geneid | 79888 |
---|---|
ensemblid | ENSG00000153395.10 |
hgncid | 25718 |
symbol | LPCAT1 |
name | lysophosphatidylcholine acyltransferase 1 |
refseq_nuc | NM_024830.5 |
refseq_prot | NP_079106.3 |
ensembl_nuc | ENST00000283415.4 |
ensembl_prot | ENSP00000283415.3 |
mane_status | MANE Select |
chr | chr5 |
start | 1461427 |
end | 1523960 |
strand | - |
ver | v1.2 |
region | chr5:1461427-1523960 |
region5000 | chr5:1456427-1528960 |
regionname0 | LPCAT1_chr5_1461427_1523960 |
regionname5000 | LPCAT1_chr5_1456427_1528960 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 534 | 328 | 83 | 54 | 146 | 11 | 32 | 105 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002 | 0/0 | 534 | 47 | 8 | 17 | 15 | 1 | 6 | 12 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0003 | 0/0 | 534 | 6 | 0 | 1 | 0 | 4 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0004 | 0/0 | 534 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0005 | 0/0 | 534 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0006 | 0/0 | 534 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0007 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
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 | 1/1 | 1605 | 126 | 31 | 27 | 49 | 5 | 12 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0002 | 0/0 | 1605 | 84 | 25 | 11 | 35 | 4 | 9 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0003 | 0/0 | 1605 | 63 | 12 | 6 | 37 | 1 | 7 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0004 | 0/0 | 1605 | 39 | 7 | 5 | 23 | 0 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0005 | 0/0 | 1605 | 36 | 4 | 14 | 13 | 1 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0006 | 0/0 | 1605 | 10 | 3 | 3 | 2 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0007 | 0/0 | 1605 | 7 | 2 | 5 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0008 | 0/0 | 1605 | 6 | 0 | 1 | 0 | 4 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0009 | 0/0 | 1605 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0010 | 0/0 | 1605 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0011 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0012 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0013 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0014 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0015 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0016 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0017 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0018 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0019 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0020 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
c0021 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
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 | 0/0 | 2341 | 90 | 26 | 8 | 45 | 3 | 8 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0002 | 0/0 | 2341 | 81 | 14 | 16 | 39 | 6 | 6 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0003 | 0/0 | 2341 | 42 | 8 | 15 | 11 | 1 | 7 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0004 | 0/1 | 2341 | 39 | 11 | 14 | 1 | 2 | 10 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0005 | 1/0 | 2341 | 33 | 6 | 5 | 21 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0006 | 0/0 | 2341 | 31 | 0 | 4 | 25 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0007 | 0/0 | 2341 | 11 | 10 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0008 | 0/0 | 2340 | 9 | 0 | 3 | 0 | 2 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0009 | 0/0 | 2342 | 7 | 7 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0010 | 0/0 | 2341 | 5 | 0 | 0 | 5 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0011 | 0/0 | 2341 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0012 | 0/0 | 2340 | 3 | 3 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0013 | 0/0 | 2341 | 3 | 0 | 0 | 2 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0014 | 0/0 | 2341 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0015 | 0/0 | 2340 | 2 | 1 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0016 | 0/0 | 2341 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0017 | 0/0 | 2327 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0018 | 0/0 | 2341 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0019 | 0/0 | 2341 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0020 | 0/0 | 2341 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0021 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0022 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0023 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0024 | 0/0 | 2341 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0025 | 0/0 | 2341 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0026 | 0/0 | 2341 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0027 | 0/0 | 2341 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0028 | 0/0 | 2341 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0029 | 0/0 | 2341 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0030 | 0/0 | 2341 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0031 | 0/0 | 2341 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0032 | 0/0 | 2341 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0033 | 0/0 | 2341 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0034 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0035 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0036 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0037 | 0/0 | 2341 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
t0038 | 0/0 | 2341 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0346 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1605 | 126 | 31 | 27 | 49 | 5 | 12 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0002 | 0/0 | 1605 | 84 | 25 | 11 | 35 | 4 | 9 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0003 | 0/0 | 1605 | 63 | 12 | 6 | 37 | 1 | 7 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0004 | 0/0 | 1605 | 39 | 7 | 5 | 23 | 0 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0007 | 0/0 | 1605 | 7 | 2 | 5 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0009 | 0/0 | 1605 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0010 | 0/0 | 1605 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0015 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0018 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0019 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0020 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0021 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0005 | 0/0 | 1605 | 36 | 4 | 14 | 13 | 1 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0006 | 0/0 | 1605 | 10 | 3 | 3 | 2 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0016 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0003c0008 | 0/0 | 1605 | 6 | 0 | 1 | 0 | 4 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0004c0012 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0004c0014 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0005c0011 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0006c0013 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0007c0017 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 3945 | 62 | 12 | 14 | 29 | 2 | 5 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0004 | 0/1 | 3945 | 22 | 5 | 8 | 0 | 1 | 7 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0005 | 1/0 | 3945 | 17 | 2 | 2 | 12 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0006 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0007 | 0/0 | 3945 | 10 | 9 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0011 | 0/0 | 3945 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0013 | 0/0 | 3945 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0018 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0019 | 0/0 | 3945 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0020 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0021 | 0/0 | 3944 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0025 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0026 | 0/0 | 3945 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0027 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0028 | 0/0 | 3945 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0029 | 0/0 | 3945 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0001t0030 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0002t0001 | 0/0 | 3945 | 54 | 17 | 6 | 25 | 2 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0002t0002 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0002t0004 | 0/0 | 3945 | 6 | 6 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0002t0006 | 0/0 | 3945 | 10 | 0 | 0 | 9 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0002t0008 | 0/0 | 3944 | 9 | 0 | 3 | 0 | 2 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0002t0015 | 0/0 | 3944 | 2 | 1 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0002t0023 | 0/0 | 3944 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0002t0036 | 0/0 | 3944 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0003t0001 | 0/0 | 3945 | 31 | 5 | 2 | 19 | 1 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0003t0006 | 0/0 | 3945 | 20 | 0 | 4 | 15 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0003t0009 | 0/0 | 3946 | 7 | 7 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0003t0014 | 0/0 | 3945 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0003t0016 | 0/0 | 3945 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0003t0033 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0004t0002 | 0/0 | 3945 | 11 | 2 | 1 | 8 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0004t0004 | 0/0 | 3945 | 4 | 0 | 1 | 0 | 0 | 3 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0004t0005 | 0/0 | 3945 | 15 | 3 | 3 | 9 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0004t0010 | 0/0 | 3945 | 4 | 0 | 0 | 4 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0004t0011 | 0/0 | 3945 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0004t0013 | 0/0 | 3945 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0004t0017 | 0/0 | 3931 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0004t0024 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0007t0004 | 0/0 | 3945 | 4 | 0 | 4 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0007t0005 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0007t0007 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0007t0022 | 0/0 | 3944 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0009t0012 | 0/0 | 3944 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0010t0001 | 0/0 | 3945 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0015t0004 | 0/0 | 3945 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0018t0010 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0019t0012 | 0/0 | 3944 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0020t0001 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0001c0021t0002 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0005t0003 | 0/0 | 3945 | 32 | 4 | 12 | 11 | 1 | 4 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0005t0004 | 0/0 | 3945 | 2 | 0 | 1 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0005t0031 | 0/0 | 3945 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0005t0037 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0006t0003 | 0/0 | 3945 | 8 | 3 | 3 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0006t0032 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0006t0038 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0002c0016t0003 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0003c0008t0002 | 0/0 | 3945 | 6 | 0 | 1 | 0 | 4 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0004c0012t0035 | 0/0 | 3944 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0004c0014t0034 | 0/0 | 3944 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0005c0011t0001 | 0/0 | 3945 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0006c0013t0003 | 0/0 | 3945 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
a0007c0017t0001 | 0/0 | 3945 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | copy fasta | chr5 | 1456427 | 1528960 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0004g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0346 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0005g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0007g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0011g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0011g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0013g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0013g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0018g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0019g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0020g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0021g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0025g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0026g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0027g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0028g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0029g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0001t0030g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0008g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0015g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0015g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0023g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0002t0036g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0009g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0014g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0014g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0016g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0016g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0003t0033g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0010g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0010g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0011g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0011g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0013g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0017g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0004t0024g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0007t0022g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0009t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0009t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0010t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0010t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0015t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0018t0010g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0019t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0020t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0001c0021t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0003g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0031g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0005t0037g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0032g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0006t0038g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0002c0016t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0003c0008t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0003c0008t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0003c0008t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0003c0008t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0003c0008t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0004c0012t0035g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0004c0014t0034g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0005c0011t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0006c0013t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
a0007c0017t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0015 | t0004 | g0254 | EUR | GBR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00099 | hp2 | a0003 | c0008 | t0002 | g0009 | EUR | GBR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00140 | hp1 | a0003 | c0008 | t0002 | g0045 | EUR | GBR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00140 | hp2 | a0001 | c0001 | t0029 | g0111 | EUR | GBR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00280 | hp1 | a0001 | c0002 | t0008 | g0128 | EUR | FIN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0223 | EUR | FIN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0360 | EUR | FIN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00323 | hp2 | a0003 | c0008 | t0002 | g0212 | EUR | FIN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0063 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0318 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00438 | hp2 | a0001 | c0004 | t0002 | g0357 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00544 | hp1 | a0002 | c0005 | t0003 | g0020 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0228 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00558 | hp1 | a0001 | c0003 | t0006 | g0180 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00597 | hp2 | a0001 | c0003 | t0033 | g0352 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00609 | hp2 | a0001 | c0004 | t0002 | g0343 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00621 | hp1 | a0001 | c0003 | t0006 | g0227 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00621 | hp2 | a0001 | c0003 | t0001 | g0338 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00639 | hp1 | a0002 | c0005 | t0031 | g0219 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0302 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00642 | hp1 | a0002 | c0005 | t0003 | g0190 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00673 | hp1 | a0002 | c0005 | t0004 | g0153 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0312 | EAS | CHS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0224 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00733 | hp2 | a0002 | c0005 | t0004 | g0146 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00735 | hp1 | a0003 | c0008 | t0002 | g0123 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0362 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01069 | hp2 | a0001 | c0004 | t0004 | g0066 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01070 | hp1 | a0002 | c0006 | t0003 | g0203 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01074 | hp2 | a0002 | c0006 | t0003 | g0102 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01081 | hp1 | a0002 | c0005 | t0003 | g0329 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01099 | hp1 | a0002 | c0005 | t0003 | g0101 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0272 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01106 | hp1 | a0001 | c0007 | t0004 | g0259 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01109 | hp1 | a0002 | c0005 | t0003 | g0186 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01109 | hp2 | a0001 | c0001 | t0026 | g0022 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01167 | hp1 | a0001 | c0003 | t0006 | g0233 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01167 | hp2 | a0002 | c0005 | t0003 | g0100 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0134 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01168 | hp2 | a0001 | c0003 | t0006 | g0007 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01175 | hp1 | a0002 | c0005 | t0003 | g0303 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01192 | hp2 | a0001 | c0004 | t0005 | g0006 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01255 | hp2 | a0001 | c0002 | t0008 | g0155 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01256 | hp1 | a0001 | c0007 | t0004 | g0257 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01256 | hp2 | a0001 | c0002 | t0008 | g0004 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01257 | hp1 | a0001 | c0007 | t0022 | g0258 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01257 | hp2 | a0001 | c0004 | t0005 | g0099 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01258 | hp1 | a0001 | c0002 | t0008 | g0004 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01258 | hp2 | a0001 | c0004 | t0005 | g0159 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01261 | hp1 | a0001 | c0004 | t0002 | g0264 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01346 | hp1 | a0001 | c0007 | t0004 | g0256 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01346 | hp2 | a0001 | c0001 | t0028 | g0350 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01358 | hp1 | a0001 | c0007 | t0004 | g0220 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01358 | hp2 | a0001 | c0002 | t0036 | g0367 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0301 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0148 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01433 | hp1 | a0002 | c0005 | t0003 | g0079 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0168 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0283 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01496 | hp2 | a0002 | c0005 | t0003 | g0108 | AMR | CLM | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01515 | hp1 | a0001 | c0002 | t0008 | g0112 | EUR | IBS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0241 | EUR | IBS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01516 | hp1 | a0003 | c0008 | t0002 | g0009 | EUR | IBS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0075 | EUR | IBS | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01884 | hp1 | a0001 | c0004 | t0002 | g0246 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01884 | hp2 | a0001 | c0001 | t0021 | g0248 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01891 | hp1 | a0002 | c0005 | t0003 | g0149 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01928 | hp2 | a0002 | c0005 | t0003 | g0213 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0173 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01943 | hp2 | a0002 | c0005 | t0003 | g0299 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01952 | hp1 | a0001 | c0003 | t0006 | g0157 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01975 | hp1 | a0002 | c0005 | t0003 | g0047 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01975 | hp2 | a0001 | c0002 | t0015 | g0298 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01978 | hp2 | a0002 | c0005 | t0003 | g0188 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01981 | hp1 | a0002 | c0006 | t0003 | g0201 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0310 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02004 | hp1 | a0001 | c0003 | t0006 | g0007 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | PEL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0359 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02015 | hp2 | a0001 | c0004 | t0005 | g0221 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02040 | hp2 | a0001 | c0003 | t0006 | g0172 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02055 | hp1 | a0002 | c0016 | t0003 | g0147 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02056 | hp2 | a0001 | c0001 | t0018 | g0018 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02083 | hp1 | a0001 | c0001 | t0005 | g0358 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02083 | hp2 | a0002 | c0005 | t0003 | g0243 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0327 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02132 | hp1 | a0001 | c0002 | t0006 | g0054 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02135 | hp1 | a0001 | c0004 | t0005 | g0006 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02135 | hp2 | a0001 | c0021 | t0002 | g0366 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02145 | hp2 | a0001 | c0004 | t0017 | g0015 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | CDX | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02155 | hp2 | a0001 | c0004 | t0002 | g0115 | EAS | CDX | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0336 | EAS | CDX | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0344 | EAS | CDX | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0349 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02258 | hp2 | a0002 | c0005 | t0003 | g0332 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02451 | hp1 | a0001 | c0019 | t0012 | g0280 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0281 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02523 | hp1 | a0001 | c0003 | t0001 | g0345 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0137 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0130 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02602 | hp2 | a0001 | c0002 | t0006 | g0204 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02615 | hp2 | a0001 | c0009 | t0012 | g0114 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02630 | hp2 | a0001 | c0004 | t0005 | g0029 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02647 | hp2 | a0001 | c0004 | t0002 | g0263 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0081 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02683 | hp2 | a0002 | c0005 | t0003 | g0363 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02698 | hp1 | a0002 | c0005 | t0003 | g0193 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02717 | hp2 | a0001 | c0003 | t0009 | g0239 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02723 | hp1 | a0001 | c0002 | t0004 | g0273 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02723 | hp2 | a0001 | c0002 | t0023 | g0245 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02735 | hp1 | a0001 | c0002 | t0008 | g0342 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02735 | hp2 | a0001 | c0003 | t0014 | g0017 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0206 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02738 | hp2 | a0002 | c0006 | t0003 | g0205 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02809 | hp1 | a0001 | c0009 | t0012 | g0105 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02886 | hp1 | a0001 | c0003 | t0009 | g0240 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0364 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0098 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0278 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0021 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0150 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0361 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02922 | hp2 | a0001 | c0020 | t0001 | g0267 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02965 | hp1 | a0002 | c0005 | t0003 | g0030 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02965 | hp2 | a0002 | c0006 | t0003 | g0031 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0215 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03041 | hp2 | a0004 | c0014 | t0034 | g0145 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03098 | hp1 | a0004 | c0012 | t0035 | g0282 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03098 | hp2 | a0001 | c0003 | t0009 | g0235 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03130 | hp1 | a0001 | c0007 | t0007 | g0110 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0269 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03139 | hp1 | a0002 | c0006 | t0003 | g0032 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03195 | hp1 | a0001 | c0003 | t0009 | g0039 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0265 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0268 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0276 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03239 | hp2 | a0002 | c0006 | t0003 | g0216 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03453 | hp1 | a0001 | c0003 | t0009 | g0012 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03486 | hp2 | a0002 | c0006 | t0003 | g0142 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03490 | hp2 | a0001 | c0002 | t0008 | g0333 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03516 | hp1 | a0001 | c0004 | t0024 | g0033 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ESN | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0279 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0365 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03579 | hp2 | a0001 | c0003 | t0009 | g0270 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0050 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0073 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0322 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03669 | hp2 | a0001 | c0004 | t0004 | g0210 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03688 | hp2 | a0001 | c0002 | t0008 | g0335 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03704 | hp2 | a0001 | c0004 | t0004 | g0260 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03710 | hp1 | a0002 | c0005 | t0003 | g0328 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03710 | hp2 | a0001 | c0003 | t0006 | g0177 | SAS | PJL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0078 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03834 | hp2 | a0002 | c0005 | t0003 | g0065 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03927 | hp1 | a0003 | c0008 | t0002 | g0353 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0202 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | BEB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG04204 | hp1 | a0006 | c0013 | t0003 | g0191 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG04204 | hp2 | a0001 | c0002 | t0008 | g0334 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG04228 | hp1 | a0001 | c0004 | t0013 | g0197 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG04228 | hp2 | a0001 | c0003 | t0014 | g0016 | SAS | STU | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0080 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0286 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18747 | hp1 | a0001 | c0004 | t0011 | g0170 | EAS | CHB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | CHB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18906 | hp1 | a0001 | c0002 | t0004 | g0143 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18906 | hp2 | a0001 | c0010 | t0001 | g0266 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18939 | hp2 | a0001 | c0004 | t0002 | g0306 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18942 | hp1 | a0002 | c0005 | t0003 | g0340 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18945 | hp1 | a0001 | c0002 | t0006 | g0117 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18945 | hp2 | a0002 | c0005 | t0003 | g0325 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18947 | hp1 | a0002 | c0005 | t0003 | g0116 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18949 | hp1 | a0001 | c0003 | t0006 | g0237 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18952 | hp2 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18953 | hp1 | a0001 | c0003 | t0006 | g0152 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18956 | hp1 | a0002 | c0006 | t0038 | g0370 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18956 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18963 | hp2 | a0001 | c0003 | t0006 | g0183 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18964 | hp1 | a0001 | c0001 | t0013 | g0040 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18964 | hp2 | a0001 | c0004 | t0010 | g0001 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18967 | hp2 | a0001 | c0002 | t0006 | g0169 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18970 | hp1 | a0001 | c0004 | t0010 | g0001 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18970 | hp2 | a0001 | c0003 | t0016 | g0368 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18971 | hp1 | a0001 | c0004 | t0005 | g0236 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18971 | hp2 | a0001 | c0004 | t0010 | g0001 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18972 | hp1 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18972 | hp2 | a0001 | c0001 | t0013 | g0053 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18974 | hp2 | a0001 | c0003 | t0006 | g0208 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18977 | hp1 | a0001 | c0003 | t0006 | g0181 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18977 | hp2 | a0001 | c0003 | t0006 | g0072 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18978 | hp2 | a0002 | c0005 | t0003 | g0171 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18979 | hp1 | a0002 | c0006 | t0032 | g0249 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18982 | hp1 | a0001 | c0001 | t0011 | g0339 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18982 | hp2 | a0001 | c0004 | t0005 | g0154 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18983 | hp2 | a0001 | c0004 | t0005 | g0160 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18986 | hp1 | a0001 | c0002 | t0006 | g0209 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18988 | hp1 | a0001 | c0004 | t0005 | g0103 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18988 | hp2 | a0001 | c0002 | t0006 | g0008 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18990 | hp2 | a0001 | c0018 | t0010 | g0179 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18991 | hp1 | a0001 | c0001 | t0011 | g0326 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18991 | hp2 | a0001 | c0004 | t0002 | g0175 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18993 | hp2 | a0001 | c0003 | t0006 | g0176 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18995 | hp1 | a0001 | c0003 | t0006 | g0192 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18997 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18999 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18999 | hp2 | a0001 | c0004 | t0002 | g0337 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0354 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19002 | hp2 | a0001 | c0001 | t0025 | g0059 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19003 | hp1 | a0001 | c0004 | t0002 | g0107 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19005 | hp2 | a0002 | c0005 | t0003 | g0308 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19009 | hp1 | a0001 | c0004 | t0002 | g0182 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19009 | hp2 | a0002 | c0005 | t0037 | g0371 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19010 | hp1 | a0002 | c0005 | t0003 | g0013 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19011 | hp1 | a0001 | c0003 | t0016 | g0369 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19011 | hp2 | a0001 | c0004 | t0005 | g0296 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19012 | hp1 | a0002 | c0005 | t0003 | g0118 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19012 | hp2 | a0001 | c0004 | t0005 | g0062 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19030 | hp2 | a0001 | c0010 | t0001 | g0275 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19056 | hp2 | a0001 | c0004 | t0010 | g0178 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19059 | hp1 | a0001 | c0003 | t0006 | g0207 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19059 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19070 | hp2 | a0002 | c0005 | t0003 | g0013 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19077 | hp1 | a0001 | c0002 | t0006 | g0315 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19077 | hp2 | a0001 | c0002 | t0006 | g0086 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19079 | hp1 | a0005 | c0011 | t0001 | g0131 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19079 | hp2 | a0001 | c0003 | t0006 | g0158 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19080 | hp2 | a0001 | c0003 | t0001 | g0164 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19081 | hp1 | a0001 | c0002 | t0006 | g0317 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19081 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19083 | hp1 | a0001 | c0001 | t0020 | g0307 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19083 | hp2 | a0001 | c0003 | t0006 | g0136 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19085 | hp2 | a0001 | c0004 | t0005 | g0061 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19086 | hp1 | a0002 | c0005 | t0003 | g0355 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19086 | hp2 | a0001 | c0002 | t0006 | g0008 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19088 | hp1 | a0001 | c0003 | t0006 | g0174 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19088 | hp2 | a0001 | c0004 | t0011 | g0356 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19240 | hp1 | a0001 | c0004 | t0005 | g0290 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0094 | AFR | YRI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20129 | hp1 | a0002 | c0005 | t0003 | g0048 | AFR | ASW | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20129 | hp2 | a0001 | c0002 | t0015 | g0288 | AFR | ASW | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20752 | hp1 | a0001 | c0001 | t0019 | g0070 | EUR | TSI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | TSI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0251 | EUR | TSI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20805 | hp2 | a0002 | c0005 | t0003 | g0330 | EUR | TSI | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20905 | hp1 | a0001 | c0004 | t0004 | g0211 | SAS | GIH | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0292 | SAS | GIH | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02109 | hp1 | a0001 | c0007 | t0005 | g0104 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02486 | hp1 | a0001 | c0003 | t0009 | g0012 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0261 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03471 | hp1 | a0001 | c0001 | t0027 | g0274 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0151 | AFR | MSL | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0122 | AFR | USA | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
