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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 544 | 157 | 27 | 35 | 63 | 6 | 25 | 44 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002 | 1/0 | 544 | 134 | 50 | 16 | 55 | 6 | 6 | 40 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0003 | 0/0 | 544 | 11 | 0 | 0 | 8 | 0 | 3 | 6 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0004 | 0/0 | 544 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0005 | 0/0 | 544 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0006 | 0/0 | 544 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0007 | 0/0 | 544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0008 | 0/0 | 544 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1635 | 129 | 46 | 16 | 54 | 6 | 6 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0002 | 0/1 | 1635 | 126 | 14 | 32 | 50 | 6 | 23 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0003 | 0/0 | 1635 | 30 | 13 | 2 | 13 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0004 | 0/0 | 1635 | 10 | 0 | 0 | 7 | 0 | 3 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0005 | 0/0 | 1635 | 5 | 4 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0006 | 0/0 | 1635 | 4 | 4 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0007 | 0/0 | 1635 | 4 | 0 | 2 | 0 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0008 | 0/0 | 1635 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0009 | 0/0 | 1635 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0010 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0011 | 0/0 | 1635 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
c0012 | 0/0 | 1635 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3679 | 44 | 1 | 20 | 13 | 3 | 6 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0002 | 0/0 | 3675 | 22 | 3 | 5 | 8 | 3 | 3 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0003 | 0/0 | 3675 | 19 | 7 | 4 | 4 | 2 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0004 | 0/0 | 3679 | 18 | 1 | 3 | 11 | 1 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0005 | 0/0 | 3741 | 18 | 0 | 4 | 13 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0006 | 0/0 | 3675 | 15 | 2 | 1 | 7 | 1 | 4 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0007 | 0/0 | 3741 | 12 | 1 | 3 | 6 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0008 | 0/0 | 3671 | 11 | 4 | 1 | 3 | 0 | 3 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0009 | 0/0 | 3679 | 9 | 2 | 2 | 2 | 0 | 3 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0010 | 0/0 | 3679 | 9 | 4 | 1 | 3 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0011 | 0/0 | 3679 | 9 | 3 | 0 | 6 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0012 | 0/0 | 3675 | 7 | 0 | 1 | 6 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0013 | 1/0 | 3679 | 6 | 1 | 0 | 3 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0014 | 0/0 | 3678 | 6 | 6 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0015 | 0/0 | 3679 | 5 | 1 | 0 | 4 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0016 | 0/0 | 3671 | 5 | 5 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0017 | 0/0 | 3741 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0018 | 0/0 | 3741 | 4 | 4 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0019 | 0/0 | 3679 | 4 | 1 | 1 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0020 | 0/0 | 3679 | 4 | 1 | 1 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0021 | 0/0 | 3741 | 4 | 3 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0022 | 0/0 | 3679 | 4 | 0 | 0 | 3 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0023 | 0/0 | 3682 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0024 | 0/0 | 3741 | 3 | 1 | 0 | 0 | 2 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0025 | 0/0 | 3675 | 3 | 0 | 2 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0026 | 0/0 | 3679 | 2 | 0 | 2 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0027 | 0/0 | 3737 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0028 | 0/0 | 3678 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0029 | 0/0 | 3675 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0030 | 0/0 | 3679 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0031 | 0/0 | 3679 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0032 | 0/0 | 3679 | 2 | 0 | 0 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0033 | 0/0 | 3741 | 2 | 1 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0034 | 0/0 | 3737 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0035 | 0/0 | 3737 | 2 | 0 | 0 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0036 | 0/0 | 3737 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0037 | 0/0 | 3675 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0038 | 0/0 | 3679 | 2 | 1 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0039 | 0/0 | 3679 | 2 | 0 | 0 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0040 | 0/0 | 3741 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0041 | 0/0 | 3675 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0042 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0043 | 0/0 | 3741 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0044 | 0/0 | 3675 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0045 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0046 | 0/0 | 3741 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0047 | 0/0 | 3741 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0048 | 0/0 | 3741 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0049 | 0/0 | 3741 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0050 | 0/0 | 3741 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0051 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0052 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0053 | 0/0 | 3675 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0054 | 0/0 | 3675 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0055 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0056 | 0/0 | 3675 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0057 | 0/0 | 3741 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0058 | 0/0 | 3675 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0059 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0060 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0061 | 0/0 | 3741 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0062 | 0/0 | 3675 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0063 | 0/0 | 3679 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0064 | 0/0 | 3675 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0065 | 0/0 | 3737 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0066 | 0/0 | 3675 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0067 | 0/0 | 3737 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0068 | 0/0 | 3674 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0069 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0070 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0071 | 0/0 | 3741 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0072 | 0/0 | 3741 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0073 | 0/0 | 3675 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0074 | 0/0 | 3679 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0075 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0076 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
t0077 | 0/0 | 3679 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0002 | 0/0 | 5 | 0 | 2 | 0 | 3 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0004 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0007 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0008 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0010 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/1 | 1635 | 126 | 14 | 32 | 50 | 6 | 23 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003 | 0/0 | 1635 | 30 | 13 | 2 | 13 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0011 | 0/0 | 1635 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001 | 1/0 | 1635 | 129 | 46 | 16 | 54 | 6 | 6 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0005 | 0/0 | 1635 | 5 | 4 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0003c0004 | 0/0 | 1635 | 10 | 0 | 0 | 7 | 0 | 3 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0003c0010 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0004c0006 | 0/0 | 1635 | 4 | 4 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0005c0007 | 0/0 | 1635 | 4 | 0 | 2 | 0 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0006c0008 | 0/0 | 1635 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0007c0009 | 0/0 | 1635 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0008c0012 | 0/0 | 1635 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | 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 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0002 | 0/0 | 5309 | 3 | 0 | 0 | 1 | 1 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0003 | 0/0 | 5309 | 4 | 0 | 2 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0004 | 0/0 | 5313 | 18 | 1 | 3 | 11 | 1 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0005 | 0/0 | 5375 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0006 | 0/0 | 5309 | 7 | 1 | 0 | 1 | 1 | 4 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0007 | 0/0 | 5375 | 12 | 1 | 3 | 6 | 0 | 2 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0008 | 0/0 | 5305 | 3 | 0 | 0 | 0 | 0 | 3 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0009 | 0/0 | 5313 | 6 | 1 | 2 | 0 | 0 | 3 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0013 | 0/0 | 5313 | 4 | 0 | 0 | 3 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0014 | 0/0 | 5312 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0016 | 0/0 | 5305 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0017 | 0/0 | 5375 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0025 | 0/0 | 5309 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0026 | 0/0 | 5313 | 2 | 0 | 2 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0029 | 0/0 | 5309 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0031 | 0/0 | 5313 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0035 | 0/0 | 5371 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0036 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0040 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0042 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0043 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0044 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0046 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0002t0050 | 0/0 | 5375 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0010 | 0/0 | 5313 | 6 | 1 | 1 | 3 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0011 | 0/0 | 5313 | 8 | 3 | 0 | 5 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0021 | 0/0 | 5375 | 4 | 3 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0034 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0037 | 0/0 | 5309 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0038 | 0/0 | 5313 | 2 | 1 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0059 | 0/0 | 5312 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0060 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0069 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0070 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0071 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0003t0072 | 0/0 | 5375 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0001c0011t0001 | 0/0 | 5313 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0002 | 0/0 | 5309 | 17 | 3 | 4 | 7 | 2 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0003 | 0/0 | 5309 | 14 | 7 | 2 | 2 | 2 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0005 | 0/0 | 5375 | 16 | 0 | 4 | 11 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0006 | 0/0 | 5309 | 8 | 1 | 1 | 6 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0008 | 0/0 | 5305 | 7 | 4 | 0 | 3 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0009 | 0/0 | 5313 | 3 | 1 | 0 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0012 | 0/0 | 5309 | 7 | 0 | 1 | 6 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0013 | 1/0 | 5313 | 2 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0014 | 0/0 | 5312 | 4 | 4 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0015 | 0/0 | 5313 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0016 | 0/0 | 5305 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0018 | 0/0 | 5375 | 4 | 4 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0019 | 0/0 | 5313 | 4 | 1 | 1 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0020 | 0/0 | 5313 | 3 | 0 | 1 | 2 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0024 | 0/0 | 5375 | 3 | 1 | 0 | 0 | 2 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0025 | 0/0 | 5309 | 2 | 0 | 1 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0027 | 0/0 | 5371 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0028 | 0/0 | 5312 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0030 | 0/0 | 5313 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0032 | 0/0 | 5313 | 2 | 0 | 0 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0033 | 0/0 | 5375 | 2 | 1 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0035 | 0/0 | 5371 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0048 | 0/0 | 5375 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0049 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0051 | 0/0 | 5312 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0052 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0053 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0054 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0055 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0056 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0057 | 0/0 | 5375 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0058 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0061 | 0/0 | 5375 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0062 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0064 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0065 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0066 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0067 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0068 | 0/0 | 5308 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0001t0073 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0005t0010 | 0/0 | 5313 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0005t0011 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0002c0005t0063 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0003c0004t0022 | 0/0 | 5313 | 4 | 0 | 0 | 3 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0003c0004t0039 | 0/0 | 5313 | 2 | 0 | 0 | 1 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0003c0004t0045 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0003c0004t0074 | 0/0 | 5313 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0003c0004t0075 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0003c0004t0077 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0003c0010t0076 | 0/0 | 5313 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0004c0006t0023 | 0/0 | 5316 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0004c0006t0047 | 0/0 | 5375 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0005c0007t0002 | 0/0 | 5309 | 2 | 0 | 1 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0005c0007t0003 | 0/0 | 5309 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0005c0007t0008 | 0/0 | 5305 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0006c0008t0015 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0006c0008t0020 | 0/0 | 5313 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0007c0009t0014 | 0/0 | 5312 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
a0008c0012t0041 | 0/0 | 5309 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | copy fasta | chr16 | 55504072 | 55591666 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0002 | 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 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0246 | 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 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0264 | 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 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0001g0270 | 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 |
a0001c0002t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0004g0002 | 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 |
a0001c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0004g0260 | 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 |
a0001c0002t0005g0203 | 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 |
a0001c0002t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0006g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0006g0200 | 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 |
a0001c0002t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0007g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0007g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0007g0263 | 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 |
a0001c0002t0008g0204 | 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 |
a0001c0002t0017g0220 | 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 |
a0001c0002t0017g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0017g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0025g0199 | 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 |
a0001c0002t0026g0226 | 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 |
a0001c0002t0035g0198 | 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 |
a0001c0002t0040g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0042g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0043g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0044g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0002t0046g0229 | 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 |
a0001c0003t0010g0209 | 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 |
a0001c0003t0011g0210 | 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 |
a0001c0003t0037g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0003t0037g0208 | 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 |
a0001c0003t0069g0196 | 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 |
a0001c0003t0072g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0001c0011t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0002g0001 | 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 |
a0002c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0003g0001 | 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 |
a0002c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0005g0003 | 0/0 | 2 | 0 | 1 | 1 | 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 |
a0002c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0005g0181 | 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 |
a0002c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0008g0001 | 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 |
a0002c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0008g0174 | 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 |
a0002c0001t0013g0148 | 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 |
a0002c0001t0014g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0014g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0015g0003 | 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 |
a0002c0001t0015g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0015g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0016g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0016g0194 | 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 |
a0002c0001t0019g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0019g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0019g0152 | 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 |
a0002c0001t0020g0180 | 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 |
a0002c0001t0025g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0025g0159 | 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 |
a0002c0001t0028g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0028g0177 | 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 |
a0002c0001t0032g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0032g0153 | 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 |
a0002c0001t0033g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0035g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0048g0167 | 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 |
a0002c0001t0053g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0054g0145 | 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 |
a0002c0001t0056g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0057g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0058g0186 | 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 |
a0002c0001t0062g0003 | 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 |
a0002c0001t0065g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0066g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0067g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0068g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0001t0073g0163 | 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 |
a0002c0005t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0005t0011g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0002c0005t0063g0168 | 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 |
a0003c0004t0022g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0003c0004t0039g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0003c0004t0039g0188 | 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 |
a0003c0004t0074g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0003c0004t0075g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0003c0004t0077g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0003c0010t0076g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0004c0006t0023g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0004c0006t0023g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0004c0006t0023g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0004c0006t0047g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0005c0007t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0005c0007t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0005c0007t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0005c0007t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0006c0008t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
a0006c0008t0020g0013 | 0/0 | 1 | 1 | 0 | 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 |
