||||||
| chr16:55564525 | T | A | 1 | a0002c0001t0015g0128 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1216-10106T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55564525 | |||||||
| chr16:55564649 | A | G | 2 | a0001c0002t0004g0214 a0001c0002t0013g0066 |
2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1216-9982A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55564649 | |||||||
| chr16:55564770 | A | G | 4 | a0002c0001t0002g0016 a0002c0001t0003g0007 a0002c0001t0003g0169 others(1): Show |
7 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1216-9861A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55564770 | |||||||
| chr16:55564823 | A | G | 9 | a0001c0003t0010g0063 a0001c0003t0011g0030 a0001c0003t0011g0043 others(6): Show |
9 | HG01168.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1216-9808A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55564823 | |||||||
| chr16:55565061 | ATCT | A | 5 | a0002c0001t0057g0129 a0003c0004t0022g0212 a0003c0004t0039g0186 others(2): Show |
5 | HG00438.hp2 HG02698.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-9565_1216-956 others(7): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55565061 | ||||||
| chr16:55565205 | TAAC | T | 80 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(77): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1216-9423_1216-942 others(7): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55565205 | ||||||
| chr16:55565285 | G | A | 2 | a0001c0003t0010g0034 a0001c0003t0071g0038 |
2 | NA18942.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1216-9346G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55565285 | |||||||
| chr16:55565292 | G | A | 1 | a0003c0004t0039g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1216-9339G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55565292 | |||||||
| chr16:55565511 | T | G | 11 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0003c0004t0022g0022 others(8): Show |
12 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.1216-9120T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55565511 | |||||||
| chr16:55565518 | C | T | 1 | a0002c0001t0003g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1216-9113C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55565518 | |||||||
| chr16:55565614 | A | G | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1216-9017A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55565614 | |||||||
| chr16:55565658 | A | C | 170 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(167): Show |
185 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1216-8973A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55565658 | |||||||
| chr16:55565672 | T | C | 1 | a0001c0002t0001g0253 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1216-8959T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55565672 | |||||||
| chr16:55565694 | G | C | 1 | a0001c0002t0005g0202 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1216-8937G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55565694 | |||||||
| chr16:55565762 | C | A | 27 | a0001c0002t0005g0058 a0001c0002t0005g0202 a0002c0001t0005g0001 others(24): Show |
30 | HG00558.hp1 HG01099.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1216-8869C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55565762 | |||||||
| chr16:55566112 | G | A | 35 | a0001c0003t0010g0034 a0001c0003t0010g0036 a0001c0003t0010g0063 others(32): Show |
36 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1216-8519G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55566112 | |||||||
| chr16:55566122 | T | C | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1216-8509T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55566122 | |||||||
| chr16:55566153 | A | G | 2 | a0002c0001t0014g0094 a0002c0001t0014g0095 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1216-8478A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55566153 | |||||||
| chr16:55566216 | T | A | 1 | a0002c0001t0005g0130 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1216-8415T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55566216 | |||||||
| chr16:55566234 | A | G | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-8397A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55566234 | |||||||
| chr16:55566350 | T | G | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1216-8281T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55566350 | |||||||
| chr16:55566382 | T | C | 260 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(257): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1216-8249T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55566382 | |||||||
| chr16:55566483 | T | G | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1216-8148T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55566483 | |||||||
| chr16:55566631 | G | A | 1 | a0003c0006t0023g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1216-8000G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55566631 | |||||||
| chr16:55567051 | G | C | 4 | a0003c0006t0023g0012 a0003c0006t0023g0088 a0003c0006t0023g0089 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-7580G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55567051 | |||||||
| chr16:55567130 | G | A | 1 | a0001c0002t0001g0266 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1216-7501G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55567130 | |||||||
| chr16:55567476 | A | G | 85 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(82): Show |
93 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1216-7155A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55567476 | |||||||
| chr16:55567911 | A | T | 1 | a0002c0001t0066g0138 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1216-6720A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55567911 | |||||||
| chr16:55568134 | TTC | T | 6 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0003c0004t0022g0022 others(3): Show |
7 | HG04115.hp2 NA18960.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1216-6495_1216-649 others(6): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55568134 | ||||||
| chr16:55568148 | T | TA | 165 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(162): Show |
179 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.1216-6475dupA | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55568148 | ||||||
| chr16:55568148 | T | TAA | 4 | a0002c0001t0018g0018 a0002c0001t0018g0020 a0002c0001t0018g0120 others(1): Show |
5 | HG02723.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216-6476_1216-647 others(6): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55568148 | ||||||
| chr16:55568160 | C | CA | 260 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(257): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1216-6471_1216-647 others(5): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55568160 | |||||||
| chr16:55568224 | C | T | 3 | a0002c0001t0003g0172 a0002c0001t0016g0171 a0002c0001t0058g0185 |