HG06807 | hp2 | a0007 | c0017 | t0001 | g0097 | AFR | USA | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0271 | AFR | USA | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | USA | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA21309 | hp1 | a0001 | c0001 | t0030 | g0046 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
NA21309 | hp2 | a0001 | c0004 | t0005 | g0138 | AFR | LWK | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0023 | REF | REF | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0346 | REF | REF | LPCAT1_chr5_1456427_1528960 | LPCAT1 | chr5 | 1456427 | 1528960 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:1463691
|
G | A | 1 | a0004 | 2 | HG03041.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.1565C>T | p.Ser522Leu | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1681/3945 | 1565/1605 | 522/534 | chr5 | 1463691 | ||
chr5:1463751
|
G | A | 1 | a0006 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1505C>T | p.Ala502Val | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1621/3945 | 1505/1605 | 502/534 | chr5 | 1463751 | ||
chr5:1466889
|
A | G | 2 | a0002a0006 | 48 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
missense_variant&splice_region_variant | MODERATE | c.1280T>C | p.Met427Thr | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/14 | 1396/3945 | 1280/1605 | 427/534 | chr5 | 1466889 | ||
chr5:1489771
|
G | A | 1 | a0007 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.581C>T | p.Ala194Val | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/14 | 697/3945 | 581/1605 | 194/534 | chr5 | 1489771 | ||
chr5:1494820
|
T | C | 1 | a0003 | 6 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(3): Show |
missense_variant | MODERATE | c.373A>G | p.Thr125Ala | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/14 | 489/3945 | 373/1605 | 125/534 | chr5 | 1494820 | ||
chr5:1494844
|
C | T | 1 | a0005 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.349G>A | p.Val117Met | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/14 | 465/3945 | 349/1605 | 117/534 | chr5 | 1494844 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:1466794
|
G | A | 1 | a0001c0015 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1375C>T | p.Leu459Leu | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/14 | 1491/3945 | 1375/1605 | 459/534 | chr5 | 1466794 | ||
chr5:1466804
|
G | A | 6 | a0001c0002a0001c0003a0001c0010others(3): Show | 152 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(149): Show |
synonymous_variant | LOW | c.1365C>T | p.Thr455Thr | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/14 | 1481/3945 | 1365/1605 | 455/534 | chr5 | 1466804 | ||
chr5:1470826
|
C | T | 2 | a0001c0009a0001c0019 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1278G>A | p.Lys426Lys | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/14 | 1394/3945 | 1278/1605 | 426/534 | chr5 | 1470826 | ||
chr5:1477442
|
G | A | 1 | a0002c0016 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.861C>T | p.Pro287Pro | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/14 | 977/3945 | 861/1605 | 287/534 | chr5 | 1477442 | ||
chr5:1477457
|
C | T | 1 | a0004c0012 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.846G>A | p.Glu282Glu | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/14 | 962/3945 | 846/1605 | 282/534 | chr5 | 1477457 | ||
chr5:1494794
|
C | T | 7 | a0001c0003a0001c0004a0001c0018others(4): Show | 121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
synonymous_variant | LOW | c.399G>A | p.Ala133Ala | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/14 | 515/3945 | 399/1605 | 133/534 | chr5 | 1494794 | ||
chr5:1494845
|
G | C | 1 | a0001c0018 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.348C>G | p.Ala116Ala | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/14 | 464/3945 | 348/1605 | 116/534 | chr5 | 1494845 | ||
chr5:1501543
|
G | A | 1 | a0001c0019 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.196C>T | p.Leu66Leu | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/14 | 312/3945 | 196/1605 | 66/534 | chr5 | 1501543 | ||
chr5:1501580
|
G | A | 3 | a0001c0007a0001c0010a0001c0020 | 10 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(7): Show |
synonymous_variant | LOW | c.159C>T | p.Leu53Leu | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/14 | 275/3945 | 159/1605 | 53/534 | chr5 | 1501580 | ||
chr5:1523785
|
G | A | 1 | a0001c0021 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.60C>T | p.Asp20Asp | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/14 | 176/3945 | 60/1605 | 20/534 | chr5 | 1523785 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:1461453
|
C | T | 47 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(44): Show | 258 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2198G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 2198 | chr5 | 1461453 | |||||
chr5:1461819
|
G | A | 1 | a0001c0001t0027 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1832C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1832 | chr5 | 1461819 | |||||
chr5:1461868
|
C | T | 1 | a0001c0001t0026 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1783G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1783 | chr5 | 1461868 | |||||
chr5:1461949
|
T | C | 1 | a0001c0001t0025 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1702A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1702 | chr5 | 1461949 | |||||
chr5:1461983
|
A | G | 17 | a0001c0001t0006a0001c0001t0020a0001c0002t0001others(14): Show | 135 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1668T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1668 | chr5 | 1461983 | |||||
chr5:1462079
|
T | A | 1 | a0001c0001t0028 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1572A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1572 | chr5 | 1462079 | |||||
chr5:1462182
|
G | A | 1 | a0004c0012t0035 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1469C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1469 | chr5 | 1462182 | |||||
chr5:1462389
|
G | A | 1 | a0004c0014t0034 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1262C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1262 | chr5 | 1462389 | |||||
chr5:1462418
|
C | T | 1 | a0002c0005t0031 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1233G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1233 | chr5 | 1462418 | |||||
chr5:1462485
|
G | A | 1 | a0001c0003t0009 | 7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1166C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1166 | chr5 | 1462485 | |||||
chr5:1462539
|
C | A | 1 | a0004c0014t0034 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1112G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1112 | chr5 | 1462539 | |||||
chr5:1462543
|
G | A | 1 | a0004c0014t0034 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1108C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1108 | chr5 | 1462543 | |||||
chr5:1462605
|
G | A | 38 | a0001c0001t0004a0001c0001t0006a0001c0001t0026others(35): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*1046C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1046 | chr5 | 1462605 | |||||
chr5:1462612
|
A | T | 59 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(56): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*1039T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1039 | chr5 | 1462612 | |||||
chr5:1462617
|
G | C | 46 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(43): Show | 260 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*1034C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 1034 | chr5 | 1462617 | |||||
chr5:1462687
|
G | A | 3 | a0001c0002t0008a0001c0002t0023a0001c0002t0036 | 11 | HG00280.hp1 HG01255.hp2 HG01256.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*964C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 964 | chr5 | 1462687 | |||||
chr5:1462722
|
C | A | 2 | a0001c0001t0007a0001c0007t0007 | 11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*929G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 929 | chr5 | 1462722 | |||||
chr5:1462734
|
G | C | 1 | a0001c0001t0029 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*917C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 917 | chr5 | 1462734 | |||||
chr5:1462838
|
T | TA | 1 | a0001c0003t0009 | 7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*812dupT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 812 | chr5 | 1462838 | |||||
chr5:1462853
|
C | A | 2 | a0001c0004t0010a0001c0018t0010 | 5 | NA18964.hp2 NA18970.hp1 NA18971.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*798G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 798 | chr5 | 1462853 | |||||
chr5:1462898
|
C | T | 10 | a0001c0001t0007a0001c0001t0013a0001c0001t0021others(7): Show | 27 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*753G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 753 | chr5 | 1462898 | |||||
chr5:1462931
|
G | A | 1 | a0001c0001t0030 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*720C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 720 | chr5 | 1462931 | |||||
chr5:1462936
|
G | C | 8 | a0002c0005t0003a0002c0005t0031a0002c0005t0037others(5): Show | 46 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*715C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 715 | chr5 | 1462936 | |||||
chr5:1463009
|
TA | T | 10 | a0001c0001t0021a0001c0002t0008a0001c0002t0015others(7): Show | 20 | HG00280.hp1 HG01255.hp2 HG01256.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*641delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 641 | chr5 | 1463009 | |||||
chr5:1463011
|
A | T | 1 | a0001c0001t0021 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 640 | chr5 | 1463011 | |||||
chr5:1463088
|
A | T | 7 | a0001c0001t0006a0001c0001t0020a0001c0002t0006others(4): Show | 39 | HG00558.hp1 HG00621.hp1 HG01167.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*563T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 563 | chr5 | 1463088 | |||||
chr5:1463107
|
C | T | 1 | a0001c0001t0019 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*544G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 544 | chr5 | 1463107 | |||||
chr5:1463159
|
T | C | 1 | a0004c0012t0035 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*492A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 492 | chr5 | 1463159 | |||||
chr5:1463232
|
G | A | 1 | a0002c0006t0038 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 419 | chr5 | 1463232 | |||||
chr5:1463423
|
C | T | 2 | a0004c0012t0035a0004c0014t0034 | 2 | HG03041.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*228G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 228 | chr5 | 1463423 | |||||
chr5:1463432
|
C | T | 1 | a0001c0001t0018 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*219G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 219 | chr5 | 1463432 | |||||
chr5:1463474
|
T | C | 3 | a0001c0002t0008a0001c0002t0036a0001c0003t0033 | 11 | HG00280.hp1 HG00597.hp2 HG01255.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 177 | chr5 | 1463474 | |||||
chr5:1463541
|
C | T | 1 | a0004c0014t0034 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 110 | chr5 | 1463541 | |||||
chr5:1463575
|
C | A | 2 | a0001c0001t0011a0001c0004t0011 | 4 | NA18747.hp1 NA18982.hp1 NA18991.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*76G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 76 | chr5 | 1463575 | |||||
chr5:1463605
|
G | C | 2 | a0004c0012t0035a0004c0014t0034 | 2 | HG03041.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*46C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 14/14 | 46 | chr5 | 1463605 | |||||
chr5:1523876
|
G | A | 1 | a0001c0002t0036 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/14 | 32 | chr5 | 1523876 | |||||
chr5:1523881
|
C | T | 1 | a0001c0003t0014 | 2 | HG02735.hp2 HG04228.hp2 |
5_prime_UTR_variant | MODIFIER | c.-37G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/14 | 37 | chr5 | 1523881 | |||||
chr5:1523904
|
G | A | 3 | a0001c0003t0016a0002c0005t0037a0002c0006t0038 | 4 | NA18956.hp1 NA18970.hp2 NA19009.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-60C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/14 | 60 | chr5 | 1523904 | |||||
chr5:1523910
|
TGGGCGCG others(7): Show |
T | 1 | a0001c0004t0017 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80_-67delCGAGACCC others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/14 | 67 | chr5 | 1523910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:1463846
|
A | C | 1 | a0001c0004t0013g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1421-11T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1463846 | ||||||
chr5:1463913
|
C | T | 220 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(217): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1421-78G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1463913 | ||||||
chr5:1463924
|
G | A | 10 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(7): Show | 11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-89C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1463924 | ||||||
chr5:1463957
|
C | T | 2 | a0004c0012t0035g0282a0004c0014t0034g0145 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1421-122G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1463957 | ||||||
chr5:1464258
|
C | T | 1 | a0001c0001t0004g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1421-423G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464258 | ||||||
chr5:1464292
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1421-457G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464292 | ||||||
chr5:1464300
|
C | T | 3 | a0001c0009t0012g0105a0001c0009t0012g0114a0001c0019t0012g0280 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1421-465G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464300 | ||||||
chr5:1464316
|
C | A | 1 | a0001c0002t0008g0333 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1421-481G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464316 | ||||||
chr5:1464484
|
ACAAACAT | A | 10 | a0001c0002t0008g0004a0001c0002t0008g0112a0001c0002t0008g0128others(7): Show | 11 | HG00280.hp1 HG01255.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.1421-656_1421-650d others(9): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464484 | ||||||
chr5:1464553
|
T | G | 1 | a0001c0001t0021g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1421-718A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464553 | ||||||
chr5:1464643
|
GCA | G | 58 | a0001c0002t0008g0004a0001c0002t0008g0112a0001c0002t0008g0128others(55): Show | 61 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1421-810_1421-809d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464643 | ||||||
chr5:1464645
|
A | G | 1 | a0001c0001t0011g0339 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1421-810T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464645 | ||||||
chr5:1464665
|
A | G | 260 | a0001c0001t0002g0036a0001c0001t0002g0041a0001c0001t0002g0109others(257): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1421-830T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464665 | ||||||
chr5:1464667
|
G | A | 1 | a0001c0001t0004g0301 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1421-832C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464667 | ||||||
chr5:1464669
|
A | G | 1 | a0004c0012t0035g0282 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1421-834T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464669 | ||||||
chr5:1464676
|
C | T | 1 | a0001c0003t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1421-841G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464676 | ||||||
chr5:1464679
|
TAAAC | T | 3 | a0001c0009t0012g0105a0001c0009t0012g0114a0001c0019t0012g0280 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1421-848_1421-845d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464679 | ||||||
chr5:1464685
|
AAC | A | 13 | a0001c0001t0004g0078a0001c0001t0007g0003a0001c0001t0007g0034others(10): Show | 14 | HG01257.hp1 HG01496.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1421-852_1421-851d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464685 | ||||||
chr5:1464696
|
GCACA | G | 4 | a0001c0001t0004g0011a0001c0001t0004g0349a0001c0001t0004g0365others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1421-865_1421-862d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464696 | ||||||
chr5:1464705
|
C | CACA | 11 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(8): Show | 12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1421-871_1421-870i others(5): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464705 | ||||||
chr5:1464705
|
C | G | 3 | a0001c0001t0002g0229a0001c0001t0002g0311a0001c0001t0002g0351 | 3 | HG00558.hp2 HG00609.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1421-870G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464705 | ||||||
chr5:1464718
|
C | CAT | 10 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(7): Show | 11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-884_1421-883i others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464718 | ||||||
chr5:1464719
|
G | A | 1 | a0001c0001t0030g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1421-884C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464719 | ||||||
chr5:1464736
|
G | A | 6 | a0001c0003t0009g0012a0001c0003t0009g0039a0001c0003t0009g0235others(3): Show | 7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1421-901C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464736 | ||||||
chr5:1464736
|
GCAGA | G | 2 | a0001c0001t0002g0014a0001c0001t0002g0348 | 3 | NA18960.hp1 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1421-905_1421-902d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464736 | ||||||
chr5:1464739
|
GAC | G | 11 | a0001c0001t0004g0106a0001c0001t0007g0003a0001c0001t0007g0034others(8): Show | 12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1421-906_1421-905d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464739 | ||||||
chr5:1464754
|
A | C | 1 | a0004c0012t0035g0282 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1421-919T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464754 | ||||||
chr5:1464759
|
G | GCA | 12 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(9): Show | 13 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1421-926_1421-925d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464759 | ||||||
chr5:1464759
|
GCA | G | 4 | a0001c0002t0001g0286a0001c0009t0012g0105a0001c0009t0012g0114others(1): Show | 4 | HG02451.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1421-926_1421-925d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464759 | ||||||
chr5:1464760
|
C | G | 6 | a0001c0003t0009g0012a0001c0003t0009g0039a0001c0003t0009g0235others(3): Show | 7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1421-925G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464760 | ||||||
chr5:1464762
|
C | G | 3 | a0001c0009t0012g0105a0001c0009t0012g0114a0001c0019t0012g0280 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1421-927G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464762 | ||||||
chr5:1464783
|
C | CAT | 360 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(357): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1421-949_1421-948i others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464783 | ||||||
chr5:1464783
|
C | T | 9 | a0001c0003t0009g0012a0001c0003t0009g0039a0001c0003t0009g0235others(6): Show | 10 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1421-948G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464783 | ||||||
chr5:1464787
|
C | T | 2 | a0002c0005t0003g0171a0002c0005t0003g0355 | 2 | NA18978.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1421-952G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464787 | ||||||
chr5:1464817
|
G | A | 1 | a0001c0004t0005g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1421-982C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464817 | ||||||
chr5:1464833
|
C | T | 1 | a0001c0001t0005g0168 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1421-998G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464833 | ||||||
chr5:1464855
|
C | G | 225 | a0001c0001t0002g0036a0001c0001t0002g0041a0001c0001t0002g0109others(222): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1421-1020G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464855 | ||||||
chr5:1464874
|
T | C | 1 | a0001c0001t0021g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1421-1039A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464874 | ||||||
chr5:1464880
|
C | CACA | 259 | a0001c0001t0002g0036a0001c0001t0002g0041a0001c0001t0002g0109others(256): Show | 270 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1421-1046_1421-104 others(7): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464880 | ||||||
chr5:1464884
|
C | A | 3 | a0001c0002t0001g0291a0001c0003t0001g0230a0001c0003t0001g0231 | 3 | NA18955.hp1 NA18956.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1421-1049G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464884 | ||||||
chr5:1464893
|
A | G | 261 | a0001c0001t0002g0036a0001c0001t0002g0041a0001c0001t0002g0109others(258): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1421-1058T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464893 | ||||||
chr5:1464898
|
CACTA | C | 56 | a0001c0001t0002g0189a0001c0001t0006g0135a0001c0001t0013g0040others(53): Show | 57 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1421-1067_1421-106 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464898 | ||||||
chr5:1464929
|
AAAC | A | 10 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(7): Show | 11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-1097_1421-109 others(7): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464929 | ||||||
chr5:1464970
|
G | A | 1 | a0001c0001t0027g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1421-1135C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464970 | ||||||
chr5:1464977
|
T | C | 10 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(7): Show | 11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-1142A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464977 | ||||||
chr5:1464988
|
T | C | 232 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(229): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1421-1153A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1464988 | ||||||
chr5:1465000
|
A | C | 257 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(254): Show | 268 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1421-1165T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465000 | ||||||
chr5:1465007
|
GCA | G | 9 | a0001c0003t0009g0012a0001c0003t0009g0039a0001c0003t0009g0235others(6): Show | 10 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1421-1174_1421-117 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465007 | ||||||
chr5:1465009
|
ACACACAC others(49): Show |
A | 1 | a0001c0002t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1421-1230_1421-117 others(60): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465009 | ||||||
chr5:1465033
|
C | CACTA | 100 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(97): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1421-1202_1421-119 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465033 | ||||||
chr5:1465046
|
T | G | 6 | a0001c0003t0009g0012a0001c0003t0009g0039a0001c0003t0009g0235others(3): Show | 7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1421-1211A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465046 | ||||||
chr5:1465065
|
GCA | G | 57 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(54): Show | 59 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1421-1232_1421-123 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465065 | ||||||
chr5:1465066
|
C | A | 2 | a0004c0012t0035g0282a0004c0014t0034g0145 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1421-1231G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465066 | ||||||
chr5:1465068
|
C | A | 10 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(7): Show | 11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-1233G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465068 | ||||||
chr5:1465078
|
AAC | A | 173 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(170): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1421-1245_1421-124 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465078 | ||||||
chr5:1465116
|
GCACA | G | 47 | a0001c0010t0001g0266a0002c0005t0003g0013a0002c0005t0003g0020others(44): Show | 48 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1421-1285_1421-128 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465116 | ||||||
chr5:1465118
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1421-1283T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465118 | ||||||
chr5:1465125
|
C | T | 1 | a0002c0006t0032g0249 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1421-1290G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465125 | ||||||
chr5:1465189
|
G | A | 3 | a0001c0004t0013g0197a0004c0012t0035g0282a0004c0014t0034g0145 | 3 | HG03041.hp2 HG03098.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1421-1354C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465189 | ||||||
chr5:1465190
|
C | T | 10 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(7): Show | 11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421-1355G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465190 | ||||||
chr5:1465199
|
TAACTA | T | 3 | a0001c0001t0004g0011a0001c0001t0004g0349a0001c0001t0004g0365 | 4 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1421-1369_1421-136 others(9): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465199 | ||||||
chr5:1465270
|
GCACA | G | 3 | a0001c0009t0012g0105a0001c0009t0012g0114a0001c0019t0012g0280 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1421-1439_1421-143 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465270 | ||||||
chr5:1465272
|
A | G | 1 | a0001c0001t0011g0339 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1421-1437T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465272 | ||||||
chr5:1465284
|
G | A | 5 | a0002c0005t0003g0079a0002c0005t0003g0101a0002c0005t0003g0193others(2): Show | 5 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1421-1449C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465284 | ||||||
chr5:1465299
|
CAT | C | 3 | a0001c0001t0021g0248a0001c0002t0001g0250a0001c0002t0001g0324 | 3 | HG00408.hp2 HG01884.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1420+1448_1420+144 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465299 | ||||||
chr5:1465303
|
TGC | T | 10 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(7): Show | 11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1420+1444_1420+144 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465303 | ||||||
chr5:1465308
|
G | A | 2 | a0004c0012t0035g0282a0004c0014t0034g0145 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1420+1441C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465308 | ||||||
chr5:1465336
|
GTAAC | G | 37 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(34): Show | 39 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.1420+1409_1420+141 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465336 | ||||||
chr5:1465360
|
A | G | 1 | a0001c0019t0012g0280 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1420+1389T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465360 | ||||||
chr5:1465370
|
G | A | 2 | a0001c0001t0002g0082a0002c0005t0003g0047 | 2 | HG01975.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1420+1379C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465370 | ||||||
chr5:1465383
|
AAC | A | 24 | a0001c0002t0001g0027a0001c0002t0001g0035a0001c0002t0001g0037others(21): Show | 25 | HG01099.hp2 HG01106.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1420+1364_1420+136 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465383 | ||||||
chr5:1465400
|
A | T | 1 | a0001c0003t0001g0344 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1420+1349T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465400 | ||||||
chr5:1465421
|
GCA | G | 5 | a0001c0002t0001g0304a0001c0002t0004g0143a0002c0006t0038g0370others(2): Show | 5 | HG01928.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420+1326_1420+132 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465421 | ||||||
chr5:1465421
|