a0008c0012t0041g0224 | 0/0 | 1 | 0 | 1 | 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 | g0002 | 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 | g0002 | 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 | g0242 | 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 | g0188 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG00558 | hp1 | a0002 | c0001 | t0062 | g0003 | 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 | g0227 | EAS | CHS | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG00597 | hp2 | a0001 | c0003 | t0037 | g0208 | 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 | g0158 | 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 | g0240 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0270 | 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 | g0226 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG00741 | hp1 | a0002 | c0001 | t0003 | g0202 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0222 | 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 | g0262 | 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 | g0002 | 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 | g0232 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01099 | hp1 | a0002 | c0001 | t0005 | g0179 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0267 | 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 | g0144 | 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 | a0005 | c0007 | t0002 | g0183 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01168 | hp1 | a0002 | c0001 | t0006 | g0176 | 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 | g0264 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01175 | hp2 | a0002 | c0001 | t0005 | g0150 | 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 | g0201 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01243 | hp1 | a0002 | c0001 | t0020 | g0180 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0205 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01257 | hp2 | a0008 | c0012 | t0041 | g0224 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01261 | hp2 | a0001 | c0002 | t0007 | g0263 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01358 | hp1 | a0001 | c0011 | t0001 | g0265 | 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 | g0199 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01433 | hp2 | a0005 | c0007 | t0008 | g0182 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01496 | hp1 | a0002 | c0001 | t0005 | g0003 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0230 | 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 | g0002 | 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 | g0178 | 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 | g0219 | 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 | g0225 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01952 | hp2 | a0002 | c0001 | t0019 | g0152 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01975 | hp1 | a0002 | c0001 | t0005 | g0155 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02004 | hp1 | a0001 | c0002 | t0007 | g0216 | AMR | PEL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02004 | hp2 | a0002 | c0001 | t0025 | g0159 | 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 | g0252 | 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 | g0001 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02074 | hp2 | a0001 | c0003 | t0010 | g0209 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02080 | hp1 | a0001 | c0002 | t0042 | g0228 | 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 | g0207 | EAS | KHV | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02083 | hp2 | a0002 | c0001 | t0073 | g0163 | 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 | g0237 | 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 | g0142 | EAS | CDX | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02165 | hp2 | a0002 | c0001 | t0019 | g0141 | EAS | CDX | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02257 | hp1 | a0002 | c0001 | t0003 | g0161 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02257 | hp2 | a0002 | c0005 | t0010 | g0175 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02258 | hp1 | a0002 | c0001 | t0003 | g0173 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02258 | hp2 | a0002 | c0005 | t0063 | g0168 | 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 | g0255 | 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 | g0149 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02572 | hp1 | a0002 | c0001 | t0028 | g0177 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02572 | hp2 | a0004 | c0006 | t0047 | g0012 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02602 | hp1 | a0001 | c0002 | t0035 | g0198 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0254 | 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 | g0167 | 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 | g0146 | AFR | GWD | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02647 | hp1 | a0004 | 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 | g0259 | 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 | g0269 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02698 | hp2 | a0002 | c0001 | t0057 | g0130 | 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 | g0215 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02735 | hp2 | a0005 | c0007 | t0003 | g0185 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG02738 | hp2 | a0001 | c0002 | t0006 | g0200 | 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 | a0006 | 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 | a0006 | 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 | g0001 | 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 | g0218 | 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 | g0138 | 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 | g0212 | 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 | g0211 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG03139 | hp1 | a0002 | c0001 | t0065 | g0135 | 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 | a0004 | c0006 | t0023 | g0089 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG03209 | hp1 | a0004 | 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 | g0147 | 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 | g0186 | 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 | g0238 | SAS | PJL | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG03491 | hp2 | a0003 | c0004 | t0074 | g0189 | 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 | g0172 | AFR | ESN | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG03579 | hp1 | a0002 | c0001 | t0002 | g0001 | 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 | g0204 | 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 | g0197 | 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 | g0213 | SAS | BEB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG03942 | hp1 | a0003 | c0004 | t0039 | g0187 | SAS | BEB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG03942 | hp2 | a0001 | c0002 | t0004 | g0260 | 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 | g0143 | SAS | STU | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG04199 | hp1 | a0005 | c0007 | t0002 | g0184 | 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 | g0137 | 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 | g0192 | EAS | CHB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18906 | hp1 | a0002 | c0001 | t0003 | g0157 | 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 | g0203 | 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 | g0136 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18945 | hp1 | a0002 | c0001 | t0015 | g0003 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18945 | hp2 | a0001 | c0002 | t0004 | g0223 | 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 | g0236 | 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 | g0001 | 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 | g0246 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18952 | hp2 | a0001 | c0003 | t0011 | g0210 | 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 | g0196 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18956 | hp2 | a0002 | c0001 | t0005 | g0129 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18957 | hp1 | a0001 | c0002 | t0004 | g0217 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18957 | hp2 | a0002 | c0001 | t0002 | g0162 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18960 | hp1 | a0001 | c0002 | t0046 | g0229 | 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 | g0151 | 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 | g0244 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18966 | hp1 | a0002 | c0001 | t0005 | g0131 | 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 | g0001 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18967 | hp2 | a0001 | c0002 | t0017 | g0248 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18968 | hp1 | a0002 | c0001 | t0003 | g0166 | 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 | g0235 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18972 | hp2 | a0002 | c0001 | t0035 | g0164 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18973 | hp1 | a0002 | c0001 | t0005 | g0181 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0239 | 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 | g0261 | 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 | g0191 | 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 | g0132 | 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 | g0165 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18981 | hp2 | a0001 | c0002 | t0017 | g0220 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18982 | hp2 | a0002 | c0001 | t0066 | g0139 | 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 | g0231 | 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 | g0171 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18992 | hp1 | a0001 | c0002 | t0004 | g0243 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18992 | hp2 | a0002 | c0001 | t0005 | g0003 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18993 | hp1 | a0003 | c0004 | t0075 | g0190 | 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 | g0133 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA18995 | hp2 | a0001 | c0002 | t0044 | g0247 | 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 | g0193 | 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 | g0251 | 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 | g0153 | 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 | g0140 | AFR | LWK | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA19030 | hp2 | a0002 | c0001 | t0054 | g0145 | 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 | g0169 | 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 | g0257 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA19059 | hp1 | a0001 | c0002 | t0006 | g0195 | 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 | g0154 | EAS | JPT | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA19060 | hp2 | a0001 | c0002 | t0007 | g0234 | 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 | g0245 | 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 | g0258 | 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 | g0134 | 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 | g0156 | 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 | g0233 | EUR | TSI | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA20752 | hp2 | a0002 | c0001 | t0003 | g0170 | EUR | TSI | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0253 | 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 | g0266 | AMR | CLM | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0206 | 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 | g0174 | AFR | ACB | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
HG03471 | hp1 | a0002 | c0001 | t0002 | g0160 | 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 | g0194 | 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 | hp1 | a0001 | c0002 | t0001 | g0048 | REF | REF | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
homoSapiens_grch38 | hp1 | a0002 | c0001 | t0013 | g0148 | REF | REF | LPCAT2_chr16_55504072_55591666 | LPCAT2 | chr16 | 55504072 | 55591666 |
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 | a0008 | 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 | a0004 | 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 | a0005 | 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 | a0001a0007a0008 | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(156): 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 | a0006 | 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 |