3 | HG02258.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1216-6407C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55568224 | |||||||
| chr16:55568332 | C | T | 2 | a0002c0001t0016g0171 a0002c0001t0058g0185 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1216-6299C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55568332 | |||||||
| chr16:55568388 | C | T | 1 | a0003c0004t0039g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1216-6243C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55568388 | |||||||
| chr16:55568483 | C | T | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1216-6148C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55568483 | |||||||
| chr16:55568485 | T | C | 11 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0003c0004t0022g0022 others(8): Show |
12 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.1216-6146T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55568485 | |||||||
| chr16:55568885 | C | T | 1 | a0001c0002t0008g0203 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1216-5746C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55568885 | |||||||
| chr16:55568948 | T | C | 261 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(258): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1216-5683T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55568948 | |||||||
| chr16:55569041 | A | G | 2 | a0002c0001t0014g0094 a0002c0001t0014g0095 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1216-5590A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569041 | |||||||
| chr16:55569077 | G | A | 1 | a0001c0002t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1216-5554G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569077 | |||||||
| chr16:55569249 | C | G | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1216-5382C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569249 | |||||||
| chr16:55569276 | A | G | 166 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(163): Show |
181 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1216-5355A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569276 | |||||||
| chr16:55569288 | C | G | 4 | a0002c0001t0018g0018 a0002c0001t0018g0020 a0002c0001t0018g0120 others(1): Show |
5 | HG02723.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216-5343C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569288 | |||||||
| chr16:55569314 | C | T | 155 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(152): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1216-5317C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569314 | |||||||
| chr16:55569394 | A | G | 1 | a0007c0009t0014g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1216-5237A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569394 | |||||||
| chr16:55569556 | C | T | 91 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(88): Show |
102 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1216-5075C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569556 | |||||||
| chr16:55569587 | A | G | 7 | a0002c0001t0013g0029 a0002c0001t0014g0094 a0002c0001t0014g0095 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1216-5044A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569587 | |||||||
| chr16:55569722 | C | G | 4 | a0002c0001t0018g0018 a0002c0001t0018g0020 a0002c0001t0018g0120 others(1): Show |
5 | HG02723.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216-4909C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569722 | |||||||
| chr16:55569802 | A | T | 1 | a0001c0002t0002g0033 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1216-4829A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55569802 | |||||||
| chr16:55570109 | C | T | 1 | a0002c0001t0016g0171 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1216-4522C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570109 | |||||||
| chr16:55570126 | A | C | 1 | a0001c0002t0006g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1216-4505A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570126 | |||||||
| chr16:55570216 | A | T | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1216-4415A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570216 | |||||||
| chr16:55570541 | G | A | 85 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(82): Show |
93 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1216-4090G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570541 | |||||||
| chr16:55570558 | C | T | 1 | a0001c0002t0001g0230 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1216-4073C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570558 | |||||||
| chr16:55570559 | G | A | 166 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(163): Show |
181 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1216-4072G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570559 | |||||||
| chr16:55570563 | G | C | 1 | a0002c0001t0056g0141 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1216-4068G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570563 | |||||||
| chr16:55570579 | C | T | 6 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0003c0004t0022g0022 others(3): Show |
7 | HG04115.hp2 NA18960.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1216-4052C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570579 | |||||||
| chr16:55570740 | C | T | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1216-3891C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570740 | |||||||
| chr16:55570876 | G | T | 1 | a0002c0001t0008g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1216-3755G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570876 | |||||||
| chr16:55570920 | G | A | 1 | a0002c0001t0058g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1216-3711G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570920 | |||||||
| chr16:55570930 | C | T | 1 | a0002c0001t0009g0115 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1216-3701C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55570930 | |||||||
| chr16:55571110 | A | G | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1216-3521A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55571110 | |||||||
| chr16:55571277 | A | G | 1 | a0001c0002t0035g0197 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1216-3354A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55571277 | |||||||
| chr16:55571329 | T | A | 2 | a0001c0002t0007g0235 a0001c0002t0040g0234 |
2 | NA18946.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1216-3302T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55571329 | |||||||
| chr16:55571409 | C | A | 2 | a0002c0001t0033g0092 a0002c0001t0033g0143 |
2 | HG01106.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1216-3222C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55571409 | |||||||
| chr16:55571564 | C | T | 91 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(88): Show |
101 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1216-3067C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55571564 | |||||||