GCACA | G | 11 | a0001c0002t0008g0004a0001c0002t0008g0112a0001c0002t0008g0128others(8): Show | 12 | HG00280.hp1 HG00597.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1420+1324_1420+132 others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465421 | ||||||
chr5:1465454
|
A | G | 264 | a0001c0001t0002g0036a0001c0001t0002g0041a0001c0001t0002g0109others(261): Show | 275 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1420+1295T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465454 | ||||||
chr5:1465471
|
G | GCA | 246 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(243): Show | 256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1420+1276_1420+127 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465471 | ||||||
chr5:1465487
|
C | T | 2 | a0001c0001t0013g0040a0001c0001t0013g0053 | 2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1420+1262G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465487 | ||||||
chr5:1465494
|
G | A | 2 | a0001c0002t0001g0276a0001c0002t0001g0364 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1420+1255C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465494 | ||||||
chr5:1465502
|
TAAACACG others(9): Show |
T | 2 | a0001c0004t0002g0263a0001c0004t0002g0264 | 2 | HG01261.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1420+1231_1420+124 others(20): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465502 | ||||||
chr5:1465513
|
GCA | G | 23 | a0001c0001t0002g0069a0001c0001t0002g0076a0001c0001t0002g0124others(20): Show | 23 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1420+1234_1420+123 others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465513 | ||||||
chr5:1465613
|
G | A | 1 | a0002c0005t0003g0065 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1420+1136C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465613 | ||||||
chr5:1465615
|
A | G | 11 | a0001c0002t0008g0004a0001c0002t0008g0112a0001c0002t0008g0128others(8): Show | 12 | HG00280.hp1 HG00597.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1420+1134T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465615 | ||||||
chr5:1465617
|
A | G | 11 | a0001c0002t0008g0004a0001c0002t0008g0112a0001c0002t0008g0128others(8): Show | 12 | HG00280.hp1 HG00597.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1420+1132T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465617 | ||||||
chr5:1465647
|
C | G | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1420+1102G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465647 | ||||||
chr5:1465711
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1420+1038T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465711 | ||||||
chr5:1465742
|
A | G | 12 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(9): Show | 13 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1420+1007T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465742 | ||||||
chr5:1465778
|
A | AAC | 247 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(244): Show | 255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1420+969_1420+970d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465778 | ||||||
chr5:1465778
|
A | ACTAAAC | 8 | a0001c0001t0007g0003a0001c0001t0007g0095a0001c0001t0007g0137others(5): Show | 9 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1420+970_1420+971i others(8): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465778 | ||||||
chr5:1465833
|
C | T | 4 | a0001c0001t0002g0085a0001c0001t0002g0184a0001c0001t0002g0198others(1): Show | 4 | HG02132.hp2 NA18960.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420+916G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465833 | ||||||
chr5:1465868
|
GAAAC | G | 86 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(83): Show | 89 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.1420+877_1420+880d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465868 | ||||||
chr5:1465886
|
C | T | 1 | a0001c0004t0004g0066 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1420+863G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465886 | ||||||
chr5:1465889
|
AC | A | 34 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.1420+859delG | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465889 | ||||||
chr5:1465892
|
C | CGCACACA others(7): Show |
1 | a0001c0007t0005g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1420+843_1420+856d others(16): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465892 | ||||||
chr5:1465981
|
C | G | 4 | a0001c0001t0002g0238a0001c0004t0002g0115a0001c0004t0002g0357others(1): Show | 4 | HG00438.hp2 HG02135.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.1420+768G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1465981 | ||||||
chr5:1466030
|
G | A | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0026g0022 | 3 | HG01081.hp2 HG01109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1420+719C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466030 | ||||||
chr5:1466077
|
G | C | 1 | a0001c0004t0005g0103 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1420+672C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466077 | ||||||
chr5:1466114
|
C | A | 1 | a0001c0002t0001g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1420+635G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466114 | ||||||
chr5:1466238
|
T | A | 12 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(9): Show | 13 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1420+511A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466238 | ||||||
chr5:1466284
|
C | G | 252 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(249): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1420+465G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466284 | ||||||
chr5:1466371
|
G | T | 24 | a0001c0002t0001g0027a0001c0002t0001g0035a0001c0002t0001g0037others(21): Show | 25 | HG01099.hp2 HG01106.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1420+378C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466371 | ||||||
chr5:1466384
|
C | T | 2 | a0001c0001t0013g0040a0001c0001t0013g0053 | 2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1420+365G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466384 | ||||||
chr5:1466428
|
G | A | 1 | a0001c0002t0001g0052 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1420+321C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466428 | ||||||
chr5:1466440
|
C | T | 1 | a0002c0005t0003g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1420+309G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466440 | ||||||
chr5:1466534
|
C | G | 1 | a0001c0010t0001g0266 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1420+215G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466534 | ||||||
chr5:1466542
|
C | G | 2 | a0001c0004t0017g0015a0001c0004t0024g0033 | 2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1420+207G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466542 | ||||||
chr5:1466571
|
G | C | 246 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(243): Show | 255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1420+178C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466571 | ||||||
chr5:1466698
|
T | C | 243 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(240): Show | 251 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1420+51A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466698 | ||||||
chr5:1466701
|
A | C | 1 | a0001c0001t0002g0320 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1420+48T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466701 | ||||||
chr5:1466704
|
C | T | 1 | a0001c0003t0001g0084 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1420+45G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466704 | ||||||
chr5:1466721
|
G | A | 6 | a0001c0003t0009g0012a0001c0003t0009g0039a0001c0003t0009g0235others(3): Show | 7 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420+28C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 13/13 | chr5 | 1466721 | ||||||
chr5:1466979
|
C | T | 2 | a0002c0005t0003g0171a0002c0005t0003g0355 | 2 | NA18978.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1279-89G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1466979 | ||||||
chr5:1466996
|
G | A | 1 | a0002c0005t0004g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1279-106C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1466996 | ||||||
chr5:1467018
|
G | A | 1 | a0001c0003t0009g0235 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1279-128C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467018 | ||||||
chr5:1467130
|
G | A | 255 | a0001c0001t0002g0041a0001c0001t0002g0189a0001c0001t0002g0255others(252): Show | 264 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1279-240C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467130 | ||||||
chr5:1467160
|
G | A | 2 | a0004c0012t0035g0282a0004c0014t0034g0145 | 2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1279-270C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467160 | ||||||
chr5:1467236
|
C | T | 10 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(7): Show | 11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279-346G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467236 | ||||||
chr5:1467239
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1279-349G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467239 | ||||||
chr5:1467315
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1279-425G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467315 | ||||||
chr5:1467385
|
G | A | 10 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(7): Show | 11 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279-495C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467385 | ||||||
chr5:1467392
|
G | A | 3 | a0001c0009t0012g0105a0001c0009t0012g0114a0001c0019t0012g0280 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1279-502C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467392 | ||||||
chr5:1467465
|
C | T | 1 | a0002c0005t0003g0118 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1279-575G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467465 | ||||||
chr5:1467516
|
T | C | 11 | a0001c0001t0002g0087a0001c0001t0007g0003a0001c0001t0007g0034others(8): Show | 12 | HG01496.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279-626A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467516 | ||||||
chr5:1467688
|
TGCAGGGT others(57): Show |
T | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1279-862_1279-799d others(66): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467688 | ||||||
chr5:1467702
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1279-812G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467702 | ||||||
chr5:1467753
|
T | C | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1279-863A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467753 | ||||||
chr5:1467762
|
C | T | 1 | a0001c0003t0009g0239 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1279-872G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467762 | ||||||
chr5:1467797
|
G | A | 4 | a0001c0002t0004g0021a0001c0002t0004g0094a0001c0002t0004g0098others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279-907C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467797 | ||||||
chr5:1467820
|
T | G | 1 | a0001c0003t0001g0338 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1279-930A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467820 | ||||||
chr5:1467828
|
G | T | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1279-938C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467828 | ||||||
chr5:1467896
|
C | T | 143 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(140): Show | 150 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1279-1006G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467896 | ||||||
chr5:1467899
|
T | C | 3 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197 | 3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1279-1009A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467899 | ||||||
chr5:1467928
|
T | G | 1 | a0001c0002t0004g0021 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1279-1038A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1467928 | ||||||
chr5:1468008
|
T | TGGGAGGG others(16): Show |
1 | a0001c0007t0004g0256 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1279-1141_1279-111 others(27): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468008 | ||||||
chr5:1468055
|
C | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0241a0003c0008t0002g0009others(2): Show | 6 | HG00099.hp2 HG00323.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-1165G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468055 | ||||||
chr5:1468055
|
C | G | 271 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(268): Show | 281 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1279-1165G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468055 | ||||||
chr5:1468095
|
C | G | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1279-1205G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468095 | ||||||
chr5:1468098
|
C | T | 1 | a0001c0001t0021g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279-1208G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468098 | ||||||
chr5:1468129
|
G | C | 124 | a0001c0001t0004g0301a0001c0001t0005g0064a0001c0001t0005g0323others(121): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1279-1239C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468129 | ||||||
chr5:1468172
|
C | A | 162 | a0001c0001t0002g0041a0001c0001t0002g0255a0001c0001t0002g0262others(159): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1279-1282G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468172 | ||||||
chr5:1468280
|
A | G | 1 | a0001c0001t0004g0134 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1279-1390T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468280 | ||||||
chr5:1468405
|
C | G | 1 | a0001c0001t0002g0184 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1279-1515G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468405 | ||||||
chr5:1468618
|
T | C | 32 | a0001c0001t0002g0041a0001c0001t0002g0069a0001c0001t0002g0255others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.1279-1728A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468618 | ||||||
chr5:1468682
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1279-1792T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468682 | ||||||
chr5:1468728
|
C | T | 26 | a0001c0002t0001g0027a0001c0002t0001g0035a0001c0002t0001g0037others(23): Show | 27 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1279-1838G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468728 | ||||||
chr5:1468741
|
C | T | 1 | a0001c0001t0005g0316 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1279-1851G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468741 | ||||||
chr5:1468767
|
T | C | 2 | a0001c0001t0013g0040a0001c0001t0013g0053 | 2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1279-1877A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468767 | ||||||
chr5:1468802
|
G | T | 1 | a0001c0001t0021g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279-1912C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468802 | ||||||
chr5:1468874
|
C | T | 4 | a0001c0001t0002g0241a0003c0008t0002g0009a0003c0008t0002g0212others(1): Show | 5 | HG00099.hp2 HG00323.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1278+1952G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1468874 | ||||||
chr5:1469029
|
G | A | 3 | a0001c0002t0001g0253a0001c0002t0001g0277a0007c0017t0001g0097 | 3 | HG02257.hp2 HG02615.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1278+1797C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469029 | ||||||
chr5:1469055
|
G | A | 1 | a0001c0002t0023g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1278+1771C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469055 | ||||||
chr5:1469107
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1278+1719G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469107 | ||||||
chr5:1469147
|
G | C | 11 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(8): Show | 12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1278+1679C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469147 | ||||||
chr5:1469283
|
C | T | 1 | a0001c0001t0025g0059 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1278+1543G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469283 | ||||||
chr5:1469322
|
A | G | 102 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0038others(99): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1278+1504T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469322 | ||||||
chr5:1469603
|
C | G | 1 | a0001c0002t0001g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1278+1223G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469603 | ||||||
chr5:1469719
|
T | G | 1 | a0001c0001t0004g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1278+1107A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469719 | ||||||
chr5:1469746
|
A | G | 165 | a0001c0001t0002g0036a0001c0001t0002g0109a0001c0001t0002g0113others(162): Show | 172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.1278+1080T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469746 | ||||||
chr5:1469800
|
A | C | 3 | a0001c0001t0002g0141a0001c0001t0006g0135a0001c0004t0011g0170 | 3 | NA18747.hp1 NA18973.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1278+1026T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469800 | ||||||
chr5:1469845
|
C | A | 1 | a0001c0001t0002g0226 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1278+981G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469845 | ||||||
chr5:1469907
|
G | A | 1 | a0001c0003t0006g0227 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1278+919C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469907 | ||||||
chr5:1469954
|
G | C | 319 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(316): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1278+872C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469954 | ||||||
chr5:1469980
|
C | A | 1 | a0001c0001t0027g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1278+846G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1469980 | ||||||
chr5:1470000
|
G | A | 1 | a0002c0005t0003g0330 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1278+826C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470000 | ||||||
chr5:1470039
|
G | A | 1 | a0001c0001t0004g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1278+787C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470039 | ||||||
chr5:1470307
|
C | A | 11 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(8): Show | 12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1278+519G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470307 | ||||||
chr5:1470322
|
G | A | 3 | a0001c0003t0006g0072a0001c0003t0006g0177a0001c0003t0016g0368 | 3 | HG03710.hp2 NA18970.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1278+504C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470322 | ||||||
chr5:1470329
|
T | C | 1 | a0001c0004t0005g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1278+497A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470329 | ||||||
chr5:1470356
|
CCAGGAGT others(6): Show |
C | 1 | a0001c0003t0016g0369 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1278+457_1278+469d others(15): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470356 | ||||||
chr5:1470444
|
G | A | 1 | a0001c0001t0027g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1278+382C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470444 | ||||||
chr5:1470463
|
G | A | 319 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(316): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1278+363C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470463 | ||||||
chr5:1470577
|
C | T | 35 | a0001c0001t0002g0041a0001c0001t0002g0255a0001c0001t0004g0010others(32): Show | 37 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1278+249G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470577 | ||||||
chr5:1470648
|
C | G | 7 | a0001c0002t0001g0027a0001c0002t0001g0035a0001c0002t0001g0037others(4): Show | 7 | HG02055.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1278+178G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470648 | ||||||
chr5:1470721
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1278+105A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470721 | ||||||
chr5:1470774
|
G | A | 1 | a0001c0001t0027g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1278+52C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470774 | ||||||
chr5:1470785
|
G | A | 95 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0038others(92): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1278+41C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 12/13 | chr5 | 1470785 | ||||||
chr5:1470994
|
T | C | 320 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(317): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1180-70A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1470994 | ||||||
chr5:1471066
|
TGGAA | T | 4 | a0002c0005t0003g0030a0002c0006t0003g0031a0002c0006t0003g0032others(1): Show | 4 | HG02965.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-146_1180-143d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471066 | ||||||
chr5:1471078
|
C | T | 11 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(8): Show | 12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180-154G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471078 | ||||||
chr5:1471098
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1180-174C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471098 | ||||||
chr5:1471157
|
G | C | 3 | a0001c0009t0012g0105a0001c0009t0012g0114a0001c0019t0012g0280 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1180-233C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471157 | ||||||
chr5:1471190
|
C | T | 1 | a0004c0012t0035g0282 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1180-266G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471190 | ||||||
chr5:1471194
|
G | A | 34 | a0001c0001t0002g0041a0001c0001t0002g0255a0001c0001t0004g0010others(31): Show | 36 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.1180-270C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471194 | ||||||
chr5:1471236
|
C | G | 1 | a0001c0001t0007g0095 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1180-312G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471236 | ||||||
chr5:1471273
|
G | A | 316 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(313): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1180-349C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471273 | ||||||
chr5:1471643
|
G | C | 1 | a0001c0002t0001g0313 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1180-719C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471643 | ||||||
chr5:1471713
|
G | A | 1 | a0001c0003t0001g0354 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1180-789C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471713 | ||||||
chr5:1471715
|
G | C | 3 | a0001c0009t0012g0105a0001c0009t0012g0114a0001c0019t0012g0280 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1180-791C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471715 | ||||||
chr5:1471758
|
A | C | 1 | a0001c0003t0001g0206 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1180-834T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471758 | ||||||
chr5:1471766
|
TA | T | 3 | a0001c0009t0012g0105a0001c0009t0012g0114a0001c0019t0012g0280 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1180-843delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471766 | ||||||
chr5:1471804
|
A | ACTCAGGA others(55): Show |
1 | a0001c0003t0006g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1180-942_1180-881d others(64): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471804 | ||||||
chr5:1471943
|
G | A | 1 | a0002c0006t0038g0370 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1180-1019C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1471943 | ||||||
chr5:1472011
|
A | AGCAGAGA others(42): Show |
1 | a0001c0004t0010g0178 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1180-1088_1180-108 others(53): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472011 | ||||||
chr5:1472011
|
A | AGCAGAGA others(42): Show |
1 | a0001c0001t0005g0064 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1180-1088_1180-108 others(53): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472011 | ||||||
chr5:1472011
|
A | AGCAGAGA others(42): Show |
316 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(313): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1180-1088_1180-108 others(53): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472011 | ||||||
chr5:1472129
|
T | G | 11 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(8): Show | 12 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180-1205A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472129 | ||||||
chr5:1472193
|
A | C | 36 | a0001c0001t0002g0041a0001c0001t0002g0255a0001c0001t0002g0262others(33): Show | 38 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.1180-1269T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472193 | ||||||
chr5:1472196
|
C | A | 2 | a0001c0002t0001g0250a0001c0002t0001g0324 | 2 | HG00408.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1180-1272G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472196 | ||||||
chr5:1472297
|
C | T | 1 | a0001c0002t0002g0051 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1180-1373G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472297 | ||||||
chr5:1472415
|
G | T | 1 | a0001c0001t0002g0087 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1180-1491C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472415 | ||||||
chr5:1472453
|
G | A | 2 | a0001c0004t0005g0061a0001c0004t0005g0062 | 2 | NA19012.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1179+1504C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472453 | ||||||
chr5:1472462
|
GACT | G | 152 | a0001c0001t0002g0036a0001c0001t0002g0109a0001c0001t0002g0113others(149): Show | 156 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1179+1492_1179+149 others(7): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472462 | ||||||
chr5:1472584
|
A | T | 111 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(108): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1179+1373T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472584 | ||||||
chr5:1472586
|
T | C | 319 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(316): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1179+1371A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472586 | ||||||
chr5:1472657
|
A | G | 2 | a0001c0003t0001g0063a0002c0005t0003g0340 | 2 | HG00423.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1179+1300T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472657 | ||||||
chr5:1472795
|
G | T | 9 | a0001c0001t0002g0041a0001c0001t0002g0255a0001c0001t0004g0010others(6): Show | 10 | HG00099.hp1 HG01081.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1179+1162C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472795 | ||||||
chr5:1472879
|
C | G | 2 | a0001c0001t0013g0040a0001c0001t0013g0053 | 2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1179+1078G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472879 | ||||||
chr5:1472956
|
A | G | 320 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(317): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1179+1001T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472956 | ||||||
chr5:1472998
|
T | G | 175 | a0001c0001t0002g0036a0001c0001t0002g0109a0001c0001t0002g0113others(172): Show | 183 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1179+959A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1472998 | ||||||
chr5:1473035
|
GCTCCTCT | G | 37 | a0001c0001t0002g0041a0001c0001t0002g0255a0001c0001t0002g0262others(34): Show | 39 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.1179+915_1179+921d others(9): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473035 | ||||||
chr5:1473102
|
C | T | 1 | a0001c0003t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1179+855G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473102 | ||||||
chr5:1473147
|
C | T | 1 | a0001c0001t0005g0293 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1179+810G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473147 | ||||||
chr5:1473210
|
G | C | 1 | a0001c0007t0005g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1179+747C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473210 | ||||||
chr5:1473240
|
G | T | 1 | a0002c0005t0004g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1179+717C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473240 | ||||||
chr5:1473257
|
C | A | 1 | a0001c0001t0004g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1179+700G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473257 | ||||||
chr5:1473261
|
C | A | 2 | a0001c0002t0004g0143a0001c0002t0004g0273 | 2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1179+696G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473261 | ||||||
chr5:1473382
|
C | A | 1 | a0001c0003t0001g0206 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1179+575G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473382 | ||||||
chr5:1473445
|
T | C | 320 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(317): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1179+512A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473445 | ||||||
chr5:1473590
|
C | A | 1 | a0001c0001t0002g0322 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1179+367G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473590 | ||||||
chr5:1473591
|
G | A | 1 | a0001c0001t0027g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1179+366C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473591 | ||||||
chr5:1473611
|
G | A | 4 | a0001c0002t0004g0021a0001c0002t0004g0094a0001c0002t0004g0098others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+346C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473611 | ||||||
chr5:1473637
|
G | A | 1 | a0001c0002t0006g0209 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1179+320C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473637 | ||||||
chr5:1473862
|
A | G | 321 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(318): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1179+95T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473862 | ||||||
chr5:1473933
|
C | T | 2 | a0001c0002t0004g0098a0001c0002t0004g0150 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1179+24G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 11/13 | chr5 | 1473933 | ||||||
chr5:1474689
|
C | T | 1 | a0001c0004t0004g0260 | 1 | HG03704.hp2 | splice_region_variant&intron_variant | LOW | c.900-4G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1474689 | ||||||
chr5:1474747
|
C | T | 3 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197 | 3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.900-62G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1474747 | ||||||
chr5:1474951
|
TGAGAATT others(41): Show |
T | 1 | a0001c0001t0002g0297 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.900-314_900-267del others(48): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1474951 | ||||||
chr5:1474993
|
A | T | 1 | a0001c0001t0025g0059 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.900-308T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1474993 | ||||||
chr5:1475065
|
T | C | 1 | a0001c0004t0013g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.900-380A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475065 | ||||||
chr5:1475139
|
C | T | 1 | a0001c0002t0001g0074 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.900-454G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475139 | ||||||
chr5:1475148
|
C | A | 1 | a0001c0002t0001g0195 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.900-463G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475148 | ||||||
chr5:1475163
|
C | T | 3 | a0001c0001t0004g0042a0001c0001t0004g0132a0001c0001t0004g0223 | 3 | HG00280.hp2 HG00741.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.900-478G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475163 | ||||||
chr5:1475194
|
A | G | 7 | a0001c0001t0018g0018a0001c0002t0001g0055a0001c0002t0001g0067others(4): Show | 7 | HG02056.hp2 HG02155.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.900-509T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475194 | ||||||
chr5:1475321
|
C | T | 19 | a0001c0002t0001g0027a0001c0002t0001g0035a0001c0002t0001g0037others(16): Show | 19 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.900-636G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475321 | ||||||
chr5:1475520
|
C | A | 1 | a0001c0004t0005g0062 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.900-835G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475520 | ||||||
chr5:1475656
|
A | G | 1 | a0001c0004t0013g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.900-971T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475656 | ||||||
chr5:1475733
|
CCCGAGTG others(61): Show |