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 | a0001c0003a0002c0005a0003c0010 | 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 |
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 | a0003c0004t0022a0003c0004t0039a0003c0004t0074others(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 | a0001c0002t0001a0001c0002t0004a0001c0002t0007others(10): Show | 87 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(84): 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 | a0001c0002t0002a0001c0002t0003a0001c0002t0005others(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 | a0001c0002t0002a0001c0002t0003a0001c0002t0005others(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 | a0002c0001t0018a0002c0001t0055 | 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 | a0004c0006t0023a0004c0006t0047 | 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 | a0001c0002t0002a0001c0002t0003a0001c0002t0005others(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 | a0001c0003t0010a0001c0003t0011a0001c0003t0021others(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 | a0001c0002t0002a0001c0002t0003a0001c0002t0006others(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 | a0001c0002t0040a0001c0003t0069a0001c0003t0070others(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 | a0001c0002t0003a0001c0002t0016a0001c0002t0025others(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 | a0001c0003t0034a0002c0001t0067a0002c0005t0063 | 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 | a0001c0002t0050a0001c0003t0072a0002c0001t0033others(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 | a0001c0002t0008a0001c0002t0016a0001c0002t0029others(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 | a0001c0002t0005a0001c0002t0007a0001c0002t0017others(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 | a0001c0002t0005a0001c0002t0007a0001c0002t0017others(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 | a0001c0002t0004a0001c0002t0005a0001c0002t0006others(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 | a0001c0002t0005a0001c0002t0007a0001c0002t0017others(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 | a0002c0001t0028a0002c0001t0051 | 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 | a0001c0002t0005a0001c0002t0007a0001c0002t0017others(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 | a0004c0006t0023 | 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 | a0004c0006t0023 | 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 | a0001c0002t0014a0001c0003t0059a0002c0001t0014others(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 | a0001c0002t0036a0002c0001t0027 | 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 | a0001c0002t0005a0001c0002t0007a0001c0002t0017others(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 |
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 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(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 | a0001c0002t0001g0262a0001c0002t0001g0264a0001c0002t0001g0266others(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 | a0003c0004t0022g0213 | 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 | a0002c0001t0003g0212 | 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 | a0001c0003t0072g0211 | 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 | a0001c0003t0010g0209a0001c0003t0011g0210 | 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 | a0001c0002t0002g0008a0001c0002t0003g0025a0001c0002t0003g0205others(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 | 123 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(120): Show | 134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.171+383G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55509735 | ||||||
chr16:55509966
|
T | C | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0001c0003t0037g0207a0001c0003t0037g0208a0002c0001t0002g0193others(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 | a0001c0002t0001g0214a0001c0002t0001g0262a0001c0002t0004g0215others(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 |
79 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(76): Show | 90 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(87): 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 | a0001c0002t0001g0252a0001c0002t0001g0253a0001c0002t0001g0254others(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 | a0001c0002t0007g0261 | 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 | a0001c0002t0009g0067a0001c0002t0009g0068a0001c0002t0009g0069others(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 | a0001c0002t0009g0074a0001c0002t0031g0073a0001c0002t0031g0075 | 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 | a0001c0003t0010g0076a0001c0003t0010g0077a0001c0003t0060g0078 | 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 | a0001c0002t0006g0195a0002c0001t0005g0085a0002c0001t0005g0087others(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 | a0001c0002t0004g0218 | 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 | a0003c0004t0022g0213a0003c0004t0039g0187a0003c0004t0039g0188others(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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0002c0001t0009g0093a0002c0001t0019g0091a0002c0001t0024g0090others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | 147 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(144): Show | 161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): 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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0014g0094others(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 | a0001c0002t0002g0033a0001c0002t0005g0058a0001c0002t0009g0067others(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 | a0001c0003t0010g0063a0001c0003t0011g0061a0001c0003t0021g0056others(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 | 152 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(149): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.171+2343G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55511695 | ||||||
chr16:55511700
|
A | G | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0045g0022others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0003c0004t0077g0192 | 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 | a0002c0001t0009g0093a0002c0001t0019g0091a0002c0001t0024g0090others(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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0002c0001t0009g0093a0002c0001t0019g0091a0002c0001t0024g0090others(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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0001c0002t0004g0251 | 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 | a0001c0002t0016g0045a0001c0002t0050g0044a0001c0003t0034g0031others(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 | a0001c0002t0006g0082a0001c0002t0016g0081 | 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 | a0001c0002t0004g0260 | 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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0002c0001t0058g0186 | 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 | 134 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(131): Show | 147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): 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 | a0001c0002t0001g0250 | 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0003c0004t0022g0213a0003c0004t0039g0187a0003c0004t0039g0188others(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 | a0001c0003t0069g0196 | 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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0045g0022others(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 | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0013g0029others(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 | a0001c0003t0011g0210 | 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 | a0001c0003t0010g0063a0001c0003t0011g0061a0001c0003t0021g0056others(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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0214others(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 | 36 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(33): Show | 38 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(35): 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 | a0001c0002t0001g0027a0001c0002t0001g0054a0001c0002t0001g0242others(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 | a0001c0002t0001g0246a0001c0002t0001g0249a0001c0002t0001g0262others(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 | a0001c0003t0010g0063a0001c0003t0021g0062a0001c0003t0021g0064others(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 | a0001c0002t0001g0221a0001c0002t0001g0252a0001c0002t0006g0024others(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 | a0001c0002t0002g0033a0001c0002t0005g0058a0001c0002t0009g0067others(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 | a0001c0002t0014g0080a0001c0002t0016g0081a0002c0001t0012g0101others(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 | a0001c0002t0006g0082a0001c0002t0016g0084a0001c0002t0036g0011others(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 | a0002c0001t0018g0018a0002c0001t0018g0020a0002c0001t0018g0120others(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 | a0001c0002t0001g0262 | 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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0001c0002t0006g0082a0001c0002t0014g0080a0001c0002t0016g0081others(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 | a0002c0001t0018g0018a0002c0001t0018g0020a0002c0001t0018g0120others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | 88 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(85): Show | 99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): 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 | a0003c0004t0077g0192 | 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 | a0001c0002t0016g0045a0001c0002t0050g0044a0001c0003t0034g0031others(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 | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0001c0002t0016g0084a0001c0002t0036g0011 | 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 | a0001c0002t0006g0082a0001c0002t0016g0081 | 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 | 147 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(144): Show | 161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): 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 | a0003c0004t0077g0192 | 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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0002c0001t0003g0166 | 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 | a0002c0001t0002g0162a0002c0001t0002g0165a0002c0001t0002g0193others(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 | 75 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(72): Show | 86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): 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 | a0003c0004t0077g0192 | 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 | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0001c0002t0001g0253a0001c0002t0001g0256a0001c0002t0001g0262others(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 | a0001c0002t0006g0082a0001c0002t0016g0081 | 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 | 80 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(77): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): 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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0001c0002t0013g0040a0001c0002t0013g0041 | 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 | a0001c0002t0001g0269a0001c0002t0007g0263 | 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0001c0003t0010g0209a0001c0003t0011g0210 | 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 | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0001c0002t0002g0033a0001c0002t0005g0058a0001c0002t0009g0067others(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 | a0005c0007t0003g0185 | 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 | a0001c0002t0016g0045a0001c0002t0050g0044a0001c0003t0034g0031others(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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0002c0001t0002g0160a0002c0001t0003g0161 | 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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0013g0029others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0001c0003t0010g0063a0001c0003t0011g0061a0001c0003t0021g0056others(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 | a0001c0002t0006g0082a0001c0002t0014g0080a0001c0002t0016g0081others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0001c0002t0001g0259 | 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 | a0002c0001t0025g0159 | 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 | 152 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(149): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.172-6269A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519239 | ||||||