| chr16:55571581 | G | C | 26 | a0001c0002t0005g0058 a0001c0002t0005g0202 a0002c0001t0005g0001 others(23): Show |
29 | HG00558.hp1 HG01099.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.1216-3050G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55571581 | |||||||
| chr16:55571679 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1216-2952G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55571679 | |||||||
| chr16:55571718 | A | G | 2 | a0002c0005t0010g0021 a0002c0005t0010g0174 |
3 | HG02257.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1216-2913A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55571718 | |||||||
| chr16:55572285 | T | C | 11 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0003c0004t0022g0022 others(8): Show |
12 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.1216-2346T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55572285 | |||||||
| chr16:55572448 | A | G | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1216-2183A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55572448 | |||||||
| chr16:55572624 | A | ATTGACT | 263 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(260): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1216-2004_1216-200 others(10): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55572624 | ||||||
| chr16:55572798 | A | C | 1 | a0001c0002t0005g0202 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1216-1833A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55572798 | |||||||
| chr16:55572818 | G | A | 1 | a0001c0002t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1216-1813G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55572818 | |||||||
| chr16:55572886 | A | T | 1 | a0002c0001t0008g0097 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1216-1745A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55572886 | |||||||
| chr16:55572957 | A | C | 3 | a0001c0002t0009g0074 a0001c0002t0031g0073 a0001c0002t0031g0075 |
3 | HG02109.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1216-1674A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55572957 | |||||||
| chr16:55572957 | A | G | 1 | a0002c0001t0058g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1216-1674A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55572957 | |||||||
| chr16:55573209 | C | T | 1 | a0001c0002t0006g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1216-1422C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573209 | |||||||
| chr16:55573283 | C | A | 4 | a0003c0004t0022g0212 a0003c0004t0039g0186 a0003c0004t0039g0187 others(1): Show |
4 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-1348C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573283 | |||||||
| chr16:55573345 | C | G | 2 | a0001c0002t0001g0265 a0001c0002t0001g0269 |
2 | HG00642.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1216-1286C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573345 | |||||||
| chr16:55573362 | G | A | 29 | a0001c0002t0005g0058 a0001c0002t0005g0202 a0002c0001t0005g0001 others(26): Show |
32 | HG00558.hp1 HG01099.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1216-1269G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573362 | |||||||
| chr16:55573394 | G | GT | 89 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(86): Show |
100 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1216-1226dupT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55573394 | ||||||
| chr16:55573394 | G | T | 1 | a0002c0001t0005g0132 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1216-1237G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573394 | |||||||
| chr16:55573395 | T | G | 1 | a0001c0002t0009g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1216-1236T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573395 | |||||||
| chr16:55573551 | G | A | 1 | a0001c0002t0016g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1216-1080G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573551 | |||||||
| chr16:55573651 | C | T | 5 | a0002c0001t0012g0101 a0002c0001t0012g0102 a0002c0001t0012g0103 others(2): Show |
5 | HG01934.hp2 NA18946.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216-980C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573651 | |||||||
| chr16:55573658 | TTATAATC others(10): Show |
T | 1 | a0002c0001t0002g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1216-971_1216-955d others(19): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55573658 | ||||||
| chr16:55573712 | C | T | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1216-919C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573712 | |||||||
| chr16:55573794 | GTC | G | 6 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0003c0004t0022g0022 others(3): Show |
7 | HG04115.hp2 NA18960.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1216-835_1216-834d others(4): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 55573794 | ||||||
| chr16:55573828 | C | G | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-803C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573828 | |||||||
| chr16:55573833 | T | A | 1 | a0002c0001t0003g0126 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1216-798T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573833 | |||||||
| chr16:55573897 | A | T | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1216-734A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573897 | |||||||
| chr16:55573936 | T | C | 1 | a0002c0001t0008g0112 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1216-695T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573936 | |||||||
| chr16:55573939 | G | A | 1 | a0002c0001t0048g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1216-692G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573939 | |||||||
| chr16:55573964 | A | G | 260 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(257): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1216-667A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55573964 | |||||||
| chr16:55574075 | C | A | 2 | a0002c0001t0008g0096 a0002c0001t0008g0097 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1216-556C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55574075 | |||||||
| chr16:55574120 | G | C | 166 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(163): Show |
181 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1216-511G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55574120 | |||||||
| chr16:55574147 | A | C | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1216-484A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55574147 | |||||||
| chr16:55574334 | A | G | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-297A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55574334 | |||||||
| chr16:55574507 | A | G | 2 | a0001c0002t0006g0082 a0001c0002t0016g0081 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1216-124A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55574507 | |||||||