C | 59 | a0001c0001t0002g0041a0001c0001t0002g0125a0001c0001t0002g0241others(56): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.900-1116_900-1049d others(70): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475733 | ||||||
chr5:1475817
|
CGGCCCCG others(62): Show |
C | 2 | a0001c0001t0002g0087a0001c0001t0021g0248 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.900-1201_900-1133d others(71): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475817 | ||||||
chr5:1475844
|
G | A | 310 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(307): Show | 323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.900-1159C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475844 | ||||||
chr5:1475913
|
G | A | 1 | a0001c0001t0021g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.900-1228C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1475913 | ||||||
chr5:1476165
|
A | G | 1 | a0001c0004t0005g0154 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.899+1239T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476165 | ||||||
chr5:1476255
|
A | G | 3 | a0001c0001t0004g0011a0001c0001t0004g0349a0001c0001t0004g0365 | 4 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+1149T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476255 | ||||||
chr5:1476271
|
G | A | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.899+1133C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476271 | ||||||
chr5:1476290
|
TTGTTCAG others(7): Show |
T | 1 | a0001c0001t0027g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.899+1100_899+1113d others(16): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476290 | ||||||
chr5:1476332
|
G | A | 1 | a0001c0002t0001g0289 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.899+1072C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476332 | ||||||
chr5:1476460
|
C | T | 1 | a0001c0002t0001g0314 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.899+944G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476460 | ||||||
chr5:1476592
|
C | G | 73 | a0001c0001t0002g0041a0001c0001t0002g0076a0001c0001t0002g0085others(70): Show | 74 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.899+812G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476592 | ||||||
chr5:1476670
|
C | A | 68 | a0001c0001t0002g0028a0001c0001t0002g0038a0001c0001t0002g0041others(65): Show | 72 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.899+734G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476670 | ||||||
chr5:1476763
|
G | C | 1 | a0002c0005t0003g0213 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.899+641C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476763 | ||||||
chr5:1476804
|
TGGGGAGG others(33): Show |
T | 4 | a0001c0001t0004g0011a0001c0001t0004g0349a0001c0001t0004g0365others(1): Show | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.899+560_899+599del others(40): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476804 | ||||||
chr5:1476844
|
G | C | 4 | a0002c0005t0003g0020a0002c0005t0003g0118a0002c0005t0003g0243others(1): Show | 4 | HG00544.hp1 HG02083.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.899+560C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476844 | ||||||
chr5:1476956
|
C | T | 1 | a0004c0012t0035g0282 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.899+448G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1476956 | ||||||
chr5:1477068
|
G | A | 3 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197 | 3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.899+336C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477068 | ||||||
chr5:1477073
|
C | A | 3 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197 | 3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.899+331G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477073 | ||||||
chr5:1477074
|
G | A | 1 | a0001c0001t0027g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.899+330C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477074 | ||||||
chr5:1477109
|
C | T | 4 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197others(1): Show | 4 | HG03098.hp1 HG04228.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.899+295G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477109 | ||||||
chr5:1477116
|
A | C | 29 | a0001c0001t0002g0041a0001c0001t0002g0255a0001c0001t0002g0262others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.899+288T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477116 | ||||||
chr5:1477195
|
C | A | 317 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(314): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.899+209G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477195 | ||||||
chr5:1477233
|
A | G | 1 | a0003c0008t0002g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.899+171T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477233 | ||||||
chr5:1477259
|
C | T | 1 | a0002c0016t0003g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.899+145G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477259 | ||||||
chr5:1477260
|
G | A | 3 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197 | 3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.899+144C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477260 | ||||||
chr5:1477262
|
TTCACCAA others(34): Show |
T | 3 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197 | 3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.899+101_899+141del others(41): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477262 | ||||||
chr5:1477290
|
G | A | 1 | a0001c0021t0002g0366 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.899+114C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 9/13 | chr5 | 1477290 | ||||||
chr5:1477524
|
G | A | 2 | a0001c0002t0004g0143a0001c0002t0004g0273 | 2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.817-38C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477524 | ||||||
chr5:1477530
|
C | G | 1 | a0001c0001t0002g0362 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.817-44G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477530 | ||||||
chr5:1477567
|
C | A | 1 | a0004c0012t0035g0282 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.817-81G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477567 | ||||||
chr5:1477598
|
T | C | 3 | a0001c0004t0017g0015a0001c0004t0024g0033a0004c0012t0035g0282 | 3 | HG02145.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.817-112A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477598 | ||||||
chr5:1477691
|
C | G | 1 | a0002c0005t0031g0219 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.817-205G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477691 | ||||||
chr5:1477700
|
T | C | 17 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(14): Show | 18 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.817-214A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477700 | ||||||
chr5:1477717
|
A | ACCTGCTG others(61): Show |
1 | a0001c0004t0010g0178 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.817-299_817-232dup others(68): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477717 | ||||||
chr5:1477717
|
ACCTGCTG others(61): Show |
A | 14 | a0001c0001t0004g0077a0001c0001t0007g0003a0001c0001t0007g0034others(11): Show | 15 | HG01192.hp1 HG01496.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.817-299_817-232del others(68): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477717 | ||||||
chr5:1477717
|
ACCTGCTG others(129): Show |
A | 5 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0002t0004g0143others(2): Show | 5 | HG02723.hp1 HG04228.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-367_817-232del | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477717 | ||||||
chr5:1477834
|
C | T | 5 | a0001c0001t0002g0005a0001c0001t0002g0093a0001c0001t0002g0144others(2): Show | 6 | NA18947.hp2 NA18949.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-348G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477834 | ||||||
chr5:1477921
|
GCCTGCTG others(61): Show |
G | 1 | a0001c0001t0021g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.817-503_817-436del others(68): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1477921 | ||||||
chr5:1478041
|
C | T | 153 | a0001c0001t0002g0036a0001c0001t0002g0109a0001c0001t0002g0113others(150): Show | 157 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.817-555G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478041 | ||||||
chr5:1478220
|
C | G | 3 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197 | 3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.817-734G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478220 | ||||||
chr5:1478280
|
C | T | 10 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0002t0004g0143others(7): Show | 10 | HG01975.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-794G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478280 | ||||||
chr5:1478332
|
T | A | 1 | a0001c0003t0006g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.817-846A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478332 | ||||||
chr5:1478596
|
A | G | 315 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(312): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.816+1025T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478596 | ||||||
chr5:1478681
|
C | T | 1 | a0004c0012t0035g0282 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.816+940G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1478681 | ||||||
chr5:1479214
|
A | T | 1 | a0001c0002t0001g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.816+407T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479214 | ||||||
chr5:1479238
|
T | A | 2 | a0001c0002t0004g0098a0001c0002t0004g0150 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.816+383A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479238 | ||||||
chr5:1479252
|
G | A | 1 | a0002c0005t0003g0332 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.816+369C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479252 | ||||||
chr5:1479356
|
C | A | 2 | a0001c0002t0004g0143a0001c0002t0004g0273 | 2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.816+265G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479356 | ||||||
chr5:1479433
|
G | A | 5 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0002t0004g0143others(2): Show | 5 | HG02723.hp1 HG04228.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+188C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479433 | ||||||
chr5:1479563
|
G | C | 307 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(304): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.816+58C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479563 | ||||||
chr5:1479617
|
G | A | 1 | a0001c0004t0004g0260 | 1 | HG03704.hp2 | splice_region_variant&intron_variant | LOW | c.816+4C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 8/13 | chr5 | 1479617 | ||||||
chr5:1479764
|
G | A | 1 | a0004c0012t0035g0282 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.762-89C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1479764 | ||||||
chr5:1479888
|
C | T | 1 | a0001c0004t0013g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.762-213G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1479888 | ||||||
chr5:1479899
|
C | T | 7 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197others(4): Show | 7 | HG02451.hp1 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.762-224G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1479899 | ||||||
chr5:1479953
|
T | A | 25 | a0001c0001t0002g0058a0001c0001t0005g0026a0001c0001t0005g0056others(22): Show | 28 | HG00597.hp1 HG01192.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.762-278A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1479953 | ||||||
chr5:1480102
|
T | C | 1 | a0001c0001t0027g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.762-427A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480102 | ||||||
chr5:1480143
|
T | C | 3 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197 | 3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.762-468A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480143 | ||||||
chr5:1480211
|
C | A | 1 | a0001c0003t0001g0090 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.762-536G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480211 | ||||||
chr5:1480332
|
C | T | 1 | a0001c0001t0002g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.761+610G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480332 | ||||||
chr5:1480353
|
T | C | 2 | a0001c0001t0002g0028a0001c0004t0002g0246 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.761+589A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480353 | ||||||
chr5:1480356
|
A | G | 3 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197 | 3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.761+586T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480356 | ||||||
chr5:1480494
|
T | C | 5 | a0001c0003t0009g0012a0001c0003t0009g0039a0001c0003t0009g0239others(2): Show | 6 | HG02486.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+448A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480494 | ||||||
chr5:1480515
|
G | A | 107 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(104): Show | 112 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.761+427C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480515 | ||||||
chr5:1480737
|
C | T | 3 | a0001c0001t0004g0011a0001c0001t0004g0349a0001c0001t0004g0365 | 4 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.761+205G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480737 | ||||||
chr5:1480780
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.761+162G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480780 | ||||||
chr5:1480791
|
C | T | 2 | a0001c0002t0004g0143a0001c0002t0004g0273 | 2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.761+151G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480791 | ||||||
chr5:1480860
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.761+82A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480860 | ||||||
chr5:1480886
|
C | T | 1 | a0001c0004t0005g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.761+56G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 7/13 | chr5 | 1480886 | ||||||
chr5:1481020
|
CAGGGCCT others(6): Show |
C | 113 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(110): Show | 119 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.727-57_727-45delTG others(11): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481020 | ||||||
chr5:1481033
|
A | C | 87 | a0001c0001t0002g0041a0001c0001t0002g0255a0001c0001t0004g0010others(84): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.727-57T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481033 | ||||||
chr5:1481098
|
A | G | 1 | a0001c0003t0001g0090 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.727-122T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481098 | ||||||
chr5:1481100
|
G | A | 1 | a0001c0003t0001g0090 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.727-124C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481100 | ||||||
chr5:1481110
|
T | A | 1 | a0001c0003t0001g0090 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.727-134A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481110 | ||||||
chr5:1481148
|
G | A | 46 | a0001c0001t0004g0106a0001c0001t0004g0301a0001c0002t0001g0025others(43): Show | 47 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.727-172C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481148 | ||||||
chr5:1481166
|
C | G | 2 | a0001c0001t0013g0040a0001c0001t0013g0053 | 2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.727-190G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481166 | ||||||
chr5:1481224
|
A | C | 30 | a0001c0002t0001g0025a0001c0002t0001g0027a0001c0002t0001g0035others(27): Show | 30 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.727-248T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481224 | ||||||
chr5:1481295
|
A | G | 81 | a0001c0001t0002g0041a0001c0001t0002g0255a0001c0001t0004g0010others(78): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.727-319T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481295 | ||||||
chr5:1481314
|
C | A | 1 | a0001c0001t0004g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.727-338G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481314 | ||||||
chr5:1481383
|
C | T | 3 | a0001c0009t0012g0105a0001c0009t0012g0114a0001c0019t0012g0280 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.727-407G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481383 | ||||||
chr5:1481434
|
C | A | 1 | a0001c0003t0001g0090 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.727-458G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481434 | ||||||
chr5:1481453
|
C | G | 1 | a0001c0004t0002g0264 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.727-477G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481453 | ||||||
chr5:1481459
|
C | G | 1 | a0001c0001t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.727-483G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481459 | ||||||
chr5:1481555
|
C | A | 1 | a0001c0004t0004g0066 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.727-579G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481555 | ||||||
chr5:1481571
|
C | T | 3 | a0001c0009t0012g0105a0001c0009t0012g0114a0001c0019t0012g0280 | 3 | HG02451.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.727-595G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481571 | ||||||
chr5:1481697
|
T | G | 1 | a0001c0015t0004g0254 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.727-721A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481697 | ||||||
chr5:1481702
|
G | A | 1 | a0001c0001t0002g0229 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.727-726C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481702 | ||||||
chr5:1481747
|
C | A | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.727-771G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481747 | ||||||
chr5:1481767
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.727-791C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481767 | ||||||
chr5:1481826
|
C | G | 1 | a0001c0004t0004g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.727-850G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481826 | ||||||
chr5:1481877
|
C | T | 4 | a0001c0004t0002g0115a0001c0004t0002g0337a0001c0004t0002g0357others(1): Show | 4 | HG00438.hp2 HG02135.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-901G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481877 | ||||||
chr5:1481880
|
C | T | 48 | a0001c0001t0004g0106a0001c0001t0004g0301a0001c0001t0027g0274others(45): Show | 49 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.727-904G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481880 | ||||||
chr5:1481883
|
G | C | 3 | a0001c0001t0013g0040a0001c0001t0013g0053a0001c0004t0013g0197 | 3 | HG04228.hp1 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.727-907C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481883 | ||||||
chr5:1481910
|
C | T | 2 | a0001c0002t0001g0202a0002c0005t0003g0186 | 2 | HG01109.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.727-934G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1481910 | ||||||
chr5:1482047
|
C | T | 1 | a0001c0004t0013g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.727-1071G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482047 | ||||||
chr5:1482056
|
C | T | 1 | a0001c0001t0002g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.727-1080G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482056 | ||||||
chr5:1482132
|
AGTGGGCT | A | 31 | a0001c0001t0004g0106a0001c0002t0001g0025a0001c0002t0001g0027others(28): Show | 31 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.727-1163_727-1157d others(9): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482132 | ||||||
chr5:1482318
|
G | C | 5 | a0001c0001t0007g0003a0001c0001t0007g0034a0001c0001t0007g0080others(2): Show | 6 | HG01496.hp1 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.726+1110C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482318 | ||||||
chr5:1482374
|
G | A | 1 | a0001c0001t0004g0023 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.726+1054C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482374 | ||||||
chr5:1482492
|
AGGCTGGG others(13): Show |
A | 1 | a0001c0003t0001g0344 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.726+916_726+935del others(20): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482492 | ||||||
chr5:1482495
|
CTGGGG | C | 141 | a0001c0001t0002g0028a0001c0001t0002g0041a0001c0001t0002g0058others(138): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.726+928_726+932del others(5): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482495 | ||||||
chr5:1482505
|
GTGGGGTG others(121): Show |
G | 1 | a0001c0007t0004g0256 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.726+795_726+922del | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482505 | ||||||
chr5:1482507
|
GGGGTGGG others(34): Show |
G | 10 | a0001c0002t0001g0025a0001c0002t0001g0253a0001c0002t0001g0277others(7): Show | 10 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+880_726+920del others(41): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482507 | ||||||
chr5:1482527
|
G | GGGGTGGG others(65): Show |
1 | a0002c0005t0003g0303 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.726+829_726+900dup others(72): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482527 | ||||||
chr5:1482527
|
GGGGTGGG others(29): Show |
G | 1 | a0001c0002t0001g0121 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.726+865_726+900del others(36): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482527 | ||||||
chr5:1482551
|
G | C | 10 | a0001c0002t0001g0025a0001c0002t0001g0253a0001c0002t0001g0277others(7): Show | 10 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+877C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482551 | ||||||
chr5:1482563
|
A | G | 10 | a0001c0002t0001g0025a0001c0002t0001g0253a0001c0002t0001g0277others(7): Show | 10 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+865T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482563 | ||||||
chr5:1482579
|
AGGGCAGG others(69): Show |
A | 35 | a0001c0001t0002g0041a0001c0001t0002g0255a0001c0001t0004g0010others(32): Show | 37 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.726+773_726+848del others(76): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482579 | ||||||
chr5:1482655
|
T | A | 2 | a0001c0007t0004g0256a0001c0010t0001g0275 | 2 | HG01346.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.726+773A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482655 | ||||||
chr5:1482666
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.726+762C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482666 | ||||||
chr5:1482702
|
T | C | 1 | a0001c0001t0002g0076 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.726+726A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482702 | ||||||
chr5:1482716
|
C | CTGGGG | 49 | a0001c0001t0004g0106a0001c0001t0004g0301a0001c0001t0027g0274others(46): Show | 50 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.726+707_726+711dup others(5): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482716 | ||||||
chr5:1482752
|
T | C | 84 | a0001c0001t0002g0028a0001c0001t0002g0058a0001c0001t0002g0069others(81): Show | 88 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.726+676A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482752 | ||||||
chr5:1482790
|
T | C | 166 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0041others(163): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.726+638A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482790 | ||||||
chr5:1482791
|
G | A | 49 | a0001c0001t0004g0106a0001c0001t0004g0301a0001c0001t0027g0274others(46): Show | 50 | HG00280.hp1 HG01099.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.726+637C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1482791 | ||||||
chr5:1483144
|
A | C | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.726+284T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1483144 | ||||||
chr5:1483151
|
C | A | 37 | a0001c0001t0004g0106a0001c0001t0027g0274a0001c0002t0001g0025others(34): Show | 37 | HG01099.hp2 HG01106.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.726+277G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1483151 | ||||||
chr5:1483362
|
G | A | 5 | a0001c0001t0027g0274a0001c0002t0004g0021a0001c0002t0004g0098others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+66C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 6/13 | chr5 | 1483362 | ||||||
chr5:1483706
|
C | T | 1 | a0002c0016t0003g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.668-220G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483706 | ||||||
chr5:1483711
|
A | AAGGAACA others(93): Show |
1 | a0001c0003t0001g0215 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.668-226_668-225ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483711 | ||||||
chr5:1483726
|
T | C | 1 | a0001c0004t0002g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.668-240A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483726 | ||||||
chr5:1483728
|
T | G | 1 | a0001c0004t0002g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.668-242A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483728 | ||||||
chr5:1483728
|
T | TTAACATC others(93): Show |
2 | a0001c0001t0002g0087a0001c0001t0004g0042 | 2 | HG00741.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.668-243_668-242ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483728 | ||||||
chr5:1483728
|
T | TTAACATC others(193): Show |
4 | a0001c0001t0004g0024a0001c0001t0026g0022a0001c0001t0028g0350others(1): Show | 4 | HG01081.hp2 HG01109.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-243_668-242ins others(200): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483728 | ||||||
chr5:1483728
|
T | TTAACATC others(93): Show |
1 | a0001c0001t0013g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.668-243_668-242ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483728 | ||||||
chr5:1483728
|
TTAACATC others(93): Show |
T | 14 | a0001c0001t0004g0023a0001c0001t0005g0168a0001c0001t0005g0316others(11): Show | 15 | HG01106.hp1 HG01192.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.668-342_668-243del others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483728 | ||||||
chr5:1483738
|
G | A | 1 | a0001c0001t0005g0293 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.668-252C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483738 | ||||||
chr5:1483742
|
G | A | 16 | a0001c0001t0004g0010a0001c0001t0004g0078a0001c0001t0004g0132others(13): Show | 18 | HG00140.hp2 HG01069.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.668-256C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483742
|
G | AAGCTGGA others(93): Show |
2 | a0001c0001t0002g0241a0001c0001t0002g0362 | 2 | HG00741.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.668-256delCinsGGTG others(97): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483742
|
G | AAGCTGGA others(193): Show |
2 | a0001c0002t0008g0128a0001c0002t0036g0367 | 2 | HG00280.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.668-256delCinsGGTG others(197): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483742
|
G | C | 17 | a0001c0001t0002g0058a0001c0001t0004g0024a0001c0001t0004g0042others(14): Show | 19 | HG00741.hp1 HG01081.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.668-256C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483742
|
G | GAGCTGGA others(93): Show |
27 | a0001c0001t0002g0087a0001c0001t0002g0189a0001c0001t0002g0347others(24): Show | 28 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.668-356_668-257dup others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483742
|
G | GAGCTGGA others(193): Show |
2 | a0001c0003t0001g0063a0001c0003t0016g0368 | 2 | HG00423.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.668-456_668-257dup others(200): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483742
|
G | GAGCTGGA others(393): Show |
1 | a0001c0003t0006g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.668-257_668-256ins others(400): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483742
|
G | GAGCTGGA others(293): Show |
1 | a0001c0002t0001g0302 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.668-257_668-256ins others(300): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483742
|
G | GAGCTGGA others(493): Show |
1 | a0001c0001t0002g0222 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.668-257_668-256ins others(500): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483742
|
G | GAGCTGGA others(93): Show |
1 | a0001c0002t0001g0309 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.668-257_668-256ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483742
|
GAGCTGGA others(93): Show |
G | 94 | a0001c0001t0002g0014a0001c0001t0002g0036a0001c0001t0002g0069others(91): Show | 97 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.668-356_668-257del others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483742 | ||||||
chr5:1483778
|
A | ATAACATT others(93): Show |
2 | a0001c0001t0005g0026a0001c0001t0005g0265 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.668-293_668-292ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483778 | ||||||
chr5:1483778
|
A | G | 6 | a0001c0002t0001g0250a0001c0003t0006g0172a0001c0003t0006g0207others(3): Show | 6 | HG00621.hp1 HG02040.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-292T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483778 | ||||||
chr5:1483787
|
C | CGCACGAG others(93): Show |
1 | a0001c0002t0001g0232 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.668-302_668-301ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483787 | ||||||
chr5:1483803
|
C | T | 4 | a0001c0001t0002g0133a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 4 | HG00408.hp1 NA18953.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-317G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483803 | ||||||
chr5:1483826
|
C | T | 14 | a0001c0001t0002g0005a0001c0001t0002g0093a0001c0001t0002g0225others(11): Show | 15 | HG00438.hp2 HG02135.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.668-340G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483826 | ||||||
chr5:1483828
|
G | T | 14 | a0001c0001t0002g0005a0001c0001t0002g0093a0001c0001t0002g0225others(11): Show | 15 | HG00438.hp2 HG02135.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.668-342C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483828 | ||||||
chr5:1483842
|
C | A | 3 | a0001c0001t0004g0023a0001c0004t0004g0211a0001c0007t0004g0259 | 3 | HG01106.hp1 NA20905.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.668-356G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483842 | ||||||
chr5:1483878
|
A | G | 1 | a0001c0002t0001g0324 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.668-392T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483878 | ||||||
chr5:1483892
|
G | GAGCTGGA others(43): Show |
2 | a0001c0001t0002g0096a0001c0001t0002g0127 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.668-456_668-407dup others(50): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483892 | ||||||
chr5:1483928
|
G | A | 1 | a0001c0004t0013g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.668-442C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483928 | ||||||
chr5:1483936
|
G | GCGCACCA others(93): Show |
1 | a0001c0002t0004g0021 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.668-451_668-450ins others(100): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483936 | ||||||
chr5:1483995
|
C | T | 6 | a0001c0002t0001g0289a0001c0002t0004g0098a0001c0002t0004g0150others(3): Show | 6 | HG01346.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.668-509G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1483995 | ||||||
chr5:1484379
|
C | T | 127 | a0001c0001t0002g0109a0001c0001t0002g0125a0001c0001t0002g0214others(124): Show | 134 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.668-893G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484379 | ||||||
chr5:1484405
|
T | C | 26 | a0001c0001t0002g0124a0001c0001t0002g0255a0001c0001t0002g0331others(23): Show | 27 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.668-919A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484405 | ||||||
chr5:1484422
|
A | G | 1 | a0001c0003t0001g0092 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.668-936T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484422 | ||||||
chr5:1484495
|
G | A | 20 | a0001c0001t0002g0124a0001c0001t0002g0255a0001c0001t0004g0023others(17): Show | 21 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.668-1009C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484495 | ||||||
chr5:1484670
|
G | A | 2 | a0001c0001t0005g0026a0001c0001t0005g0265 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.668-1184C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484670 | ||||||
chr5:1484677
|
T | C | 17 | a0001c0001t0002g0125a0001c0001t0002g0133a0001c0001t0002g0139others(14): Show | 18 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.668-1191A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484677 | ||||||
chr5:1484692
|
G | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0127 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.668-1206C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484692 | ||||||