chr16:55519246
|
G | A | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.172-6262G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519246 | ||||||
chr16:55519270
|
G | C | 1 | a0001c0002t0001g0048 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.172-6238G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519270 | ||||||
chr16:55519276
|
G | A | 11 | a0002c0001t0008g0169a0003c0004t0022g0022a0003c0004t0022g0023others(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 | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0001c0002t0001g0214a0001c0003t0011g0030a0001c0003t0011g0043others(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 | a0001c0002t0001g0047a0001c0002t0001g0221a0001c0003t0038g0065others(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 | a0002c0001t0009g0093a0002c0001t0019g0091a0002c0001t0024g0090others(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 | 122 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(119): Show | 134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): 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 | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.172-5988G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55519520 | ||||||
chr16:55519548
|
A | G | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0003c0004t0077g0192 | 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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0014g0094others(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 | a0001c0002t0006g0082a0001c0002t0016g0081 | 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0002c0001t0003g0166 | 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 | a0002c0001t0002g0158 | 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 | 76 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(73): Show | 87 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.172-4718C>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55520790 | ||||||
chr16:55520825
|
C | T | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0045g0022others(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 | a0001c0002t0016g0084a0001c0002t0036g0011a0007c0009t0014g0083 | 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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.172-4385G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55521123 | ||||||
chr16:55521365
|
G | A | 152 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(149): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(163): 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0002c0001t0008g0096a0002c0001t0008g0097 | 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 | a0001c0003t0010g0063a0001c0003t0011g0061a0001c0003t0021g0056others(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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0014g0094others(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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0001c0002t0001g0266a0001c0002t0001g0270 | 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 | 7 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0051others(4): Show | 7 | HG00639.hp2 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-1660G>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 1/13 | chr16 | 55523848 | ||||||
chr16:55523849
|
G | A | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | 126 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(123): Show | 138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): 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 | a0002c0001t0018g0018a0002c0001t0018g0020a0002c0001t0018g0120others(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 | a0001c0002t0007g0234 | 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 | a0001c0002t0007g0234 | 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 | a0002c0001t0003g0157 | 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 | 80 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(77): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): 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 | a0001c0002t0004g0009a0001c0002t0007g0009a0001c0002t0007g0234others(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 | 147 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(144): Show | 161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): 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 | a0002c0001t0002g0156 | 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 | 135 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(132): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): 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 | a0001c0002t0016g0045a0001c0002t0050g0044a0001c0003t0034g0031others(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 | 88 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(85): Show | 99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): 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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0001c0002t0001g0256a0001c0002t0004g0223 | 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 | a0001c0002t0001g0269a0001c0002t0007g0263 | 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 | 80 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(77): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): 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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0022g0213others(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 | a0001c0002t0003g0206 | 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 | a0001c0002t0016g0045a0001c0003t0034g0031a0001c0003t0034g0046 | 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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0013g0029others(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 | a0003c0004t0022g0022a0003c0004t0022g0023a0003c0004t0045g0022others(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 | 158 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(155): Show | 173 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(170): 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 | a0001c0002t0016g0084a0001c0002t0036g0011a0007c0009t0014g0083 | 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 | a0002c0001t0005g0155 | 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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | 128 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(125): Show | 140 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.312-1222A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55527155 | ||||||
chr16:55527168
|
T | C | 138 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(135): Show | 151 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(148): 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0002c0001t0048g0167a0002c0005t0063g0168 | 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 | a0001c0002t0002g0033a0001c0002t0005g0058a0001c0002t0009g0067others(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 | a0001c0002t0003g0205a0001c0003t0010g0063a0001c0003t0011g0061others(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 | a0001c0002t0002g0033a0001c0002t0005g0058a0001c0002t0009g0067others(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 | a0001c0002t0008g0204 | 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 | a0001c0002t0006g0082a0001c0002t0016g0081 | 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 | 154 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(151): Show | 168 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(165): 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 | a0001c0002t0002g0033a0001c0002t0005g0058a0001c0002t0009g0067others(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 | 275 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(272): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.312-32G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 2/13 | chr16 | 55528345 | ||||||
chr16:55528660
|
T | C | 30 | a0002c0001t0002g0121a0002c0001t0002g0122a0002c0001t0002g0158others(27): 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 | a0001c0002t0016g0084a0001c0002t0036g0011a0007c0009t0014g0083 | 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 | a0001c0002t0007g0236a0001c0002t0040g0235 | 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 | a0002c0001t0002g0193a0002c0001t0006g0015a0002c0001t0006g0108others(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 | 136 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(133): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): 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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014others(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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0001c0002t0009g0067a0001c0002t0009g0070 | 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 | 137 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(134): Show | 150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): 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 | a0001c0003t0010g0063a0001c0003t0011g0061a0001c0003t0021g0056others(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 | 114 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(111): Show | 126 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(123): 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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0014g0094others(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 | 134 | a0001c0002t0001g0222a0001c0002t0001g0246a0001c0002t0002g0008others(131): 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 | a0002c0001t0018g0018a0002c0001t0018g0020a0002c0001t0018g0120others(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 | a0001c0002t0003g0206a0001c0002t0006g0024a0001c0002t0009g0067others(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 | 134 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(131): Show | 147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0001c0002t0001g0233a0001c0002t0004g0215 | 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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0001c0003t0072g0211 | 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 | a0001c0002t0009g0067a0001c0002t0009g0068a0001c0002t0009g0069others(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 | a0002c0001t0005g0154 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0016g0084a0001c0002t0036g0011 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0002c0001t0002g0016a0002c0001t0003g0007a0002c0001t0006g0176 | 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 | a0002c0001t0019g0141a0002c0001t0056g0142 | 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 | a0002c0001t0024g0017a0002c0001t0030g0019a0002c0001t0033g0144 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0002c0001t0003g0170 | 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 | a0001c0002t0016g0084a0001c0002t0036g0011 | 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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | 233 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(230): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): 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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0002c0001t0054g0145 | 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 | a0002c0001t0015g0171 | 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 | a0001c0003t0010g0063a0001c0003t0011g0030a0001c0003t0021g0060others(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 | a0001c0002t0006g0195a0002c0001t0002g0117a0002c0001t0002g0165others(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 | a0002c0001t0019g0143a0003c0004t0022g0023a0003c0004t0039g0188others(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 | a0001c0002t0006g0082a0001c0002t0016g0045a0001c0002t0016g0081others(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 | a0001c0002t0009g0069a0001c0002t0013g0040a0001c0002t0013g0066others(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 | a0001c0002t0009g0067a0001c0002t0009g0068a0001c0002t0009g0070others(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 | 92 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0047others(89): Show | 105 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(102): 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 | a0001c0002t0016g0084a0001c0002t0036g0011 | 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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | 76 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(73): Show | 87 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(84): 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 | a0001c0003t0010g0063a0001c0003t0011g0061a0001c0003t0021g0060others(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 | 268 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(265): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): 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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0001c0002t0009g0067a0001c0002t0009g0068a0001c0002t0009g0069others(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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0001c0002t0001g0262a0001c0002t0001g0264a0001c0002t0001g0266others(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 | a0003c0004t0039g0188 | 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 | a0003c0004t0077g0192 | 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 | a0003c0004t0022g0213a0003c0004t0039g0187a0003c0004t0039g0188others(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 | a0001c0003t0010g0063a0001c0003t0011g0030a0001c0003t0011g0043others(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 | a0001c0002t0009g0067a0001c0002t0009g0068a0001c0002t0009g0069others(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 | a0002c0001t0006g0176 | 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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0001c0002t0001g0233a0001c0002t0004g0215 | 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 | a0001c0002t0006g0195 | 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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | 204 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(201): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): 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 | a0003c0004t0077g0192 | 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 | a0001c0002t0001g0221a0001c0002t0001g0225a0001c0002t0004g0219 | 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 | a0002c0001t0018g0018a0002c0001t0018g0020a0002c0001t0018g0120others(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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0002c0001t0008g0169 | 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 | a0001c0002t0001g0221 | 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 | 188 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(185): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): 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 | a0005c0007t0002g0184 | 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 | a0001c0002t0001g0259 | 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 | a0001c0003t0010g0209 | 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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0001c0002t0026g0226 | 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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0001c0002t0016g0084a0001c0002t0036g0011 | 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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0001c0002t0001g0256a0001c0002t0001g0259a0001c0002t0001g0264others(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 | 183 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(180): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): 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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0002c0001t0012g0102a0002c0001t0012g0103a0002c0001t0012g0106 | 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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0001c0002t0006g0082a0001c0002t0008g0026a0001c0002t0008g0204others(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 | 198 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(195): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): 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 | a0001c0002t0006g0082a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | 268 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(265): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): 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 | a0001c0002t0009g0067a0001c0002t0009g0068a0001c0002t0009g0069others(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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0014g0094others(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 | a0001c0002t0016g0045a0001c0002t0050g0044a0001c0003t0034g0031others(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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0013g0029others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | 197 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(194): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): 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 | a0001c0002t0013g0037a0001c0002t0013g0040a0001c0002t0013g0041others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0002c0001t0012g0102a0002c0001t0012g0103a0002c0001t0012g0106 | 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 | 27 | a0001c0002t0005g0058a0001c0002t0005g0203a0001c0002t0006g0195others(24): 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 | a0001c0002t0001g0233a0001c0002t0004g0215 | 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 | 68 | a0001c0002t0001g0246a0001c0002t0005g0058a0001c0002t0005g0203others(65): 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 | a0002c0001t0002g0165a0002c0001t0035g0164 | 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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0013g0029others(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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0001c0002t0007g0263 | 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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | 196 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(193): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0004g0218 | 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 | 188 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(185): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0001g0253a0001c0002t0001g0256a0001c0002t0001g0262others(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 | a0002c0001t0002g0116a0002c0001t0066g0139 | 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 | a0003c0004t0077g0192 | 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 | a0003c0004t0022g0213a0003c0004t0039g0187a0003c0004t0039g0188others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0001g0232 | 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 | 259 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(256): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): 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 | a0001c0002t0004g0219 | 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 | a0001c0002t0016g0045a0001c0002t0050g0044a0001c0003t0034g0031others(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 | a0001c0002t0003g0205a0001c0002t0006g0197a0001c0002t0025g0199 | 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 | a0004c0006t0023g0089 | 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 | a0001c0002t0013g0037a0001c0002t0013g0040a0001c0002t0013g0041others(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 | a0001c0002t0009g0067a0001c0002t0009g0068a0001c0002t0009g0069others(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 | a0002c0001t0002g0160a0002c0001t0003g0161 | 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 | a0003c0004t0077g0192 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | 188 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(185): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): 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 | a0001c0002t0001g0256 | 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 | 188 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(185): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): 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 | a0001c0002t0001g0262a0001c0002t0001g0267a0001c0002t0001g0268others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0001c0003t0010g0063a0001c0003t0011g0030a0001c0003t0011g0043others(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 | a0002c0001t0016g0194 | 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 | a0002c0001t0002g0165a0002c0001t0035g0164 | 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 | a0002c0001t0003g0126a0002c0001t0065g0135a0002c0001t0067g0140 | 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 | a0001c0002t0009g0067a0001c0002t0009g0070 | 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 | a0002c0001t0018g0018a0002c0001t0018g0020a0002c0001t0018g0120others(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 | a0001c0002t0003g0205a0001c0002t0006g0197a0001c0002t0025g0199 | 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 | a0001c0002t0006g0082a0001c0002t0050g0044a0001c0003t0010g0063others(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 | a0001c0002t0002g0033a0001c0002t0006g0195a0002c0001t0002g0117others(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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0001c0002t0001g0002a0001c0002t0001g0232a0001c0002t0004g0002 | 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 | 201 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(198): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): 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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0001c0002t0013g0037a0001c0002t0013g0040a0001c0002t0013g0041others(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 | 258 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(255): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1061+134A>T | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 10/13 | chr16 | 55549536 | ||||||