| chr16:55574598 | C | T | 1 | a0001c0002t0007g0256 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1216-33C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55574598 | |||||||
| chr16:55574936 | C | G | 11 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0003c0004t0022g0022 others(8): Show |
12 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.1314+207C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55574936 | |||||||
| chr16:55574985 | T | TAAAAAAT others(325): Show |
1 | a0002c0001t0033g0143 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1314+271_1314+272i others(334): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 55574985 | ||||||
| chr16:55575030 | G | A | 1 | a0001c0002t0001g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1314+301G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575030 | |||||||
| chr16:55575180 | G | A | 1 | a0002c0001t0035g0163 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1314+451G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575180 | |||||||
| chr16:55575202 | C | T | 11 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0003c0004t0022g0022 others(8): Show |
12 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.1314+473C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575202 | |||||||
| chr16:55575302 | G | A | 1 | a0001c0002t0013g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1314+573G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575302 | |||||||
| chr16:55575346 | G | A | 263 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(260): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1314+617G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575346 | |||||||
| chr16:55575562 | A | G | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1314+833A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575562 | |||||||
| chr16:55575656 | C | T | 168 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(165): Show |
183 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1314+927C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575656 | |||||||
| chr16:55575680 | T | G | 83 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(80): Show |
94 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1314+951T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575680 | |||||||
| chr16:55575758 | T | C | 6 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0003c0004t0022g0022 others(3): Show |
7 | HG04115.hp2 NA18960.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1314+1029T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575758 | |||||||
| chr16:55575898 | A | C | 260 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(257): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1314+1169A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575898 | |||||||
| chr16:55575961 | C | A | 1 | a0002c0001t0048g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1314+1232C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575961 | |||||||
| chr16:55576185 | C | CT | 160 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(157): Show |
174 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.1314+1469dupT | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 55576185 | ||||||
| chr16:55576185 | C | CTT | 8 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0002c0001t0035g0163 others(5): Show |
9 | HG04115.hp2 NA18747.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.1314+1468_1314+146 others(6): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 55576185 | ||||||
| chr16:55576296 | A | G | 1 | a0002c0001t0048g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1314+1567A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55576296 | |||||||
| chr16:55576318 | G | A | 1 | a0002c0001t0013g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1314+1589G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55576318 | |||||||
| chr16:55576330 | T | C | 21 | a0001c0003t0010g0034 a0001c0003t0010g0036 a0001c0003t0010g0076 others(18): Show |
22 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1314+1601T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55576330 | |||||||
| chr16:55576416 | A | C | 2 | a0002c0001t0033g0092 a0002c0001t0033g0143 |
2 | HG01106.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1314+1687A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55576416 | |||||||
| chr16:55576446 | ATAGACTG others(42): Show |
A | 1 | a0002c0001t0033g0143 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1314+1724_1314+177 others(53): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 55576446 | ||||||
| chr16:55576454 | A | G | 167 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(164): Show |
182 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1314+1725A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55576454 | |||||||
| chr16:55576493 | G | T | 1 | a0002c0001t0005g0001 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1314+1764G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55576493 | |||||||
| chr16:55576616 | C | T | 11 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0003c0004t0022g0022 others(8): Show |
12 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.1314+1887C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55576616 | |||||||
| chr16:55576916 | G | A | 1 | a0002c0001t0033g0143 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1314+2187G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55576916 | |||||||
| chr16:55577049 | G | T | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1315-2060G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55577049 | |||||||
| chr16:55577309 | T | C | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1315-1800T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55577309 | |||||||
| chr16:55577312 | TG | T | 75 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0027 others(72): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1315-1795delG | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 55577312 | ||||||
| chr16:55577418 | T | C | 12 | a0001c0002t0046g0228 a0002c0001t0019g0142 a0002c0001t0032g0136 others(9): Show |
13 | HG00438.hp2 HG03491.hp2 HG03927.hp2 others(10): Show |
intron_variant | MODIFIER | c.1315-1691T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55577418 | |||||||
| chr16:55577973 | G | A | 4 | a0002c0001t0018g0018 a0002c0001t0018g0020 a0002c0001t0018g0120 others(1): Show |
5 | HG02723.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1315-1136G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55577973 | |||||||
| chr16:55578018 | G | A | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1315-1091G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55578018 | |||||||
| chr16:55578120 | T | C | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1315-989T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55578120 | |||||||
| chr16:55578365 | G | A | 166 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(163): Show |