chr5:1484711
|
G | A | 33 | a0001c0001t0002g0069a0001c0001t0002g0162a0001c0001t0002g0163others(30): Show | 34 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.668-1225C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484711 | ||||||
chr5:1484720
|
G | A | 13 | a0001c0001t0002g0362a0001c0001t0004g0130a0001c0001t0004g0134others(10): Show | 13 | HG00140.hp2 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.668-1234C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484720 | ||||||
chr5:1484769
|
T | C | 1 | a0001c0007t0005g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.668-1283A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484769 | ||||||
chr5:1484810
|
G | A | 3 | a0001c0001t0002g0214a0001c0002t0004g0094a0002c0005t0003g0325 | 3 | HG00735.hp2 NA18945.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.668-1324C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484810 | ||||||
chr5:1484819
|
CCT | C | 4 | a0001c0002t0004g0273a0001c0003t0001g0281a0001c0004t0004g0066others(1): Show | 4 | HG01069.hp2 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-1335_668-1334d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484819 | ||||||
chr5:1484877
|
A | G | 180 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(177): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.668-1391T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484877 | ||||||
chr5:1484903
|
C | G | 1 | a0002c0005t0003g0325 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.668-1417G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484903 | ||||||
chr5:1484908
|
T | C | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.668-1422A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484908 | ||||||
chr5:1484915
|
G | C | 13 | a0001c0001t0002g0014a0001c0001t0002g0348a0001c0001t0004g0106others(10): Show | 14 | HG00408.hp2 HG02723.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.668-1429C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484915 | ||||||
chr5:1484943
|
G | A | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.668-1457C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484943 | ||||||
chr5:1484949
|
C | T | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.668-1463G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484949 | ||||||
chr5:1484992
|
G | A | 1 | a0001c0004t0005g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668-1506C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1484992 | ||||||
chr5:1485007
|
C | T | 3 | a0003c0008t0002g0009a0003c0008t0002g0212a0003c0008t0002g0353 | 4 | HG00099.hp2 HG00323.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.668-1521G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485007 | ||||||
chr5:1485010
|
A | C | 123 | a0001c0001t0002g0109a0001c0001t0005g0173a0001c0001t0005g0358others(120): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.668-1524T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485010 | ||||||
chr5:1485079
|
G | C | 2 | a0001c0001t0002g0361a0001c0004t0002g0246 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.668-1593C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485079 | ||||||
chr5:1485100
|
G | T | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.668-1614C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485100 | ||||||
chr5:1485102
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.668-1616C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485102 | ||||||
chr5:1485223
|
C | A | 1 | a0001c0003t0001g0251 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.668-1737G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485223 | ||||||
chr5:1485354
|
C | A | 2 | a0001c0001t0002g0109a0004c0014t0034g0145 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.668-1868G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485354 | ||||||
chr5:1485396
|
G | C | 2 | a0001c0004t0005g0099a0001c0004t0005g0159 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.668-1910C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485396 | ||||||
chr5:1485465
|
G | T | 2 | a0001c0001t0002g0196a0001c0001t0018g0018 | 2 | HG02056.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.668-1979C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485465 | ||||||
chr5:1485467
|
G | A | 23 | a0001c0001t0002g0087a0001c0001t0002g0361a0001c0001t0004g0073others(20): Show | 24 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.668-1981C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485467 | ||||||
chr5:1485628
|
C | T | 1 | a0001c0001t0013g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.668-2142G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485628 | ||||||
chr5:1485805
|
C | T | 3 | a0001c0003t0001g0281a0001c0004t0004g0066a0001c0004t0005g0290 | 3 | HG01069.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.668-2319G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485805 | ||||||
chr5:1485852
|
G | A | 107 | a0001c0001t0002g0319a0001c0001t0002g0320a0001c0001t0005g0200others(104): Show | 113 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.668-2366C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485852 | ||||||
chr5:1485932
|
C | T | 21 | a0001c0001t0002g0124a0001c0001t0002g0255a0001c0001t0004g0023others(18): Show | 22 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.668-2446G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485932 | ||||||
chr5:1485933
|
G | A | 1 | a0002c0005t0003g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.668-2447C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485933 | ||||||
chr5:1485960
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.667+2431G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485960 | ||||||
chr5:1485964
|
G | C | 2 | a0001c0001t0002g0361a0001c0004t0002g0246 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.667+2427C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1485964 | ||||||
chr5:1486064
|
C | T | 1 | a0001c0001t0004g0134 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.667+2327G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486064 | ||||||
chr5:1486190
|
C | T | 1 | a0001c0002t0036g0367 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.667+2201G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486190 | ||||||
chr5:1486412
|
G | T | 4 | a0001c0003t0001g0327a0001c0003t0001g0336a0001c0003t0001g0338others(1): Show | 4 | HG00597.hp2 HG00621.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+1979C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486412 | ||||||
chr5:1486428
|
C | T | 2 | a0001c0001t0002g0109a0004c0014t0034g0145 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.667+1963G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486428 | ||||||
chr5:1486493
|
C | T | 3 | a0001c0003t0001g0281a0001c0004t0004g0066a0001c0004t0005g0290 | 3 | HG01069.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.667+1898G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486493 | ||||||
chr5:1486628
|
G | C | 2 | a0001c0001t0002g0109a0004c0014t0034g0145 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.667+1763C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486628 | ||||||
chr5:1486639
|
G | A | 1 | a0001c0001t0007g0283 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.667+1752C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486639 | ||||||
chr5:1486868
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.667+1523G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486868 | ||||||
chr5:1486895
|
C | A | 1 | a0001c0003t0001g0071 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.667+1496G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486895 | ||||||
chr5:1486965
|
T | C | 1 | a0001c0001t0013g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.667+1426A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486965 | ||||||
chr5:1486995
|
G | A | 1 | a0001c0003t0009g0235 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.667+1396C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1486995 | ||||||
chr5:1487004
|
C | T | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.667+1387G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487004 | ||||||
chr5:1487037
|
T | A | 1 | a0001c0003t0001g0071 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.667+1354A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487037 | ||||||
chr5:1487046
|
C | T | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.667+1345G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487046 | ||||||
chr5:1487067
|
G | A | 21 | a0001c0001t0002g0087a0001c0001t0002g0361a0001c0001t0007g0003others(18): Show | 22 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.667+1324C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487067 | ||||||
chr5:1487155
|
T | C | 195 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(192): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.667+1236A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487155 | ||||||
chr5:1487173
|
C | T | 2 | a0001c0001t0002g0109a0004c0014t0034g0145 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.667+1218G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487173 | ||||||
chr5:1487309
|
C | T | 117 | a0001c0001t0005g0358a0001c0001t0005g0359a0001c0001t0028g0350others(114): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.667+1082G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487309 | ||||||
chr5:1487359
|
G | A | 1 | a0001c0002t0004g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.667+1032C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487359 | ||||||
chr5:1487361
|
G | T | 1 | a0001c0001t0020g0307 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.667+1030C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487361 | ||||||
chr5:1487524
|
G | A | 1 | a0001c0001t0007g0003 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.667+867C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487524 | ||||||
chr5:1487548
|
G | A | 119 | a0001c0001t0002g0109a0001c0001t0005g0358a0001c0001t0005g0359others(116): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.667+843C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487548 | ||||||
chr5:1487880
|
T | C | 13 | a0001c0001t0002g0014a0001c0001t0002g0348a0001c0001t0004g0106others(10): Show | 14 | HG00408.hp2 HG02723.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.667+511A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487880 | ||||||
chr5:1487923
|
C | T | 1 | a0002c0005t0031g0219 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.667+468G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487923 | ||||||
chr5:1487942
|
C | A | 1 | a0001c0001t0007g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.667+449G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487942 | ||||||
chr5:1487991
|
C | G | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.667+400G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1487991 | ||||||
chr5:1488032
|
C | T | 7 | a0001c0001t0002g0038a0001c0001t0002g0297a0001c0001t0002g0305others(4): Show | 7 | HG00423.hp1 NA18980.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.667+359G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1488032 | ||||||
chr5:1488035
|
G | T | 21 | a0001c0001t0002g0124a0001c0001t0002g0255a0001c0001t0004g0023others(18): Show | 22 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.667+356C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1488035 | ||||||
chr5:1488102
|
G | A | 11 | a0001c0001t0002g0014a0001c0001t0002g0348a0001c0001t0004g0106others(8): Show | 12 | HG00408.hp2 HG02723.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.667+289C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1488102 | ||||||
chr5:1488387
|
A | G | 1 | a0001c0003t0014g0016 | 1 | HG04228.hp2 | splice_region_variant&intron_variant | LOW | c.667+4T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 5/13 | chr5 | 1488387 | ||||||
chr5:1488626
|
C | T | 2 | a0001c0001t0002g0109a0004c0014t0034g0145 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.607-175G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488626 | ||||||
chr5:1488874
|
T | A | 3 | a0001c0001t0002g0041a0001c0002t0001g0292a0001c0015t0004g0254 | 3 | HG00099.hp1 NA20752.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.607-423A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488874 | ||||||
chr5:1488905
|
C | T | 5 | a0001c0001t0002g0014a0001c0001t0002g0348a0001c0002t0001g0250others(2): Show | 6 | HG00408.hp2 HG02723.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-454G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488905 | ||||||
chr5:1488928
|
G | A | 22 | a0001c0001t0002g0087a0001c0001t0002g0361a0001c0001t0004g0073others(19): Show | 23 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.607-477C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488928 | ||||||
chr5:1488958
|
G | A | 118 | a0001c0001t0002g0109a0001c0001t0005g0358a0001c0001t0005g0359others(115): Show | 125 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.607-507C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488958 | ||||||
chr5:1488974
|
T | C | 157 | a0001c0001t0002g0014a0001c0001t0002g0109a0001c0001t0002g0124others(154): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.607-523A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1488974 | ||||||
chr5:1489051
|
G | A | 1 | a0001c0004t0005g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.607-600C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489051 | ||||||
chr5:1489077
|
C | T | 1 | a0001c0002t0008g0342 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.607-626G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489077 | ||||||
chr5:1489133
|
G | A | 14 | a0001c0001t0002g0125a0001c0001t0002g0133a0001c0001t0002g0139others(11): Show | 14 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.606+613C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489133 | ||||||
chr5:1489194
|
G | A | 14 | a0001c0001t0002g0125a0001c0001t0002g0133a0001c0001t0002g0139others(11): Show | 14 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.606+552C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489194 | ||||||
chr5:1489239
|
C | T | 11 | a0001c0001t0002g0014a0001c0001t0002g0348a0001c0001t0004g0106others(8): Show | 12 | HG00408.hp2 HG02723.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.606+507G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489239 | ||||||
chr5:1489270
|
A | G | 1 | a0001c0007t0005g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.606+476T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489270 | ||||||
chr5:1489273
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.606+473C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489273 | ||||||
chr5:1489286
|
G | C | 1 | a0001c0001t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.606+460C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489286 | ||||||
chr5:1489397
|
G | A | 1 | a0001c0001t0004g0224 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.606+349C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489397 | ||||||
chr5:1489465
|
G | A | 1 | a0001c0003t0006g0072 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.606+281C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489465 | ||||||
chr5:1489591
|
A | G | 194 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(191): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.606+155T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489591 | ||||||
chr5:1489616
|
C | T | 1 | a0001c0002t0004g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.606+130G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 4/13 | chr5 | 1489616 | ||||||
chr5:1489903
|
C | T | 5 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0019g0070others(2): Show | 5 | HG01081.hp2 HG01109.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-45G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1489903 | ||||||
chr5:1489904
|
C | G | 22 | a0001c0001t0002g0124a0001c0001t0002g0214a0001c0001t0002g0255others(19): Show | 23 | HG00280.hp1 HG00735.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.494-46G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1489904 | ||||||
chr5:1489905
|
G | A | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.494-47C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1489905 | ||||||
chr5:1489956
|
G | A | 1 | a0001c0002t0004g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.494-98C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1489956 | ||||||
chr5:1490009
|
A | C | 181 | a0001c0001t0002g0087a0001c0001t0002g0109a0001c0001t0002g0124others(178): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.494-151T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490009 | ||||||
chr5:1490024
|
A | C | 6 | a0001c0001t0002g0014a0001c0001t0002g0348a0001c0001t0027g0274others(3): Show | 7 | HG00408.hp2 HG02723.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.494-166T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490024 | ||||||
chr5:1490033
|
G | A | 2 | a0001c0002t0004g0094a0001c0007t0005g0104 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.494-175C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490033 | ||||||
chr5:1490080
|
A | C | 119 | a0001c0001t0002g0109a0001c0001t0005g0173a0001c0001t0005g0358others(116): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.494-222T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490080 | ||||||
chr5:1490121
|
C | T | 1 | a0001c0010t0001g0266 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.494-263G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490121 | ||||||
chr5:1490134
|
G | A | 1 | a0001c0001t0005g0323 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.494-276C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490134 | ||||||
chr5:1490229
|
C | A | 2 | a0001c0003t0001g0206a0001c0004t0004g0260 | 2 | HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.494-371G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490229 | ||||||
chr5:1490237
|
T | G | 195 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(192): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.494-379A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490237 | ||||||
chr5:1490410
|
G | T | 2 | a0001c0007t0004g0259a0001c0007t0022g0258 | 2 | HG01106.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.494-552C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490410 | ||||||
chr5:1490418
|
T | G | 2 | a0001c0004t0017g0015a0001c0004t0024g0033 | 2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.494-560A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490418 | ||||||
chr5:1490431
|
C | T | 2 | a0001c0001t0002g0109a0004c0014t0034g0145 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.494-573G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490431 | ||||||
chr5:1490479
|
T | C | 195 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(192): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.494-621A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490479 | ||||||
chr5:1490742
|
G | A | 1 | a0001c0001t0004g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.494-884C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490742 | ||||||
chr5:1490853
|
G | T | 1 | a0001c0002t0001g0324 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.494-995C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490853 | ||||||
chr5:1490872
|
C | T | 1 | a0001c0003t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494-1014G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490872 | ||||||
chr5:1490889
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.494-1031T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490889 | ||||||
chr5:1490894
|
A | G | 69 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(66): Show | 72 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.494-1036T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1490894 | ||||||
chr5:1491099
|
G | A | 1 | a0001c0001t0028g0350 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.494-1241C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491099 | ||||||
chr5:1491123
|
T | C | 2 | a0001c0002t0004g0094a0001c0007t0005g0104 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.494-1265A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491123 | ||||||
chr5:1491214
|
G | A | 114 | a0001c0001t0005g0358a0001c0001t0005g0359a0001c0001t0028g0350others(111): Show | 121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.494-1356C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491214 | ||||||
chr5:1491220
|
G | A | 1 | a0001c0002t0001g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.494-1362C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491220 | ||||||
chr5:1491222
|
A | AAGGGAAG others(46): Show |
3 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0002t0001g0291 | 3 | NA18953.hp2 NA18955.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.494-1365_494-1364i others(55): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491222 | ||||||
chr5:1491222
|
A | AAGGGAAG others(46): Show |
44 | a0001c0001t0002g0014a0001c0001t0002g0109a0001c0001t0002g0124others(41): Show | 46 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.494-1365_494-1364i others(55): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491222 | ||||||
chr5:1491242
|
G | A | 1 | a0001c0002t0001g0049 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.494-1384C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491242 | ||||||
chr5:1491262
|
C | T | 1 | a0001c0001t0007g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.494-1404G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491262 | ||||||
chr5:1491270
|
A | C | 1 | a0001c0001t0013g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.494-1412T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491270 | ||||||
chr5:1491391
|
G | C | 1 | a0001c0003t0001g0231 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.494-1533C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491391 | ||||||
chr5:1491435
|
C | T | 1 | a0001c0003t0009g0235 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.494-1577G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491435 | ||||||
chr5:1491561
|
G | A | 3 | a0001c0003t0001g0281a0001c0004t0004g0066a0001c0004t0005g0290 | 3 | HG01069.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.494-1703C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491561 | ||||||
chr5:1491621
|
C | T | 4 | a0001c0001t0004g0106a0001c0001t0007g0271a0001c0001t0028g0350others(1): Show | 4 | HG01346.hp2 HG01361.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-1763G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491621 | ||||||
chr5:1491653
|
G | A | 2 | a0001c0001t0002g0109a0004c0014t0034g0145 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.494-1795C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491653 | ||||||
chr5:1491656
|
G | A | 6 | a0001c0001t0004g0106a0001c0001t0007g0271a0001c0002t0004g0098others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-1798C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491656 | ||||||
chr5:1491773
|
G | A | 2 | a0001c0004t0004g0210a0001c0004t0004g0211 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.494-1915C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491773 | ||||||
chr5:1491909
|
A | T | 1 | a0002c0005t0003g0100 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.494-2051T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491909 | ||||||
chr5:1491967
|
G | A | 2 | a0001c0001t0002g0222a0001c0002t0001g0302 | 2 | HG00639.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.494-2109C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491967 | ||||||
chr5:1491974
|
T | C | 2 | a0001c0002t0004g0094a0001c0007t0005g0104 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.494-2116A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1491974 | ||||||
chr5:1492001
|
G | A | 15 | a0001c0001t0002g0125a0001c0001t0002g0133a0001c0001t0002g0139others(12): Show | 15 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.494-2143C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492001 | ||||||
chr5:1492087
|
G | T | 27 | a0001c0001t0002g0014a0001c0001t0002g0109a0001c0001t0002g0124others(24): Show | 29 | HG00280.hp1 HG00408.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.494-2229C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492087 | ||||||
chr5:1492150
|
C | T | 1 | a0004c0012t0035g0282 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.494-2292G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492150 | ||||||
chr5:1492250
|
A | AGCCTGGG others(19): Show |
2 | a0001c0001t0002g0109a0004c0014t0034g0145 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.494-2418_494-2393d others(28): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492250 | ||||||
chr5:1492341
|
G | A | 21 | a0001c0001t0002g0124a0001c0001t0002g0255a0001c0001t0004g0023others(18): Show | 22 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.493+2359C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492341 | ||||||
chr5:1492364
|
G | A | 1 | a0001c0003t0006g0192 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.493+2336C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492364 | ||||||
chr5:1492444
|
A | G | 195 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(192): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.493+2256T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492444 | ||||||
chr5:1492453
|
G | A | 4 | a0001c0002t0004g0098a0001c0002t0004g0150a0001c0010t0001g0266others(1): Show | 4 | HG02895.hp1 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+2247C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492453 | ||||||
chr5:1492527
|
C | T | 121 | a0001c0001t0005g0173a0001c0001t0005g0358a0001c0001t0005g0359others(118): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.493+2173G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492527 | ||||||
chr5:1492544
|
C | CTTGT | 195 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(192): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.493+2152_493+2155d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492544 | ||||||
chr5:1492640
|
C | T | 1 | a0001c0002t0004g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.493+2060G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492640 | ||||||
chr5:1492819
|
GC | G | 5 | a0001c0001t0002g0028a0001c0001t0007g0034a0001c0001t0007g0080others(2): Show | 5 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+1880delG | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492819 | ||||||
chr5:1492826
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.493+1874G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492826 | ||||||
chr5:1492856
|
C | T | 71 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(68): Show | 74 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.493+1844G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492856 | ||||||
chr5:1492910
|
C | T | 1 | a0001c0002t0001g0232 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.493+1790G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492910 | ||||||
chr5:1492928
|
A | C | 1 | a0001c0009t0012g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.493+1772T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492928 | ||||||
chr5:1492957
|
C | T | 11 | a0001c0001t0004g0073a0001c0001t0007g0003a0001c0001t0007g0137others(8): Show | 12 | HG02055.hp2 HG02451.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.493+1743G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492957 | ||||||
chr5:1492966
|
G | C | 71 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(68): Show | 74 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.493+1734C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492966 | ||||||
chr5:1492980
|
C | T | 1 | a0001c0001t0027g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.493+1720G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492980 | ||||||
chr5:1492983
|
G | A | 1 | a0004c0012t0035g0282 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.493+1717C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1492983 | ||||||
chr5:1493062
|
G | A | 1 | a0001c0007t0005g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.493+1638C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493062 | ||||||
chr5:1493423
|
G | A | 1 | a0002c0005t0003g0363 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.493+1277C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493423 | ||||||
chr5:1493467
|
G | A | 4 | a0001c0002t0004g0098a0001c0002t0004g0150a0001c0010t0001g0266others(1): Show | 4 | HG02895.hp1 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+1233C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493467 | ||||||
chr5:1493493
|
G | A | 119 | a0001c0001t0005g0358a0001c0001t0005g0359a0001c0001t0028g0350others(116): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.493+1207C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493493 | ||||||
chr5:1493532
|
G | A | 2 | a0001c0001t0004g0106a0001c0001t0007g0271 | 2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.493+1168C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493532 | ||||||
chr5:1493538
|
C | T | 1 | a0001c0001t0021g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.493+1162G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493538 | ||||||
chr5:1493631
|
A | G | 1 | a0001c0001t0013g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.493+1069T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493631 | ||||||
chr5:1493677
|
G | A | 1 | a0001c0003t0001g0338 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.493+1023C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493677 | ||||||
chr5:1493702
|
G | C | 1 | a0001c0007t0005g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.493+998C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493702 | ||||||
chr5:1493711
|
A | G | 1 | a0001c0002t0006g0204 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.493+989T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493711 | ||||||
chr5:1493712
|
G | C | 4 | a0001c0001t0002g0005a0001c0001t0002g0093a0001c0001t0002g0225others(1): Show | 5 | NA18947.hp2 NA18949.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+988C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493712 | ||||||
chr5:1493733
|
G | A | 4 | a0001c0002t0004g0098a0001c0002t0004g0150a0001c0010t0001g0266others(1): Show | 4 | HG02895.hp1 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+967C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493733 | ||||||
chr5:1493752
|
A | G | 117 | a0001c0001t0005g0358a0001c0001t0005g0359a0001c0001t0028g0350others(114): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.493+948T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493752 | ||||||
chr5:1493753
|
G | C | 1 | a0001c0001t0004g0024 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.493+947C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493753 | ||||||
chr5:1493770
|
G | A | 1 | a0001c0004t0002g0175 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.493+930C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493770 | ||||||
chr5:1493859
|
G | A | 1 | a0001c0001t0011g0326 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.493+841C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493859 | ||||||
chr5:1493955
|
G | A | 112 | a0001c0001t0005g0358a0001c0001t0005g0359a0001c0001t0028g0350others(109): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.493+745C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1493955 | ||||||
chr5:1494123
|
T | C | 193 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(190): Show | 203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.493+577A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494123 | ||||||
chr5:1494148
|
T | TG | 192 | a0001c0001t0002g0014a0001c0001t0002g0087a0001c0001t0002g0109others(189): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.493+551dupC | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494148 | ||||||
chr5:1494156
|
G | A | 1 | a0006c0013t0003g0191 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.493+544C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494156 | ||||||
chr5:1494278
|
G | A | 1 | a0002c0005t0004g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.493+422C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494278 | ||||||
chr5:1494324
|
C | T | 292 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(289): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.493+376G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494324 | ||||||
chr5:1494394
|
G | A | 2 | a0001c0001t0013g0040a0001c0002t0004g0094 | 2 | NA18964.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.493+306C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494394 | ||||||
chr5:1494412
|
G | A | 2 | a0001c0001t0004g0106a0001c0001t0007g0271 | 2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.493+288C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494412 | ||||||
chr5:1494414
|
T | TG | 43 | a0001c0001t0002g0093a0001c0001t0002g0285a0001c0001t0002g0331others(40): Show | 44 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.493+285dupC | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494414 | ||||||
chr5:1494416
|