chr16:55549638
|
G | A | 188 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(185): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): 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 | a0001c0002t0009g0067a0001c0002t0009g0070 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0001c0002t0016g0084a0001c0002t0036g0011 | 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 | a0002c0001t0065g0135a0002c0001t0067g0140 | 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 | a0002c0001t0003g0157 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0013g0037a0001c0002t0013g0040a0001c0002t0013g0041others(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 | 188 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(185): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0013g0037a0001c0002t0013g0040a0001c0002t0013g0041others(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 | a0003c0004t0039g0188 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0016g0084a0001c0002t0036g0011 | 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 | 252 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(249): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0008c0012t0041g0224 | 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 | a0003c0004t0022g0213a0003c0004t0039g0187a0003c0004t0039g0188others(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 | a0001c0002t0004g0260 | 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 | 188 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(185): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1215+1277G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55552379 | ||||||
chr16:55552608
|
C | T | 72 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(69): Show | 83 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(80): 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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0013g0037a0001c0002t0013g0040a0001c0002t0013g0041others(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 | 258 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(255): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): 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 | 258 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(255): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1215+1950G>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553052 | ||||||
chr16:55553056
|
A | AT | 258 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(255): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): 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 | a0001c0002t0009g0067a0001c0002t0009g0068a0001c0002t0009g0069others(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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0001c0002t0040g0235 | 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 | 204 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(201): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | 258 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(255): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1215+2188T>C | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55553290 | ||||||
chr16:55553461
|
G | A | 258 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(255): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): 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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0001c0002t0001g0237 | 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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0003c0004t0039g0188 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0001g0264a0001c0011t0001g0265 | 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0001c0003t0011g0042a0001c0003t0038g0032 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0013g0037a0001c0002t0013g0040a0001c0002t0013g0041others(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 | 188 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(185): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0014g0094others(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 | a0002c0001t0028g0147 | 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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0001c0002t0006g0082a0001c0002t0016g0081 | 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 | a0001c0002t0013g0037a0001c0002t0013g0040a0001c0002t0013g0041others(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 | a0001c0002t0007g0240 | 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 | a0001c0002t0004g0052a0001c0002t0006g0082a0001c0002t0013g0037others(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 | a0001c0002t0013g0037a0001c0002t0013g0040a0001c0002t0013g0041others(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 | a0002c0001t0003g0113a0002c0001t0003g0212 | 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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0014g0094others(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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0002c0001t0002g0136a0002c0001t0003g0166 | 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 | a0001c0002t0016g0084a0001c0002t0036g0011 | 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 | 188 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(185): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0002c0001t0006g0176 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0002c0001t0048g0167 | 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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0009g0074a0001c0002t0031g0073a0001c0002t0031g0075 | 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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0002c0001t0012g0102a0002c0001t0012g0103a0002c0001t0012g0105others(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 | a0001c0002t0001g0266a0001c0002t0001g0270 | 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 | a0004c0006t0023g0089 | 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 | a0003c0004t0022g0213a0003c0004t0039g0187a0003c0004t0039g0188others(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 | a0002c0001t0005g0085a0002c0001t0005g0151a0002c0001t0005g0154 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | 71 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0051others(68): Show | 73 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(70): 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 | a0001c0002t0001g0250a0001c0002t0007g0236a0001c0002t0009g0070others(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 | a0002c0005t0010g0021a0002c0005t0010g0175 | 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | 28 | a0001c0002t0005g0058a0001c0002t0005g0203a0002c0001t0005g0003others(25): 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 | 188 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(185): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1215+9761A>G | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 11/13 | chr16 | 55560863 | ||||||
chr16:55560899
|
T | C | 110 | a0001c0002t0001g0242a0001c0002t0001g0246a0001c0002t0002g0008others(107): 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 | a0002c0001t0008g0096a0002c0001t0008g0097a0002c0001t0013g0029others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | 191 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(188): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): 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 | a0001c0002t0001g0262a0001c0002t0001g0268a0001c0002t0004g0251others(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 | a0001c0003t0059g0079a0001c0003t0060g0078 | 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 | 197 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(194): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): 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 | a0001c0002t0050g0044a0001c0003t0034g0031a0001c0003t0034g0046others(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 | a0002c0001t0015g0171a0002c0001t0019g0141 | 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 | a0005c0007t0002g0184 | 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0006g0082a0001c0002t0014g0080a0001c0002t0016g0081others(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 | a0001c0002t0016g0084a0001c0002t0036g0011 | 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 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | 258 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(255): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): 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 | a0001c0002t0006g0082a0001c0002t0013g0037a0001c0002t0013g0040others(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 | a0001c0002t0003g0205a0001c0002t0006g0082a0001c0002t0006g0197others(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 | a0001c0003t0010g0063a0001c0003t0011g0030a0001c0003t0011g0043others(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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | a0002c0001t0019g0143a0003c0004t0022g0022a0003c0004t0022g0023others(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 | 250 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(247): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): 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 | a0001c0002t0004g0215a0001c0002t0013g0066 | 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 | a0002c0001t0002g0016a0002c0001t0003g0007a0002c0001t0003g0170others(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 | a0001c0003t0010g0063a0001c0003t0011g0030a0001c0003t0011g0043others(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 | a0002c0001t0057g0130a0003c0004t0022g0213a0003c0004t0039g0187others(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 | 81 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(78): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): 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 | a0001c0003t0010g0034a0001c0003t0071g0038 | 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 | a0003c0004t0039g0187 | 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0003c0004t0022g0022others(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 | 171 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(168): 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 | a0001c0002t0001g0254 | 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 | a0001c0002t0005g0203 | 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 | 28 | a0001c0002t0005g0058a0001c0002t0005g0203a0002c0001t0005g0003others(25): 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 | a0001c0003t0010g0034a0001c0003t0010g0036a0001c0003t0010g0063others(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 | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | a0002c0001t0014g0094a0002c0001t0014g0095 | 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 | a0002c0001t0005g0131 | 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | 262 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(259): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): 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 | a0003c0004t0077g0192 | 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 | a0004c0006t0023g0088 | 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 | a0004c0006t0023g0012a0004c0006t0023g0088a0004c0006t0023g0089others(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 | a0001c0002t0001g0267 | 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 