181 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1315-744G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55578365 | |||||||
| chr16:55578702 | A | T | 20 | a0001c0002t0004g0214 a0001c0002t0009g0067 a0001c0002t0009g0068 others(17): Show |
22 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.1315-407A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55578702 | |||||||
| chr16:55578819 | T | C | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1315-290T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55578819 | |||||||
| chr16:55578881 | T | C | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1315-228T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55578881 | |||||||
| chr16:55579006 | T | A | 192 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(189): Show |
210 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1315-103T>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55579006 | |||||||
| chr16:55579032 | A | G | 1 | a0001c0002t0009g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1315-77A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55579032 | |||||||
| chr16:55579067 | A | G | 27 | a0001c0002t0005g0058 a0001c0002t0005g0202 a0002c0001t0005g0001 others(24): Show |
30 | HG00558.hp1 HG01099.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1315-42A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55579067 | |||||||
| chr16:55579266 | C | A | 1 | a0001c0002t0006g0196 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1450+22C>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55579266 | |||||||
| chr16:55579428 | T | C | 1 | a0002c0001t0024g0017 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1450+184T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55579428 | |||||||
| chr16:55579610 | A | G | 199 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(196): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.1450+366A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55579610 | |||||||
| chr16:55579753 | C | T | 1 | a0002c0001t0024g0017 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1450+509C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55579753 | |||||||
| chr16:55579939 | TGCACTGG others(6): Show |
T | 3 | a0002c0001t0009g0093 a0002c0001t0024g0090 a0002c0001t0027g0014 |
4 | HG02559.hp1 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+698_1450+710d others(15): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 55579939 | ||||||
| chr16:55580028 | T | G | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1450+784T>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580028 | |||||||
| chr16:55580054 | A | G | 3 | a0002c0001t0019g0091 a0005c0008t0015g0013 a0005c0008t0020g0013 |
3 | HG02809.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1450+810A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580054 | |||||||
| chr16:55580064 | T | C | 1 | a0003c0004t0077g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1450+820T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580064 | |||||||
| chr16:55580285 | G | A | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1450+1041G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580285 | |||||||
| chr16:55580320 | C | G | 1 | a0002c0001t0048g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1450+1076C>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580320 | |||||||
| chr16:55580535 | A | G | 169 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(166): Show |
184 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1450+1291A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580535 | |||||||
| chr16:55580691 | A | G | 7 | a0002c0001t0013g0029 a0002c0001t0014g0094 a0002c0001t0014g0095 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1450+1447A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580691 | |||||||
| chr16:55580780 | G | C | 4 | a0001c0002t0046g0228 a0003c0004t0022g0022 a0003c0004t0022g0023 others(1): Show |
5 | NA18960.hp1 NA18968.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1450+1536G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580780 | |||||||
| chr16:55580808 | T | C | 1 | a0002c0001t0002g0114 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1450+1564T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580808 | |||||||
| chr16:55580827 | T | C | 27 | a0001c0002t0005g0058 a0001c0002t0005g0202 a0002c0001t0005g0001 others(24): Show |
30 | HG00558.hp1 HG01099.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1450+1583T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580827 | |||||||
| chr16:55580833 | C | T | 3 | a0001c0003t0072g0210 a0002c0001t0033g0143 a0003c0004t0039g0187 |
3 | HG00438.hp2 HG01106.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1450+1589C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580833 | |||||||
| chr16:55580836 | A | ATTCTCAT others(2): Show |
157 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(154): Show |
171 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1450+1593_1450+159 others(13): Show |
LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 55580836 | ||||||
| chr16:55580838 | G | T | 157 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(154): Show |
171 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1450+1594G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580838 | |||||||
| chr16:55580839 | A | C | 157 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(154): Show |
171 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1450+1595A>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580839 | |||||||
| chr16:55580877 | G | T | 1 | a0001c0002t0003g0025 | 2 | HG00423.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1450+1633G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580877 | |||||||
| chr16:55580882 | T | C | 192 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(189): Show |
210 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1450+1638T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55580882 | |||||||
| chr16:55581388 | T | C | 1 | a0001c0003t0072g0210 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1451-1526T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55581388 | |||||||
| chr16:55581845 | T | C | 174 | a0001c0002t0002g0008 a0001c0002t0002g0033 a0001c0002t0003g0025 others(171): Show |
189 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1451-1069T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55581845 | |||||||
| chr16:55582064 | A | T | 3 | a0001c0002t0017g0219 a0001c0002t0017g0244 a0001c0002t0017g0247 |
3 | NA18967.hp2 NA18981.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1451-850A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55582064 | |||||||
| chr16:55582594 | T | C | 1 | a0002c0001t0008g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1451-320T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55582594 | |||||||
| chr16:55582869 | G | T | 1 | a0002c0005t0010g0021 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1451-45G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 13/13 | chr16 | 55582869 |