G | C | 14 | a0001c0001t0002g0125a0001c0001t0002g0133a0001c0001t0002g0139others(11): Show | 14 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+284C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494416 | ||||||
chr5:1494417
|
G | T | 28 | a0001c0001t0002g0014a0001c0001t0002g0109a0001c0001t0002g0124others(25): Show | 30 | HG00280.hp1 HG00408.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+283C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494417 | ||||||
chr5:1494423
|
G | T | 2 | a0001c0009t0012g0105a0001c0009t0012g0114 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.493+277C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494423 | ||||||
chr5:1494428
|
C | G | 1 | a0001c0002t0001g0321 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.493+272G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494428 | ||||||
chr5:1494649
|
C | T | 27 | a0001c0001t0002g0014a0001c0001t0002g0109a0001c0001t0002g0124others(24): Show | 29 | HG00280.hp1 HG00408.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.493+51G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 3/13 | chr5 | 1494649 | ||||||
chr5:1494923
|
G | A | 1 | a0001c0003t0001g0336 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.279-9C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1494923 | ||||||
chr5:1494950
|
T | C | 2 | a0001c0001t0027g0274a0001c0002t0004g0021 | 2 | HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.279-36A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1494950 | ||||||
chr5:1495104
|
T | C | 61 | a0001c0001t0002g0058a0001c0001t0002g0069a0001c0001t0002g0125others(58): Show | 63 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.279-190A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495104 | ||||||
chr5:1495140
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.279-226C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495140 | ||||||
chr5:1495162
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.279-248G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495162 | ||||||
chr5:1495169
|
C | T | 11 | a0001c0002t0001g0276a0001c0002t0004g0094a0001c0002t0004g0098others(8): Show | 11 | HG01069.hp2 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.279-255G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495169 | ||||||
chr5:1495181
|
T | C | 35 | a0001c0001t0002g0014a0001c0001t0002g0109a0001c0001t0002g0125others(32): Show | 36 | HG00408.hp1 HG00408.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.279-267A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495181 | ||||||
chr5:1495181
|
T | G | 1 | a0001c0001t0002g0087 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279-267A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495181 | ||||||
chr5:1495250
|
A | G | 2 | a0001c0002t0008g0004a0001c0002t0008g0112 | 3 | HG01256.hp2 HG01258.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.279-336T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495250 | ||||||
chr5:1495316
|
C | T | 1 | a0001c0004t0002g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.279-402G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495316 | ||||||
chr5:1495330
|
T | TG | 29 | a0001c0001t0002g0038a0001c0001t0002g0093a0001c0001t0002g0144others(26): Show | 29 | HG00140.hp2 HG00597.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.279-417dupC | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495330 | ||||||
chr5:1495330
|
TG | T | 198 | a0001c0001t0002g0014a0001c0001t0002g0069a0001c0001t0002g0124others(195): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.279-417delC | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495330 | ||||||
chr5:1495334
|
G | C | 140 | a0001c0001t0002g0014a0001c0001t0002g0348a0001c0001t0002g0361others(137): Show | 149 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.279-420C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495334 | ||||||
chr5:1495336
|
G | C | 2 | a0001c0004t0004g0210a0001c0004t0004g0211 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.279-422C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495336 | ||||||
chr5:1495358
|
C | T | 5 | a0001c0001t0002g0028a0001c0001t0007g0034a0001c0001t0007g0080others(2): Show | 5 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.279-444G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495358 | ||||||
chr5:1495395
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.279-481A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495395 | ||||||
chr5:1495398
|
C | T | 1 | a0001c0010t0001g0266 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.279-484G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495398 | ||||||
chr5:1495615
|
T | C | 2 | a0001c0009t0012g0105a0001c0009t0012g0114 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.279-701A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495615 | ||||||
chr5:1495648
|
A | G | 236 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(233): Show | 243 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.279-734T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495648 | ||||||
chr5:1495649
|
G | T | 3 | a0001c0003t0001g0281a0001c0004t0004g0066a0001c0004t0005g0290 | 3 | HG01069.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.279-735C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495649 | ||||||
chr5:1495654
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.279-740C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495654 | ||||||
chr5:1495663
|
G | A | 1 | a0001c0004t0002g0306 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.279-749C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495663 | ||||||
chr5:1495724
|
C | T | 123 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0038others(120): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.279-810G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495724 | ||||||
chr5:1495798
|
T | C | 3 | a0001c0001t0005g0026a0001c0001t0005g0265a0001c0007t0005g0104 | 3 | HG02109.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.279-884A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1495798 | ||||||
chr5:1496010
|
A | G | 1 | a0001c0001t0013g0053 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.279-1096T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496010 | ||||||
chr5:1496098
|
C | T | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.279-1184G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496098 | ||||||
chr5:1496234
|
G | A | 33 | a0001c0001t0002g0069a0001c0001t0002g0162a0001c0001t0002g0163others(30): Show | 34 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.279-1320C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496234 | ||||||
chr5:1496289
|
G | T | 1 | a0001c0002t0004g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279-1375C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496289 | ||||||
chr5:1496293
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.279-1379C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496293 | ||||||
chr5:1496310
|
G | A | 1 | a0001c0002t0004g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279-1396C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496310 | ||||||
chr5:1496357
|
T | C | 19 | a0001c0001t0002g0096a0001c0001t0002g0127a0001c0001t0002g0255others(16): Show | 20 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.279-1443A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496357 | ||||||
chr5:1496405
|
T | C | 4 | a0001c0001t0007g0095a0001c0001t0007g0151a0001c0002t0001g0278others(1): Show | 4 | HG02895.hp2 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.279-1491A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496405 | ||||||
chr5:1496417
|
C | CA | 41 | a0001c0001t0002g0014a0001c0001t0002g0124a0001c0001t0002g0133others(38): Show | 44 | HG00408.hp1 HG00408.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.279-1504dupT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496417 | ||||||
chr5:1496417
|
CA | C | 10 | a0001c0001t0007g0095a0001c0001t0007g0151a0001c0001t0013g0040others(7): Show | 10 | HG01884.hp1 HG02895.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.279-1504delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496417 | ||||||
chr5:1496462
|
T | C | 1 | a0001c0002t0006g0086 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.279-1548A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496462 | ||||||
chr5:1496471
|
A | T | 1 | a0001c0001t0013g0053 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.279-1557T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496471 | ||||||
chr5:1496507
|
C | T | 94 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(91): Show | 97 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.279-1593G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496507 | ||||||
chr5:1496531
|
G | A | 131 | a0001c0001t0002g0014a0001c0001t0002g0038a0001c0001t0002g0082others(128): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.279-1617C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496531 | ||||||
chr5:1496606
|
C | T | 2 | a0001c0001t0007g0003a0001c0001t0007g0137 | 3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.279-1692G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496606 | ||||||
chr5:1496609
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.279-1695G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496609 | ||||||
chr5:1496675
|
T | G | 12 | a0001c0001t0002g0038a0001c0001t0002g0133a0001c0001t0002g0139others(9): Show | 12 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.279-1761A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1496675 | ||||||
chr5:1497018
|
A | G | 4 | a0001c0001t0007g0095a0001c0002t0004g0021a0001c0004t0017g0015others(1): Show | 4 | HG02145.hp2 HG02896.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.279-2104T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497018 | ||||||
chr5:1497067
|
G | A | 1 | a0001c0001t0013g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.279-2153C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497067 | ||||||
chr5:1497144
|
T | G | 1 | a0001c0004t0005g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.279-2230A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497144 | ||||||
chr5:1497237
|
A | G | 9 | a0001c0001t0002g0255a0001c0002t0008g0004a0001c0002t0008g0112others(6): Show | 10 | HG00280.hp1 HG01255.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.279-2323T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497237 | ||||||
chr5:1497279
|
G | A | 1 | a0001c0007t0004g0220 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.279-2365C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497279 | ||||||
chr5:1497445
|
G | C | 1 | a0001c0001t0013g0053 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.279-2531C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497445 | ||||||
chr5:1497493
|
G | A | 10 | a0001c0003t0001g0084a0001c0003t0006g0172a0001c0003t0006g0180others(7): Show | 10 | HG00558.hp1 HG00621.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.279-2579C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497493 | ||||||
chr5:1497504
|
G | A | 1 | a0001c0001t0002g0351 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.279-2590C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497504 | ||||||
chr5:1497511
|
T | C | 248 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(245): Show | 256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.279-2597A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497511 | ||||||
chr5:1497578
|
C | A | 1 | a0001c0004t0005g0160 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.279-2664G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497578 | ||||||
chr5:1497579
|
G | A | 1 | a0001c0001t0028g0350 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.279-2665C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497579 | ||||||
chr5:1497851
|
C | A | 1 | a0001c0001t0013g0053 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.279-2937G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1497851 | ||||||
chr5:1498066
|
G | T | 1 | a0002c0005t0003g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.279-3152C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498066 | ||||||
chr5:1498225
|
T | A | 42 | a0001c0001t0002g0069a0001c0001t0002g0162a0001c0001t0002g0163others(39): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.278+3236A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498225 | ||||||
chr5:1498234
|
C | T | 2 | a0001c0001t0002g0036a0001c0002t0001g0037 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.278+3227G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498234 | ||||||
chr5:1498249
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.278+3212C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498249 | ||||||
chr5:1498413
|
G | A | 4 | a0001c0002t0001g0286a0001c0002t0001g0287a0001c0002t0001g0289others(1): Show | 4 | HG02258.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.278+3048C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498413 | ||||||
chr5:1498415
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.278+3046C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498415 | ||||||
chr5:1498480
|
A | G | 2 | a0001c0002t0001g0232a0002c0005t0003g0116 | 2 | NA18947.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.278+2981T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498480 | ||||||
chr5:1498511
|
G | A | 1 | a0001c0002t0023g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.278+2950C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498511 | ||||||
chr5:1498539
|
A | T | 1 | a0001c0001t0013g0053 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.278+2922T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498539 | ||||||
chr5:1498550
|
T | A | 4 | a0001c0002t0001g0304a0001c0002t0001g0310a0001c0002t0015g0298others(1): Show | 4 | HG01928.hp1 HG01943.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.278+2911A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498550 | ||||||
chr5:1498599
|
T | G | 1 | a0001c0001t0004g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.278+2862A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498599 | ||||||
chr5:1498618
|
G | A | 1 | a0001c0003t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.278+2843C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498618 | ||||||
chr5:1498651
|
CAG | C | 79 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(76): Show | 81 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.278+2808_278+2809d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498651 | ||||||
chr5:1498668
|
T | C | 12 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0019g0070others(9): Show | 12 | HG01081.hp2 HG01106.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.278+2793A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498668 | ||||||
chr5:1498679
|
A | G | 7 | a0001c0002t0001g0074a0001c0002t0001g0244a0001c0002t0001g0252others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.278+2782T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498679 | ||||||
chr5:1498744
|
A | G | 60 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0085others(57): Show | 63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.278+2717T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498744 | ||||||
chr5:1498789
|
CAT | C | 6 | a0001c0003t0001g0164a0001c0003t0001g0228a0001c0003t0001g0230others(3): Show | 6 | HG00544.hp2 HG02109.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.278+2670_278+2671d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498789 | ||||||
chr5:1498838
|
T | TACAC | 26 | a0001c0001t0002g0087a0001c0001t0002g0124a0001c0001t0002g0133others(23): Show | 26 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.278+2619_278+2622d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498838 | ||||||
chr5:1498871
|
G | A | 170 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(167): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.278+2590C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498871 | ||||||
chr5:1498877
|
C | T | 7 | a0001c0002t0001g0074a0001c0002t0001g0244a0001c0002t0001g0252others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.278+2584G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498877 | ||||||
chr5:1498895
|
A | G | 2 | a0001c0001t0004g0106a0001c0001t0007g0271 | 2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.278+2566T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498895 | ||||||
chr5:1498936
|
T | TACAC | 60 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0085others(57): Show | 63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.278+2521_278+2524d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498936 | ||||||
chr5:1498942
|
C | T | 7 | a0001c0002t0001g0074a0001c0002t0001g0244a0001c0002t0001g0252others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.278+2519G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498942 | ||||||
chr5:1498994
|
G | C | 95 | a0001c0001t0002g0069a0001c0001t0002g0087a0001c0001t0002g0113others(92): Show | 98 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.278+2467C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1498994 | ||||||
chr5:1499051
|
G | A | 1 | a0001c0002t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.278+2410C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499051 | ||||||
chr5:1499060
|
C | T | 80 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0085others(77): Show | 83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.278+2401G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499060 | ||||||
chr5:1499090
|
G | A | 1 | a0001c0001t0005g0293 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.278+2371C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499090 | ||||||
chr5:1499251
|
C | T | 79 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(76): Show | 81 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.278+2210G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499251 | ||||||
chr5:1499255
|
C | T | 89 | a0001c0001t0002g0069a0001c0001t0002g0113a0001c0001t0002g0162others(86): Show | 92 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.278+2206G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499255 | ||||||
chr5:1499351
|
C | T | 79 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(76): Show | 81 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.278+2110G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499351 | ||||||
chr5:1499352
|
G | C | 1 | a0001c0001t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.278+2109C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499352 | ||||||
chr5:1499368
|
A | T | 31 | a0001c0001t0002g0087a0001c0001t0002g0214a0001c0001t0002g0242others(28): Show | 31 | HG00735.hp2 HG01106.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.278+2093T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499368 | ||||||
chr5:1499494
|
C | G | 1 | a0001c0001t0007g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.278+1967G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499494 | ||||||
chr5:1499500
|
T | G | 1 | a0001c0001t0013g0053 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.278+1961A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499500 | ||||||
chr5:1499691
|
A | G | 167 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0069others(164): Show | 173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.278+1770T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499691 | ||||||
chr5:1499704
|
C | T | 178 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(175): Show | 183 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.278+1757G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499704 | ||||||
chr5:1499750
|
C | A | 1 | a0001c0001t0002g0320 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.278+1711G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499750 | ||||||
chr5:1499776
|
C | G | 1 | a0001c0001t0005g0019 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.278+1685G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499776 | ||||||
chr5:1499802
|
T | C | 87 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(84): Show | 89 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.278+1659A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499802 | ||||||
chr5:1499856
|
C | T | 7 | a0001c0002t0001g0074a0001c0002t0001g0244a0001c0002t0001g0252others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.278+1605G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1499856 | ||||||
chr5:1500001
|
T | A | 180 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(177): Show | 185 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.278+1460A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500001 | ||||||
chr5:1500025
|
T | A | 1 | a0001c0001t0002g0320 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.278+1436A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500025 | ||||||
chr5:1500045
|
C | T | 89 | a0001c0001t0002g0069a0001c0001t0002g0113a0001c0001t0002g0162others(86): Show | 92 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.278+1416G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500045 | ||||||
chr5:1500055
|
C | G | 43 | a0001c0001t0002g0069a0001c0001t0002g0162a0001c0001t0002g0163others(40): Show | 44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+1406G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500055 | ||||||
chr5:1500134
|
C | A | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.278+1327G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500134 | ||||||
chr5:1500169
|
A | G | 1 | a0001c0001t0004g0349 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.278+1292T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500169 | ||||||
chr5:1500198
|
TGA | T | 4 | a0001c0003t0001g0327a0001c0003t0001g0336a0001c0003t0001g0338others(1): Show | 4 | HG00597.hp2 HG00621.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1261_278+1262d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500198 | ||||||
chr5:1500240
|
G | A | 1 | a0001c0002t0023g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.278+1221C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500240 | ||||||
chr5:1500252
|
G | A | 1 | a0001c0002t0023g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.278+1209C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500252 | ||||||
chr5:1500307
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.278+1154T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500307 | ||||||
chr5:1500374
|
G | T | 86 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(83): Show | 88 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.278+1087C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500374 | ||||||
chr5:1500385
|
G | A | 1 | a0001c0004t0005g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.278+1076C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500385 | ||||||
chr5:1500554
|
G | A | 3 | a0001c0001t0007g0095a0001c0004t0017g0015a0001c0004t0024g0033 | 3 | HG02145.hp2 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.278+907C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500554 | ||||||
chr5:1500928
|
G | A | 2 | a0002c0005t0003g0363a0002c0005t0031g0219 | 2 | HG00639.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.278+533C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500928 | ||||||
chr5:1500970
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.278+491G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1500970 | ||||||
chr5:1501064
|
G | C | 60 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0085others(57): Show | 63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.278+397C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501064 | ||||||
chr5:1501167
|
T | C | 180 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(177): Show | 185 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.278+294A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501167 | ||||||
chr5:1501239
|
G | T | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.278+222C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501239 | ||||||
chr5:1501306
|
C | T | 13 | a0001c0001t0002g0124a0001c0001t0002g0133a0001c0001t0002g0139others(10): Show | 13 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.278+155G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501306 | ||||||
chr5:1501333
|
G | A | 2 | a0001c0002t0006g0204a0002c0005t0003g0193 | 2 | HG02602.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.278+128C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501333 | ||||||
chr5:1501333
|
G | C | 43 | a0001c0001t0002g0069a0001c0001t0002g0162a0001c0001t0002g0163others(40): Show | 44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.278+128C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501333 | ||||||
chr5:1501409
|
T | C | 14 | a0001c0002t0004g0098a0001c0002t0004g0150a0001c0003t0001g0088others(11): Show | 15 | HG01099.hp2 HG01261.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.278+52A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501409 | ||||||
chr5:1501420
|
A | AC | 18 | a0001c0001t0002g0125a0001c0001t0002g0133a0001c0001t0002g0139others(15): Show | 18 | HG00408.hp1 HG00738.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.278+40dupG | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501420 | ||||||
chr5:1501427
|
C | A | 89 | a0001c0001t0002g0069a0001c0001t0002g0113a0001c0001t0002g0162others(86): Show | 92 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.278+34G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 2/13 | chr5 | 1501427 | ||||||
chr5:1501675
|
T | C | 180 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(177): Show | 185 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.136-72A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501675 | ||||||
chr5:1501766
|
GAGGCTGA others(3): Show |
G | 1 | a0001c0002t0023g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-173_136-164del others(10): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501766 | ||||||
chr5:1501808
|
C | T | 43 | a0001c0001t0002g0069a0001c0001t0002g0162a0001c0001t0002g0163others(40): Show | 44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.136-205G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501808 | ||||||
chr5:1501836
|
AGCACTGA others(13): Show |
A | 1 | a0001c0004t0002g0343 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.136-253_136-234del others(20): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501836 | ||||||
chr5:1501887
|
GCACTGAC others(43): Show |
G | 1 | a0001c0001t0002g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.136-334_136-285del others(50): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501887 | ||||||
chr5:1501915
|
C | T | 43 | a0001c0001t0002g0069a0001c0001t0002g0162a0001c0001t0002g0163others(40): Show | 44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.136-312G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1501915 | ||||||
chr5:1502010
|
T | C | 2 | a0001c0003t0016g0369a0002c0006t0038g0370 | 2 | NA18956.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.136-407A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502010 | ||||||
chr5:1502087
|
A | G | 180 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(177): Show | 185 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.136-484T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502087 | ||||||
chr5:1502091
|
G | A | 1 | a0001c0002t0002g0051 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.136-488C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502091 | ||||||
chr5:1502122
|
C | A | 1 | a0002c0006t0003g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136-519G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502122 | ||||||
chr5:1502144
|
C | A | 1 | a0001c0002t0023g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-541G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502144 | ||||||
chr5:1502170
|
A | C | 60 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0085others(57): Show | 63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-567T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502170 | ||||||
chr5:1502266
|
C | G | 177 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(174): Show | 181 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.136-663G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502266 | ||||||
chr5:1502338
|
A | T | 199 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(196): Show | 204 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.136-735T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502338 | ||||||
chr5:1502343
|
A | C | 1 | a0001c0004t0002g0175 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.136-740T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502343 | ||||||
chr5:1502465
|
C | T | 6 | a0001c0001t0002g0087a0001c0001t0002g0242a0001c0001t0007g0151others(3): Show | 6 | HG02109.hp2 HG02895.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-862G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502465 | ||||||
chr5:1502469
|
G | A | 2 | a0001c0003t0016g0369a0002c0006t0038g0370 | 2 | NA18956.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.136-866C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502469 | ||||||
chr5:1502564
|
G | A | 1 | a0001c0002t0023g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-961C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502564 | ||||||
chr5:1502599
|
G | A | 1 | a0001c0003t0001g0344 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.136-996C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502599 | ||||||
chr5:1502675
|
A | G | 1 | a0001c0004t0004g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.136-1072T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502675 | ||||||
chr5:1502683
|
G | A | 1 | a0001c0001t0002g0285 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136-1080C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502683 | ||||||
chr5:1502734
|
T | C | 1 | a0001c0001t0004g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.136-1131A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502734 | ||||||
chr5:1502893
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.136-1290G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502893 | ||||||
chr5:1502931
|
C | T | 79 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0085others(76): Show | 82 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.136-1328G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1502931 | ||||||
chr5:1503090
|
C | T | 79 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0085others(76): Show | 82 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.136-1487G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503090 | ||||||
chr5:1503145
|
G | A | 4 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0141others(1): Show | 4 | NA18953.hp2 NA18955.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1542C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503145 | ||||||
chr5:1503172
|
C | A | 60 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0085others(57): Show | 63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-1569G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503172 | ||||||
chr5:1503279
|
G | A | 7 | a0001c0001t0002g0113a0001c0001t0007g0095a0001c0002t0004g0098others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-1676C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503279 | ||||||
chr5:1503336
|
GA | G | 11 | a0001c0001t0013g0053a0001c0007t0004g0220a0001c0007t0004g0256others(8): Show | 11 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-1734delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503336 | ||||||
chr5:1503418
|
C | T | 1 | a0001c0003t0001g0206 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.136-1815G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503418 | ||||||
chr5:1503441
|
G | A | 2 | a0001c0001t0002g0361a0004c0014t0034g0145 | 2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.136-1838C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503441 | ||||||
chr5:1503448
|
A | T | 81 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0041others(78): Show | 84 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.136-1845T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503448 | ||||||
chr5:1503495
|
T | C | 61 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0085others(58): Show | 64 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.136-1892A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503495 | ||||||
chr5:1503514
|
C | T | 1 | a0001c0002t0002g0051 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.136-1911G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503514 | ||||||
chr5:1503541
|
T | C | 1 | a0001c0002t0008g0342 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.136-1938A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503541 | ||||||
chr5:1503652
|
C | G | 1 | a0002c0005t0031g0219 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.136-2049G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503652 | ||||||
chr5:1503696
|
G | A | 1 | a0001c0002t0001g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.136-2093C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503696 | ||||||
chr5:1503800
|
A | AT | 89 | a0001c0001t0002g0069a0001c0001t0002g0113a0001c0001t0002g0162others(86): Show | 92 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.136-2198dupA | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503800 | ||||||