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(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 | a0002c0001t0066g0139 | 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0003c0004t0022g0022others(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 | 166 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(163): 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 | a0002c0001t0018g0018a0002c0001t0018g0020a0002c0001t0018g0120others(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 | 262 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(259): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): 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 | a0002c0001t0003g0173a0002c0001t0016g0172a0002c0001t0058g0186 | 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 | a0002c0001t0016g0172a0002c0001t0058g0186 | 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 | a0003c0004t0039g0187 | 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 | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0003c0004t0022g0022others(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 | a0001c0002t0008g0204 | 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 | 263 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(260): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): 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 | a0002c0001t0014g0094a0002c0001t0014g0095 | 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 | a0001c0002t0001g0230 | 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 | 167 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(164): 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 | a0002c0001t0018g0018a0002c0001t0018g0020a0002c0001t0018g0120others(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 | 156 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(153): 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 | 92 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(89): Show | 103 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(100): 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 | a0002c0001t0013g0029a0002c0001t0014g0094a0002c0001t0014g0095others(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 | a0002c0001t0018g0018a0002c0001t0018g0020a0002c0001t0018g0120others(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 | a0002c0001t0016g0172 | 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 | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(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 | a0001c0002t0001g0231 | 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 | 167 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(164): 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 | a0002c0001t0056g0142 | 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0003c0004t0022g0022others(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 | a0003c0004t0077g0192 | 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 | a0002c0001t0008g0169 | 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 | a0002c0001t0058g0186 | 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 | a0003c0004t0077g0192 | 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 | a0001c0002t0035g0198 | 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 | a0001c0002t0007g0236a0001c0002t0040g0235 | 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 | a0002c0001t0033g0092a0002c0001t0033g0144 | 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 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(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 | 27 | a0001c0002t0005g0058a0001c0002t0005g0203a0002c0001t0005g0003others(24): 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 | a0002c0005t0010g0021a0002c0005t0010g0175 | 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0003c0004t0022g0022others(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 | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | 265 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(262): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): 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 | a0001c0002t0005g0203 | 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 | a0001c0002t0001g0264 | 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 | a0001c0002t0009g0074a0001c0002t0031g0073a0001c0002t0031g0075 | 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 | a0002c0001t0058g0186 | 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 | a0003c0004t0022g0213a0003c0004t0039g0187a0003c0004t0039g0188others(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 | a0001c0002t0001g0266a0001c0002t0001g0270 | 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 | 30 | a0001c0002t0005g0058a0001c0002t0005g0203a0002c0001t0005g0003others(27): 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 | 90 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(87): Show | 101 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(98): 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 | a0002c0001t0005g0133 | 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 | a0002c0001t0012g0101a0002c0001t0012g0102a0002c0001t0012g0103others(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 | a0002c0001t0002g0138 | 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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0003c0004t0022g0022others(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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | a0002c0001t0048g0167 | 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 | 262 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(259): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): 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 | a0002c0001t0008g0096a0002c0001t0008g0097 | 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 | 167 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(164): 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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0001c0002t0006g0082a0001c0002t0016g0081 | 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 | a0001c0002t0007g0257 | 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0003c0004t0022g0022others(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 | a0002c0001t0033g0144 | 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 | a0001c0002t0001g0252 | 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 | a0002c0001t0035g0164 | 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0003c0004t0022g0022others(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 | 265 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(262): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1314+617G>A | LPCAT2 | ENSG00000087253.13 | transcript | ENST00000262134.10 | protein_coding | 12/13 | chr16 | 55575346 | ||||||
chr16:55575562
|
A | G | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | 169 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(166): 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 | 84 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(81): Show | 95 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(92): 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0003c0004t0022g0022others(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 | 262 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(259): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): 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 | a0002c0001t0048g0167 | 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 | 161 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(158): 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0002c0001t0035g0164others(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 | a0002c0001t0048g0167 | 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 | a0001c0003t0010g0034a0001c0003t0010g0036a0001c0003t0010g0076others(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 | a0002c0001t0033g0092a0002c0001t0033g0144 | 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 | a0002c0001t0033g0144 | 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 | 168 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(165): 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 | a0002c0001t0005g0129 | 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 | a0001c0002t0046g0229a0002c0001t0019g0143a0003c0004t0022g0022others(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 | a0002c0001t0033g0144 | 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 | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | a0003c0004t0077g0192 | 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 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0027others(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 | a0001c0002t0046g0229a0002c0001t0019g0143a0002c0001t0032g0137others(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 | a0002c0001t0018g0018a0002c0001t0018g0020a0002c0001t0018g0120others(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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | 167 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(164): 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 | a0001c0002t0004g0215a0001c0002t0009g0067a0001c0002t0009g0068others(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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | 193 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(190): 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 | 28 | a0001c0002t0005g0058a0001c0002t0005g0203a0002c0001t0005g0003others(25): 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 | a0001c0002t0006g0197 | 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 | 200 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(197): 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 | a0002c0001t0009g0093a0002c0001t0024g0090a0002c0001t0027g0014 | 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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0002c0001t0019g0091a0006c0008t0015g0013a0006c0008t0020g0013 | 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 | a0003c0004t0077g0192 | 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 | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | a0002c0001t0048g0167 | 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 | 170 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(167): 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 | a0002c0001t0013g0029a0002c0001t0014g0094a0002c0001t0014g0095others(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 | a0001c0002t0046g0229a0003c0004t0022g0022a0003c0004t0022g0023others(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 | 28 | a0001c0002t0005g0058a0001c0002t0005g0203a0002c0001t0005g0003others(25): 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 | a0001c0003t0072g0211a0002c0001t0033g0144a0003c0004t0039g0188 | 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 |
158 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(155): 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 | 158 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(155): 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 | 158 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(155): 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 | 193 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(190): 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 | a0001c0003t0072g0211 | 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 | 175 | a0001c0002t0002g0008a0001c0002t0002g0033a0001c0002t0003g0025others(172): 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 | a0001c0002t0017g0220a0001c0002t0017g0245a0001c0002t0017g0248 | 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 | a0002c0001t0008g0169 | 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 |