chr5:1503815
|
G | A | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.136-2212C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503815 | ||||||
chr5:1503864
|
C | T | 1 | a0001c0004t0011g0356 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.136-2261G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503864 | ||||||
chr5:1503981
|
T | G | 1 | a0001c0002t0001g0234 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.136-2378A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1503981 | ||||||
chr5:1504020
|
T | C | 1 | a0001c0002t0008g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.136-2417A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504020 | ||||||
chr5:1504116
|
C | T | 56 | a0001c0001t0002g0005a0001c0001t0002g0093a0001c0001t0002g0125others(53): Show | 58 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.136-2513G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504116 | ||||||
chr5:1504310
|
G | GCGCAGCG others(8): Show |
1 | a0001c0002t0004g0273 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.136-2722_136-2708d others(17): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504310 | ||||||
chr5:1504312
|
G | A | 1 | a0001c0002t0023g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-2709C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504312 | ||||||
chr5:1504347
|
A | G | 78 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0087others(75): Show | 81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.136-2744T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504347 | ||||||
chr5:1504357
|
G | A | 10 | a0001c0007t0004g0220a0001c0007t0004g0256a0001c0007t0004g0257others(7): Show | 10 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-2754C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504357 | ||||||
chr5:1504418
|
G | C | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-2815C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504418 | ||||||
chr5:1504427
|
G | A | 1 | a0002c0006t0003g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136-2824C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504427 | ||||||
chr5:1504488
|
G | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0262 | 2 | HG00735.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.136-2885C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504488 | ||||||
chr5:1504497
|
G | A | 1 | a0001c0002t0004g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.136-2894C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504497 | ||||||
chr5:1504597
|
A | C | 164 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0069others(161): Show | 170 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.136-2994T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504597 | ||||||
chr5:1504678
|
C | A | 20 | a0001c0001t0002g0087a0001c0001t0002g0124a0001c0001t0002g0133others(17): Show | 20 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.136-3075G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504678 | ||||||
chr5:1504678
|
C | T | 1 | a0002c0005t0003g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.136-3075G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504678 | ||||||
chr5:1504710
|
G | C | 1 | a0001c0001t0002g0144 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.136-3107C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504710 | ||||||
chr5:1504714
|
C | CA | 167 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(164): Show | 172 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.136-3112dupT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504714 | ||||||
chr5:1504714
|
C | CAA | 26 | a0001c0001t0002g0087a0001c0001t0002g0124a0001c0001t0002g0133others(23): Show | 26 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.136-3113_136-3112d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504714 | ||||||
chr5:1504714
|
CA | C | 9 | a0001c0001t0004g0106a0001c0001t0005g0026a0001c0001t0005g0265others(6): Show | 9 | HG02717.hp2 HG02723.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-3112delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504714 | ||||||
chr5:1504857
|
C | T | 3 | a0001c0001t0002g0124a0001c0002t0001g0156a0001c0002t0008g0155 | 3 | HG01106.hp2 HG01255.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.136-3254G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504857 | ||||||
chr5:1504870
|
G | C | 19 | a0001c0001t0002g0087a0001c0001t0002g0124a0001c0001t0002g0133others(16): Show | 19 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.136-3267C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504870 | ||||||
chr5:1504950
|
C | CCA | 3 | a0001c0001t0002g0124a0001c0002t0001g0156a0001c0002t0008g0155 | 3 | HG01106.hp2 HG01255.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.136-3349_136-3348d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504950 | ||||||
chr5:1504954
|
A | G | 3 | a0001c0001t0002g0124a0001c0002t0001g0156a0001c0002t0008g0155 | 3 | HG01106.hp2 HG01255.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.136-3351T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504954 | ||||||
chr5:1504954
|
AGTGTGGA others(66): Show |
A | 4 | a0001c0001t0007g0003a0001c0001t0007g0137a0001c0001t0007g0151others(1): Show | 5 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-3424_136-3352d others(75): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504954 | ||||||
chr5:1504981
|
C | T | 59 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0093others(56): Show | 62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-3378G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1504981 | ||||||
chr5:1505104
|
T | TGGAATAA others(64): Show |
6 | a0001c0001t0005g0358a0001c0001t0005g0359a0001c0004t0002g0115others(3): Show | 6 | HG00438.hp2 HG02015.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-3572_136-3502d others(73): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505104 | ||||||
chr5:1505127
|
C | T | 59 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0093others(56): Show | 62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-3524G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505127 | ||||||
chr5:1505129
|
C | G | 1 | a0001c0002t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136-3526G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505129 | ||||||
chr5:1505156
|
CACTGCTT others(62): Show |
C | 1 | a0001c0002t0001g0286 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.136-3622_136-3554d others(71): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505156 | ||||||
chr5:1505223
|
A | G | 1 | a0002c0005t0003g0332 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.136-3620T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505223 | ||||||
chr5:1505244
|
C | T | 5 | a0001c0001t0002g0087a0001c0001t0002g0242a0001c0001t0027g0274others(2): Show | 5 | HG02109.hp2 HG02895.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-3641G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505244 | ||||||
chr5:1505250
|
A | G | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-3647T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505250 | ||||||
chr5:1505258
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.136-3655T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505258 | ||||||
chr5:1505414
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.136-3811C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505414 | ||||||
chr5:1505474
|
A | G | 81 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0087others(78): Show | 84 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.136-3871T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505474 | ||||||
chr5:1505559
|
CCGGGT | C | 19 | a0001c0001t0002g0087a0001c0001t0002g0124a0001c0001t0002g0133others(16): Show | 19 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.136-3961_136-3957d others(7): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505559 | ||||||
chr5:1505560
|
CGGGTA | C | 230 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0028others(227): Show | 238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.136-3962_136-3958d others(7): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505560 | ||||||
chr5:1505565
|
A | T | 19 | a0001c0001t0002g0087a0001c0001t0002g0124a0001c0001t0002g0133others(16): Show | 19 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.136-3962T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505565 | ||||||
chr5:1505623
|
G | A | 59 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0093others(56): Show | 62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-4020C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505623 | ||||||
chr5:1505656
|
G | A | 7 | a0001c0002t0001g0074a0001c0002t0001g0244a0001c0002t0001g0252others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-4053C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505656 | ||||||
chr5:1505740
|
C | T | 1 | a0001c0002t0023g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-4137G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505740 | ||||||
chr5:1505749
|
T | C | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-4146A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505749 | ||||||
chr5:1505767
|
C | T | 1 | a0001c0003t0001g0071 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.136-4164G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505767 | ||||||
chr5:1505821
|
C | T | 85 | a0001c0001t0002g0069a0001c0001t0002g0113a0001c0001t0002g0162others(82): Show | 88 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.136-4218G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505821 | ||||||
chr5:1505843
|
C | T | 1 | a0001c0001t0002g0348 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.136-4240G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1505843 | ||||||
chr5:1506188
|
A | G | 59 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0093others(56): Show | 62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-4585T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506188 | ||||||
chr5:1506257
|
G | A | 3 | a0001c0001t0007g0095a0001c0004t0017g0015a0001c0004t0024g0033 | 3 | HG02145.hp2 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.136-4654C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506257 | ||||||
chr5:1506270
|
G | A | 59 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0093others(56): Show | 62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-4667C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506270 | ||||||
chr5:1506359
|
G | A | 74 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(71): Show | 76 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.136-4756C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506359 | ||||||
chr5:1506414
|
G | A | 2 | a0001c0002t0004g0098a0001c0002t0004g0150 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.136-4811C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506414 | ||||||
chr5:1506504
|
C | T | 59 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0093others(56): Show | 62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-4901G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506504 | ||||||
chr5:1506629
|
G | A | 1 | a0001c0003t0001g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.136-5026C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506629 | ||||||
chr5:1506804
|
C | T | 1 | a0001c0003t0001g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.136-5201G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506804 | ||||||
chr5:1506859
|
C | G | 5 | a0001c0002t0001g0217a0001c0003t0001g0215a0001c0003t0001g0251others(2): Show | 5 | HG01261.hp2 HG01981.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-5256G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1506859 | ||||||
chr5:1507101
|
C | T | 14 | a0001c0001t0002g0124a0001c0001t0002g0133a0001c0001t0002g0139others(11): Show | 14 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-5498G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507101 | ||||||
chr5:1507107
|
G | C | 59 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0093others(56): Show | 62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-5504C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507107 | ||||||
chr5:1507183
|
T | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0093a0001c0001t0002g0199others(8): Show | 12 | HG00423.hp2 HG00673.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-5580A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507183 | ||||||
chr5:1507199
|
G | T | 7 | a0001c0002t0001g0074a0001c0002t0001g0244a0001c0002t0001g0252others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-5596C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507199 | ||||||
chr5:1507212
|
G | A | 14 | a0001c0001t0002g0124a0001c0001t0002g0133a0001c0001t0002g0139others(11): Show | 14 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-5609C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507212 | ||||||
chr5:1507393
|
G | C | 59 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0093others(56): Show | 62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.136-5790C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507393 | ||||||
chr5:1507419
|
G | A | 1 | a0001c0003t0001g0002 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.136-5816C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507419 | ||||||
chr5:1507421
|
T | G | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.136-5818A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507421 | ||||||
chr5:1507532
|
T | C | 4 | a0001c0002t0001g0194a0001c0002t0001g0195a0001c0004t0005g0160others(1): Show | 4 | NA18983.hp2 NA19057.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-5929A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507532 | ||||||
chr5:1507547
|
C | G | 1 | a0001c0002t0023g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-5944G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507547 | ||||||
chr5:1507590
|
C | T | 1 | a0001c0002t0001g0360 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.136-5987G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507590 | ||||||
chr5:1507591
|
G | A | 1 | a0002c0006t0003g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136-5988C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507591 | ||||||
chr5:1507593
|
C | T | 2 | a0001c0003t0001g0281a0001c0004t0005g0290 | 2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136-5990G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507593 | ||||||
chr5:1507628
|
C | T | 1 | a0001c0003t0006g0174 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.136-6025G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507628 | ||||||
chr5:1507645
|
G | A | 2 | a0001c0002t0001g0165a0001c0002t0001g0166 | 2 | NA18994.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.136-6042C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507645 | ||||||
chr5:1507665
|
C | T | 1 | a0002c0005t0003g0116 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.136-6062G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507665 | ||||||
chr5:1507666
|
G | A | 1 | a0002c0005t0003g0013 | 2 | NA19010.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.136-6063C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507666 | ||||||
chr5:1507675
|
C | T | 3 | a0001c0001t0002g0113a0001c0001t0002g0284a0001c0001t0002g0285 | 3 | HG01891.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.136-6072G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507675 | ||||||
chr5:1507893
|
GAACTCCA others(10): Show |
G | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-6307_136-6291d others(19): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507893 | ||||||
chr5:1507991
|
G | C | 3 | a0001c0004t0002g0246a0001c0007t0007g0110a0004c0014t0034g0145 | 3 | HG01884.hp1 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.136-6388C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1507991 | ||||||
chr5:1508004
|
C | T | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.136-6401G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508004 | ||||||
chr5:1508144
|
C | T | 6 | a0001c0001t0002g0214a0001c0001t0025g0059a0001c0002t0001g0060others(3): Show | 6 | HG00735.hp2 NA18939.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-6541G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508144 | ||||||
chr5:1508145
|
A | G | 9 | a0001c0001t0002g0214a0001c0001t0025g0059a0001c0002t0001g0060others(6): Show | 9 | HG00735.hp2 NA18939.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-6542T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508145 | ||||||
chr5:1508155
|
T | C | 135 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0085others(132): Show | 142 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.136-6552A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508155 | ||||||
chr5:1508216
|
C | T | 1 | a0001c0007t0004g0256 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.136-6613G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508216 | ||||||
chr5:1508233
|
G | A | 88 | a0001c0001t0002g0058a0001c0001t0002g0085a0001c0001t0002g0162others(85): Show | 92 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.136-6630C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508233 | ||||||
chr5:1508281
|
T | A | 75 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(72): Show | 77 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.136-6678A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508281 | ||||||
chr5:1508440
|
T | A | 1 | a0001c0007t0007g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.136-6837A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508440 | ||||||
chr5:1508490
|
C | T | 2 | a0001c0001t0007g0003a0001c0001t0007g0151 | 3 | HG02896.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.136-6887G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508490 | ||||||
chr5:1508566
|
G | A | 3 | a0002c0006t0003g0031a0002c0006t0003g0032a0002c0006t0003g0142 | 3 | HG02965.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136-6963C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508566 | ||||||
chr5:1508722
|
T | C | 147 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(144): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.136-7119A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508722 | ||||||
chr5:1508862
|
C | T | 2 | a0003c0008t0002g0009a0003c0008t0002g0353 | 3 | HG00099.hp2 HG01516.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.136-7259G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508862 | ||||||
chr5:1508905
|
C | A | 1 | a0002c0005t0003g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.136-7302G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508905 | ||||||
chr5:1508983
|
C | T | 1 | a0002c0005t0003g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.136-7380G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1508983 | ||||||
chr5:1509030
|
G | A | 7 | a0001c0002t0001g0202a0001c0002t0006g0204a0001c0003t0001g0206others(4): Show | 7 | HG01070.hp1 HG01074.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-7427C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509030 | ||||||
chr5:1509031
|
C | T | 2 | a0001c0001t0004g0106a0001c0001t0007g0271 | 2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136-7428G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509031 | ||||||
chr5:1509078
|
T | C | 3 | a0001c0001t0002g0041a0001c0002t0001g0292a0001c0015t0004g0254 | 3 | HG00099.hp1 NA20752.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.136-7475A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509078 | ||||||
chr5:1509095
|
T | C | 4 | a0001c0003t0006g0172a0001c0003t0006g0207a0001c0003t0006g0208others(1): Show | 4 | HG00621.hp1 HG02040.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-7492A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509095 | ||||||
chr5:1509141
|
G | A | 1 | a0001c0003t0001g0336 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.136-7538C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509141 | ||||||
chr5:1509155
|
G | A | 1 | a0002c0005t0003g0243 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.136-7552C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509155 | ||||||
chr5:1509170
|
G | A | 15 | a0001c0001t0002g0113a0001c0003t0009g0235a0001c0004t0004g0260others(12): Show | 15 | HG00140.hp1 HG00733.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-7567C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509170 | ||||||
chr5:1509194
|
C | T | 1 | a0001c0003t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-7591G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509194 | ||||||
chr5:1509195
|
G | A | 1 | a0001c0002t0008g0333 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.136-7592C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509195 | ||||||
chr5:1509289
|
G | A | 1 | a0001c0004t0004g0211 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.136-7686C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509289 | ||||||
chr5:1509352
|
G | A | 2 | a0001c0001t0021g0248a0001c0002t0004g0094 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136-7749C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509352 | ||||||
chr5:1509397
|
G | A | 2 | a0001c0001t0007g0095a0001c0003t0009g0235 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.136-7794C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509397 | ||||||
chr5:1509432
|
G | C | 1 | a0001c0002t0001g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-7829C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509432 | ||||||
chr5:1509461
|
T | C | 80 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(77): Show | 83 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.136-7858A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509461 | ||||||
chr5:1509511
|
C | A | 1 | a0001c0001t0002g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.136-7908G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509511 | ||||||
chr5:1509528
|
C | A | 1 | a0001c0003t0001g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-7925G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509528 | ||||||
chr5:1509633
|
G | A | 2 | a0001c0001t0002g0361a0001c0002t0004g0143 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.136-8030C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509633 | ||||||
chr5:1509772
|
C | T | 4 | a0001c0002t0001g0286a0001c0002t0001g0287a0001c0002t0001g0289others(1): Show | 4 | HG02258.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-8169G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509772 | ||||||
chr5:1509789
|
T | C | 1 | a0001c0003t0009g0012 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.136-8186A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509789 | ||||||
chr5:1509815
|
G | C | 138 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(135): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.136-8212C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509815 | ||||||
chr5:1509836
|
G | A | 2 | a0001c0001t0004g0106a0001c0001t0007g0271 | 2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136-8233C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509836 | ||||||
chr5:1509849
|
G | C | 13 | a0001c0001t0002g0113a0001c0001t0004g0106a0001c0001t0007g0271others(10): Show | 13 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.136-8246C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509849 | ||||||
chr5:1509865
|
T | C | 1 | a0001c0003t0001g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-8262A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509865 | ||||||
chr5:1509903
|
G | A | 202 | a0001c0001t0002g0005a0001c0001t0002g0028a0001c0001t0002g0036others(199): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.136-8300C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1509903 | ||||||
chr5:1510082
|
GTTTC | G | 8 | a0001c0002t0001g0074a0001c0002t0001g0247a0001c0002t0001g0252others(5): Show | 8 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-8483_136-8480d others(6): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510082 | ||||||
chr5:1510200
|
G | A | 32 | a0001c0001t0002g0087a0001c0001t0002g0109a0001c0001t0002g0361others(29): Show | 33 | HG00140.hp1 HG01106.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.136-8597C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510200 | ||||||
chr5:1510226
|
C | G | 5 | a0001c0001t0002g0087a0001c0001t0002g0109a0001c0001t0007g0261others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-8623G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510226 | ||||||
chr5:1510257
|
T | A | 2 | a0001c0001t0025g0059a0001c0002t0001g0060 | 2 | NA18939.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.136-8654A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510257 | ||||||
chr5:1510350
|
G | A | 1 | a0001c0001t0007g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.136-8747C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510350 | ||||||
chr5:1510398
|
G | A | 3 | a0001c0001t0002g0113a0001c0002t0001g0276a0001c0002t0004g0273 | 3 | HG01891.hp2 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-8795C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510398 | ||||||
chr5:1510453
|
T | A | 3 | a0001c0001t0002g0085a0001c0002t0001g0250a0001c0003t0001g0345 | 3 | HG02523.hp1 NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.136-8850A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510453 | ||||||
chr5:1510506
|
A | G | 1 | a0001c0002t0001g0052 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.136-8903T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510506 | ||||||
chr5:1510695
|
G | A | 1 | a0001c0001t0002g0241 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.136-9092C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510695 | ||||||
chr5:1510772
|
A | G | 1 | a0001c0002t0001g0321 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.136-9169T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510772 | ||||||
chr5:1510925
|
C | T | 11 | a0001c0002t0001g0244a0001c0002t0023g0245a0001c0004t0002g0246others(8): Show | 11 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-9322G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510925 | ||||||
chr5:1510937
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.136-9334G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510937 | ||||||
chr5:1510938
|
G | A | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-9335C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1510938 | ||||||
chr5:1511017
|
C | T | 1 | a0003c0008t0002g0123 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.136-9414G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511017 | ||||||
chr5:1511107
|
C | T | 18 | a0001c0001t0007g0283a0001c0002t0001g0244a0001c0002t0023g0245others(15): Show | 18 | HG00140.hp1 HG01106.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.136-9504G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511107 | ||||||
chr5:1511169
|
G | A | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-9566C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511169 | ||||||
chr5:1511170
|
T | A | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-9567A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511170 | ||||||
chr5:1511246
|
G | A | 1 | a0001c0001t0004g0365 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.136-9643C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511246 | ||||||
chr5:1511261
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.136-9658C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511261 | ||||||
chr5:1511308
|
G | A | 1 | a0004c0014t0034g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.136-9705C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511308 | ||||||
chr5:1511363
|
C | T | 1 | a0001c0003t0006g0227 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.136-9760G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511363 | ||||||
chr5:1511410
|
A | ATGGGGAT others(62): Show |
67 | a0001c0001t0002g0005a0001c0001t0002g0093a0001c0001t0002g0222others(64): Show | 68 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.136-9808_136-9807i others(71): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511410 | ||||||
chr5:1511410
|
ATGGGGAT others(62): Show |
A | 6 | a0001c0001t0004g0106a0001c0001t0005g0265a0001c0001t0007g0271others(3): Show | 6 | HG02922.hp2 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-9876_136-9808d others(71): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511410 | ||||||
chr5:1511548
|
T | TTGGGGAT others(96): Show |
3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.136-9946_136-9945i others(105): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511548 | ||||||
chr5:1511582
|
G | A | 1 | a0001c0001t0004g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.136-9979C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511582 | ||||||
chr5:1511582
|
G | GTGGGGAC others(62): Show |
1 | a0001c0002t0001g0049 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.136-9980_136-9979i others(71): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511582 | ||||||
chr5:1511582
|
G | T | 1 | a0001c0002t0001g0304 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.136-9979C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511582 | ||||||
chr5:1511589
|
T | C | 1 | a0001c0001t0004g0081 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.136-9986A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511589 | ||||||
chr5:1511594
|
T | C | 1 | a0001c0002t0001g0304 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.136-9991A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511594 | ||||||
chr5:1511605
|
T | C | 1 | a0001c0002t0001g0304 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.136-10002A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511605 | ||||||
chr5:1511773
|
C | T | 2 | a0001c0007t0004g0220a0002c0005t0003g0363 | 2 | HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.136-10170G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511773 | ||||||
chr5:1511823
|
G | C | 3 | a0001c0001t0007g0095a0001c0002t0001g0278a0001c0004t0017g0015 | 3 | HG02145.hp2 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.136-10220C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1511823 | ||||||
chr5:1512092
|
C | T | 1 | a0001c0003t0006g0172 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.136-10489G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512092 | ||||||
chr5:1512093
|
G | A | 14 | a0001c0001t0007g0283a0001c0002t0001g0244a0001c0002t0023g0245others(11): Show | 14 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-10490C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512093 | ||||||
chr5:1512200
|
C | G | 2 | a0001c0001t0004g0134a0001c0003t0001g0251 | 2 | HG01168.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.136-10597G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512200 | ||||||
chr5:1512206
|
T | A | 3 | a0001c0001t0004g0365a0001c0001t0027g0274a0001c0002t0001g0364 | 3 | HG02886.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.136-10603A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512206 | ||||||
chr5:1512207
|
C | G | 22 | a0001c0001t0002g0087a0001c0001t0002g0109a0001c0001t0002g0113others(19): Show | 22 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.136-10604G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512207 | ||||||
chr5:1512382
|
T | C | 26 | a0001c0001t0002g0087a0001c0001t0002g0109a0001c0001t0002g0113others(23): Show | 27 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.136-10779A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512382 | ||||||
chr5:1512504
|
C | G | 1 | a0001c0003t0001g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-10901G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512504 | ||||||
chr5:1512538
|
C | G | 10 | a0001c0001t0002g0144a0001c0001t0002g0297a0001c0001t0005g0294others(7): Show | 10 | NA18939.hp2 NA18959.hp2 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-10935G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512538 | ||||||
chr5:1512613
|
T | C | 3 | a0001c0001t0004g0365a0001c0001t0027g0274a0001c0002t0001g0364 | 3 | HG02886.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.136-11010A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512613 | ||||||
chr5:1512627
|
C | T | 105 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0041others(102): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.136-11024G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512627 | ||||||
chr5:1512721
|
C | G | 1 | a0001c0001t0002g0361 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.135+10989G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512721 | ||||||
chr5:1512753
|
T | C | 208 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(205): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.135+10957A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512753 | ||||||
chr5:1512814
|
C | T | 2 | a0001c0001t0002g0041a0001c0015t0004g0254 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.135+10896G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512814 | ||||||
chr5:1512848
|
T | C | 1 | a0001c0001t0002g0361 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.135+10862A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512848 | ||||||
chr5:1512901
|
C | T | 1 | a0001c0002t0001g0360 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.135+10809G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512901 | ||||||
chr5:1512945
|
C | T | 1 | a0001c0001t0004g0223 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.135+10765G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512945 | ||||||
chr5:1512961
|
G | A | 1 | a0001c0019t0012g0280 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.135+10749C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512961 | ||||||
chr5:1512997
|
C | T | 8 | a0001c0001t0002g0113a0001c0001t0002g0262a0001c0002t0004g0098others(5): Show | 8 | HG01099.hp2 HG01261.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+10713G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1512997 | ||||||
chr5:1513041
|
A | T | 1 | a0002c0005t0003g0171 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.135+10669T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513041 | ||||||
chr5:1513194
|
C | T | 1 | a0001c0002t0002g0051 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.135+10516G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513194 | ||||||
chr5:1513308
|
C | G | 30 | a0001c0001t0002g0113a0001c0001t0002g0262a0001c0001t0002g0284others(27): Show | 30 | HG01099.hp2 HG01261.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.135+10402G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513308 | ||||||
chr5:1513399
|
G | A | 16 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0004g0011others(13): Show | 17 | HG01243.hp1 HG02145.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.135+10311C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513399 | ||||||
chr5:1513588
|
G | T | 22 | a0001c0001t0002g0069a0001c0001t0002g0076a0001c0001t0002g0096others(19): Show | 23 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.135+10122C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513588 | ||||||
chr5:1513628
|
G | A | 1 | a0001c0001t0002g0361 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.135+10082C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513628 | ||||||
chr5:1513636
|
C | G | 4 | a0001c0001t0002g0361a0001c0001t0007g0283a0001c0003t0001g0281others(1): Show | 4 | HG01496.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+10074G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513636 | ||||||
chr5:1513647
|
T | C | 1 | a0001c0002t0001g0321 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.135+10063A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513647 | ||||||
chr5:1513648
|
GTTTCCTC others(47): Show |
G | 4 | a0001c0001t0004g0106a0001c0001t0007g0271a0001c0003t0009g0239others(1): Show | 4 | HG02717.hp2 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+10008_135+1006 others(58): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513648 | ||||||
chr5:1513702
|
A | G | 4 | a0001c0002t0001g0286a0001c0002t0001g0287a0001c0002t0001g0289others(1): Show | 4 | HG02258.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+10008T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513702 | ||||||
chr5:1513773
|
G | A | 59 | a0001c0001t0002g0041a0001c0001t0002g0222a0001c0001t0002g0297others(56): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.135+9937C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513773 | ||||||
chr5:1513784
|
T | C | 2 | a0001c0003t0001g0268a0001c0003t0001g0269 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.135+9926A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513784 | ||||||
chr5:1513819
|
G | C | 2 | a0001c0003t0001g0268a0001c0003t0001g0269 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.135+9891C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513819 | ||||||
chr5:1513823
|
A | G | 2 | a0001c0003t0001g0268a0001c0003t0001g0269 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.135+9887T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513823 | ||||||
chr5:1513827
|
G | A | 55 | a0001c0001t0002g0041a0001c0001t0002g0222a0001c0001t0002g0297others(52): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.135+9883C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513827 | ||||||
chr5:1513862
|
A | G | 2 | a0001c0003t0001g0268a0001c0003t0001g0269 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.135+9848T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513862 | ||||||
chr5:1513916
|
G | A | 10 | a0001c0001t0002g0255a0001c0004t0004g0210a0001c0004t0004g0211others(7): Show | 10 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+9794C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513916 | ||||||
chr5:1513918
|
A | G | 1 | a0001c0003t0009g0012 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+9792T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513918 | ||||||
chr5:1513956
|
C | G | 1 | a0001c0003t0009g0012 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+9754G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513956 | ||||||
chr5:1513970
|
G | A | 1 | a0001c0001t0004g0365 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.135+9740C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513970 | ||||||
chr5:1513982
|
G | A | 2 | a0001c0001t0005g0026a0001c0002t0001g0025 | 2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.135+9728C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513982 | ||||||
chr5:1513995
|
C | T | 8 | a0001c0001t0002g0113a0001c0001t0002g0262a0001c0002t0004g0098others(5): Show | 8 | HG01099.hp2 HG01261.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+9715G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513995 | ||||||
chr5:1513996
|
A | G | 34 | a0001c0001t0002g0113a0001c0001t0002g0262a0001c0001t0002g0284others(31): Show | 34 | HG01099.hp2 HG01261.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.135+9714T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1513996 | ||||||
chr5:1514045
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135+9665T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514045 | ||||||
chr5:1514091
|
C | A | 3 | a0001c0001t0004g0365a0001c0001t0027g0274a0001c0002t0001g0364 | 3 | HG02886.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.135+9619G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514091 | ||||||
chr5:1514324
|
C | T | 1 | a0001c0010t0001g0275 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.135+9386G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514324 | ||||||
chr5:1514339
|
G | A | 27 | a0001c0001t0002g0255a0001c0002t0001g0074a0001c0002t0001g0244others(24): Show | 27 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.135+9371C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514339 | ||||||
chr5:1514347
|
A | G | 191 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(188): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.135+9363T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514347 | ||||||
chr5:1514522
|
G | A | 101 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(98): Show | 106 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.135+9188C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514522 | ||||||
chr5:1514666
|
T | C | 1 | a0002c0005t0003g0149 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.135+9044A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514666 | ||||||
chr5:1514705
|
C | T | 2 | a0001c0001t0004g0106a0001c0001t0007g0271 | 2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.135+9005G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514705 | ||||||
chr5:1514715
|
A | G | 49 | a0001c0001t0002g0028a0001c0001t0002g0113a0001c0001t0002g0262others(46): Show | 50 | HG01099.hp2 HG01243.hp1 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.135+8995T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514715 | ||||||
chr5:1514781
|
T | C | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.135+8929A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514781 | ||||||
chr5:1514797
|
A | G | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.135+8913T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514797 | ||||||
chr5:1514908
|
A | C | 1 | a0002c0005t0003g0355 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.135+8802T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514908 | ||||||
chr5:1514965
|
G | A | 4 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0003t0009g0239others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+8745C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1514965 | ||||||
chr5:1515066
|
ACCCCCAG others(89): Show |
A | 4 | a0001c0001t0002g0361a0001c0002t0001g0244a0001c0002t0023g0245others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+8548_135+8643d others(98): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515066 | ||||||
chr5:1515072
|
A | G | 2 | a0001c0001t0005g0026a0001c0002t0001g0025 | 2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.135+8638T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515072 | ||||||
chr5:1515123
|
T | C | 59 | a0001c0001t0002g0041a0001c0001t0002g0113a0001c0001t0002g0255others(56): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.135+8587A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515123 | ||||||
chr5:1515123
|
TGGCCCTT others(89): Show |
T | 1 | a0001c0001t0002g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.135+8491_135+8586d others(98): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515123 | ||||||
chr5:1515219
|
C | T | 15 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0005g0167others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+8491G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515219 | ||||||
chr5:1515278
|
C | T | 1 | a0001c0003t0001g0272 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.135+8432G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515278 | ||||||
chr5:1515367
|
G | C | 2 | a0001c0002t0008g0334a0001c0002t0008g0335 | 2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.135+8343C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515367 | ||||||
chr5:1515420
|
G | C | 120 | a0001c0001t0002g0041a0001c0001t0002g0109a0001c0001t0002g0113others(117): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.135+8290C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515420 | ||||||
chr5:1515539
|
G | A | 1 | a0002c0005t0003g0149 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.135+8171C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515539 | ||||||
chr5:1515672
|
A | G | 59 | a0001c0001t0002g0113a0001c0001t0002g0255a0001c0001t0002g0262others(56): Show | 60 | HG01099.hp2 HG01106.hp1 HG01256.hp1 others(57): Show |
intron_variant | MODIFIER | c.135+8038T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515672 | ||||||
chr5:1515706
|
A | T | 1 | a0001c0002t0001g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.135+8004T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515706 | ||||||
chr5:1515744
|
C | T | 1 | a0002c0005t0003g0149 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.135+7966G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515744 | ||||||
chr5:1515768
|
T | A | 82 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(79): Show | 86 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.135+7942A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515768 | ||||||
chr5:1515874
|
C | G | 1 | a0001c0001t0002g0044 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.135+7836G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515874 | ||||||
chr5:1515894
|
G | A | 2 | a0001c0001t0007g0003a0001c0001t0007g0151 | 3 | HG02896.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.135+7816C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515894 | ||||||
chr5:1515979
|
G | A | 60 | a0001c0001t0002g0041a0001c0001t0002g0222a0001c0001t0002g0297others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.135+7731C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1515979 | ||||||
chr5:1516041
|
A | G | 3 | a0001c0001t0011g0326a0001c0003t0001g0327a0001c0003t0033g0352 | 3 | HG00597.hp2 HG02129.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.135+7669T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516041 | ||||||
chr5:1516123
|
G | A | 1 | a0001c0001t0007g0080 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.135+7587C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516123 | ||||||
chr5:1516252
|
G | A | 1 | a0001c0001t0004g0349 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.135+7458C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516252 | ||||||
chr5:1516299
|
T | A | 33 | a0001c0001t0002g0113a0001c0001t0002g0262a0001c0001t0002g0284others(30): Show | 34 | HG01099.hp2 HG01261.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.135+7411A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516299 | ||||||
chr5:1516422
|
G | A | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.135+7288C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516422 | ||||||
chr5:1516461
|
C | T | 1 | a0001c0002t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.135+7249G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516461 | ||||||
chr5:1516468
|
G | C | 2 | a0001c0001t0007g0261a0001c0007t0007g0110 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.135+7242C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516468 | ||||||
chr5:1516632
|
C | CT | 36 | a0001c0001t0002g0113a0001c0001t0002g0262a0001c0001t0002g0284others(33): Show | 37 | HG01099.hp2 HG01261.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.135+7077dupA | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516632 | ||||||
chr5:1516632
|
CT | C | 8 | a0001c0001t0007g0095a0001c0002t0001g0067a0001c0002t0001g0068others(5): Show | 8 | HG01069.hp2 HG01928.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+7077delA | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516632 | ||||||
chr5:1516770
|
C | G | 55 | a0001c0001t0002g0109a0001c0001t0002g0222a0001c0001t0002g0297others(52): Show | 55 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.135+6940G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516770 | ||||||
chr5:1516886
|
G | C | 4 | a0001c0001t0002g0109a0001c0001t0007g0261a0001c0003t0009g0039others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+6824C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1516886 | ||||||
chr5:1517009
|
C | T | 4 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0003t0009g0239others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+6701G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517009 | ||||||
chr5:1517083
|
C | T | 58 | a0001c0001t0002g0109a0001c0001t0002g0222a0001c0001t0002g0297others(55): Show | 58 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.135+6627G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517083 | ||||||
chr5:1517124
|
T | A | 20 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0004g0106others(17): Show | 20 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+6586A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517124 | ||||||
chr5:1517161
|
G | A | 3 | a0001c0001t0007g0095a0001c0002t0001g0278a0001c0004t0017g0015 | 3 | HG02145.hp2 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.135+6549C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517161 | ||||||
chr5:1517200
|
C | A | 5 | a0001c0001t0002g0041a0001c0001t0004g0042a0001c0001t0004g0223others(2): Show | 5 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+6510G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517200 | ||||||
chr5:1517207
|
T | G | 206 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(203): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.135+6503A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517207 | ||||||
chr5:1517215
|
A | T | 1 | a0001c0002t0001g0218 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.135+6495T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517215 | ||||||
chr5:1517216
|
C | A | 1 | a0001c0002t0001g0218 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.135+6494G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517216 | ||||||
chr5:1517370
|
C | T | 1 | a0001c0003t0006g0157 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.135+6340G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517370 | ||||||
chr5:1517430
|
C | T | 33 | a0001c0001t0002g0113a0001c0001t0002g0262a0001c0001t0002g0284others(30): Show | 34 | HG01099.hp2 HG01261.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.135+6280G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517430 | ||||||
chr5:1517433
|
C | T | 1 | a0001c0003t0009g0012 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+6277G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517433 | ||||||
chr5:1517466
|
C | T | 1 | a0001c0003t0001g0002 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.135+6244G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517466 | ||||||
chr5:1517518
|
T | C | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135+6192A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517518 | ||||||
chr5:1517527
|
A | G | 103 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(100): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.135+6183T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517527 | ||||||
chr5:1517542
|
C | T | 1 | a0001c0001t0027g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.135+6168G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517542 | ||||||
chr5:1517586
|
T | C | 169 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(166): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.135+6124A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517586 | ||||||
chr5:1517599
|
A | C | 169 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(166): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.135+6111T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517599 | ||||||
chr5:1517654
|
C | T | 166 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(163): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.135+6056G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517654 | ||||||
chr5:1517661
|
T | C | 1 | a0001c0001t0007g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.135+6049A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517661 | ||||||
chr5:1517676
|
C | CAA | 103 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(100): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.135+6032_135+6033d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517676 | ||||||
chr5:1517677
|
A | C | 114 | a0001c0001t0002g0085a0001c0001t0002g0162a0001c0001t0002g0163others(111): Show | 121 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.135+6033T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517677 | ||||||
chr5:1517766
|
T | C | 59 | a0001c0001t0002g0087a0001c0001t0002g0222a0001c0001t0002g0297others(56): Show | 60 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.135+5944A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517766 | ||||||
chr5:1517768
|
G | A | 1 | a0001c0004t0005g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.135+5942C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517768 | ||||||
chr5:1517787
|
G | A | 1 | a0001c0001t0002g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+5923C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517787 | ||||||
chr5:1517853
|
C | G | 1 | a0001c0003t0009g0012 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+5857G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517853 | ||||||
chr5:1517866
|
C | A | 1 | a0001c0001t0004g0010 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.135+5844G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517866 | ||||||
chr5:1517868
|
C | G | 92 | a0001c0001t0002g0109a0001c0001t0002g0113a0001c0001t0002g0222others(89): Show | 93 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.135+5842G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517868 | ||||||
chr5:1517889
|
A | G | 3 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0006t0038g0370 | 3 | NA18956.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.135+5821T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517889 | ||||||
chr5:1517920
|
C | T | 9 | a0001c0001t0005g0265a0001c0001t0007g0283a0001c0003t0001g0281others(6): Show | 9 | HG01496.hp1 HG02451.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+5790G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517920 | ||||||
chr5:1517938
|
T | A | 1 | a0001c0003t0009g0012 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+5772A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1517938 | ||||||
chr5:1518102
|
C | T | 11 | a0001c0001t0002g0096a0001c0001t0002g0124a0001c0001t0002g0125others(8): Show | 11 | HG00280.hp1 HG00735.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+5608G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518102 | ||||||
chr5:1518244
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.135+5466G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518244 | ||||||
chr5:1518320
|
G | A | 2 | a0002c0005t0004g0146a0002c0016t0003g0147 | 2 | HG00733.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.135+5390C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518320 | ||||||
chr5:1518369
|
C | T | 3 | a0001c0001t0005g0265a0001c0010t0001g0266a0001c0020t0001g0267 | 3 | HG02922.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+5341G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518369 | ||||||
chr5:1518376
|
T | A | 184 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(181): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.135+5334A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518376 | ||||||
chr5:1518379
|
C | T | 16 | a0001c0001t0002g0222a0001c0001t0002g0297a0001c0001t0002g0300others(13): Show | 16 | HG00408.hp2 HG00639.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+5331G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518379 | ||||||
chr5:1518397
|
G | C | 1 | a0001c0010t0001g0275 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.135+5313C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518397 | ||||||
chr5:1518426
|
C | T | 53 | a0001c0001t0002g0222a0001c0001t0002g0297a0001c0001t0002g0300others(50): Show | 53 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.135+5284G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518426 | ||||||
chr5:1518486
|
A | G | 213 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(210): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.135+5224T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518486 | ||||||
chr5:1518511
|
T | C | 3 | a0001c0001t0005g0265a0001c0010t0001g0266a0001c0020t0001g0267 | 3 | HG02922.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+5199A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518511 | ||||||
chr5:1518572
|
C | T | 18 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0007g0283others(15): Show | 18 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.135+5138G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518572 | ||||||
chr5:1518577
|
T | C | 1 | a0001c0004t0005g0290 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.135+5133A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518577 | ||||||
chr5:1518583
|
G | A | 4 | a0001c0001t0028g0350a0001c0003t0001g0148a0001c0007t0004g0220others(1): Show | 4 | HG00639.hp1 HG01346.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+5127C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518583 | ||||||
chr5:1518604
|
T | C | 1 | a0001c0001t0002g0322 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.135+5106A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518604 | ||||||
chr5:1518679
|
C | T | 1 | a0001c0003t0009g0012 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.135+5031G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518679 | ||||||
chr5:1518740
|
G | T | 5 | a0001c0001t0002g0109a0001c0001t0007g0261a0001c0001t0027g0274others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+4970C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518740 | ||||||
chr5:1518774
|
G | A | 21 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0361others(18): Show | 21 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+4936C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518774 | ||||||
chr5:1518797
|
G | C | 1 | a0001c0002t0001g0278 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.135+4913C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518797 | ||||||
chr5:1518804
|
G | A | 1 | a0001c0004t0005g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.135+4906C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518804 | ||||||
chr5:1518830
|
T | C | 2 | a0001c0002t0004g0098a0001c0002t0004g0150 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.135+4880A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518830 | ||||||
chr5:1518908
|
G | A | 2 | a0001c0001t0004g0106a0001c0001t0007g0271 | 2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.135+4802C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518908 | ||||||
chr5:1518964
|
C | T | 38 | a0001c0001t0002g0038a0001c0001t0002g0222a0001c0001t0002g0297others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.135+4746G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1518964 | ||||||
chr5:1519016
|
G | A | 1 | a0001c0004t0002g0264 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.135+4694C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519016 | ||||||
chr5:1519082
|
T | C | 17 | a0001c0001t0002g0076a0001c0001t0002g0255a0001c0001t0004g0077others(14): Show | 19 | HG00738.hp1 HG01106.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.135+4628A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519082 | ||||||
chr5:1519149
|
A | G | 17 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0004g0011others(14): Show | 18 | HG01243.hp1 HG02145.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.135+4561T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519149 | ||||||
chr5:1519202
|
T | C | 1 | a0001c0002t0001g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.135+4508A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519202 | ||||||
chr5:1519307
|
A | G | 2 | a0001c0003t0001g0268a0001c0003t0001g0269 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.135+4403T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519307 | ||||||
chr5:1519389
|
T | C | 2 | a0001c0001t0007g0080a0001c0002t0001g0278 | 2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.135+4321A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519389 | ||||||
chr5:1519475
|
C | T | 1 | a0001c0004t0002g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.135+4235G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519475 | ||||||
chr5:1519503
|
T | A | 4 | a0001c0002t0001g0252a0001c0002t0001g0253a0001c0002t0001g0279others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+4207A>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519503 | ||||||
chr5:1519534
|
T | C | 7 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0002t0001g0244others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+4176A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519534 | ||||||
chr5:1519578
|
G | A | 121 | a0001c0001t0002g0093a0001c0001t0002g0162a0001c0001t0002g0163others(118): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.135+4132C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519578 | ||||||
chr5:1519710
|
C | T | 4 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0026g0022others(1): Show | 4 | HG01081.hp2 HG01109.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+4000G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519710 | ||||||
chr5:1519718
|
T | C | 25 | a0001c0001t0002g0222a0001c0001t0002g0255a0001c0001t0004g0223others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.135+3992A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519718 | ||||||
chr5:1519755
|
C | T | 4 | a0001c0001t0004g0106a0001c0003t0009g0235a0001c0007t0005g0104others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3955G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519755 | ||||||
chr5:1519912
|
G | C | 5 | a0001c0001t0005g0358a0001c0001t0005g0359a0001c0004t0002g0357others(2): Show | 5 | HG00438.hp2 HG02015.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+3798C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519912 | ||||||
chr5:1519974
|
T | G | 1 | a0001c0001t0002g0082 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.135+3736A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519974 | ||||||
chr5:1519990
|
G | A | 7 | a0001c0001t0002g0225a0001c0001t0002g0226a0001c0001t0002g0229others(4): Show | 7 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+3720C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1519990 | ||||||
chr5:1520095
|
T | C | 1 | a0001c0002t0001g0232 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.135+3615A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520095 | ||||||
chr5:1520100
|
G | A | 2 | a0001c0001t0002g0361a0001c0002t0001g0360 | 2 | HG00323.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.135+3610C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520100 | ||||||
chr5:1520317
|
C | T | 1 | a0001c0004t0005g0296 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.135+3393G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520317 | ||||||
chr5:1520326
|
G | T | 1 | a0001c0001t0005g0293 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.135+3384C>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520326 | ||||||
chr5:1520470
|
G | A | 4 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0005t0037g0371others(1): Show | 4 | NA18956.hp1 NA18970.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3240C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520470 | ||||||
chr5:1520499
|
G | A | 1 | a0001c0003t0006g0233 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.135+3211C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520499 | ||||||
chr5:1520507
|
T | C | 1 | a0001c0002t0001g0234 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.135+3203A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520507 | ||||||
chr5:1520550
|
C | G | 176 | a0001c0001t0002g0005a0001c0001t0002g0087a0001c0001t0002g0093others(173): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.135+3160G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520550 | ||||||
chr5:1520583
|
G | A | 6 | a0001c0001t0021g0248a0001c0002t0001g0244a0001c0002t0001g0247others(3): Show | 7 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+3127C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520583 | ||||||
chr5:1520643
|
A | C | 2 | a0001c0001t0002g0087a0001c0003t0001g0088 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.135+3067T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520643 | ||||||
chr5:1520695
|
C | T | 1 | a0001c0004t0005g0103 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.135+3015G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520695 | ||||||
chr5:1520795
|
A | G | 296 | a0001c0001t0002g0005a0001c0001t0002g0028a0001c0001t0002g0036others(293): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.135+2915T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520795 | ||||||
chr5:1520801
|
T | C | 1 | a0001c0002t0001g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.135+2909A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520801 | ||||||
chr5:1520817
|
C | T | 1 | a0001c0002t0001g0292 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.135+2893G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520817 | ||||||
chr5:1520818
|
G | A | 2 | a0001c0003t0014g0016a0001c0003t0014g0017 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.135+2892C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520818 | ||||||
chr5:1520820
|
A | G | 4 | a0001c0003t0016g0368a0001c0003t0016g0369a0002c0005t0037g0371others(1): Show | 4 | NA18956.hp1 NA18970.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+2890T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520820 | ||||||
chr5:1520860
|
C | CA | 15 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0362others(12): Show | 15 | HG00741.hp2 HG01496.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+2849dupT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520860 | ||||||
chr5:1520860
|
CA | C | 19 | a0001c0001t0002g0085a0001c0001t0002g0238a0001c0001t0005g0265others(16): Show | 19 | HG02145.hp2 HG02523.hp2 HG02735.hp2 others(16): Show |
intron_variant | MODIFIER | c.135+2849delT | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520860 | ||||||
chr5:1520860
|
CAA | C | 223 | a0001c0001t0002g0005a0001c0001t0002g0028a0001c0001t0002g0036others(220): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.135+2848_135+2849d others(4): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520860 | ||||||
chr5:1520860
|
CAAA | C | 14 | a0001c0001t0002g0096a0001c0001t0021g0248a0001c0002t0001g0244others(11): Show | 15 | HG01070.hp2 HG01074.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+2847_135+2849d others(5): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520860 | ||||||
chr5:1520876
|
A | AG | 4 | a0001c0001t0002g0262a0001c0001t0007g0261a0001c0004t0002g0263others(1): Show | 4 | HG01261.hp1 HG02559.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+2833_135+2834i others(3): Show |
LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1520876 | ||||||
chr5:1521130
|
T | C | 3 | a0001c0001t0004g0365a0001c0002t0001g0364a0001c0004t0005g0290 | 3 | HG02886.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.135+2580A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521130 | ||||||
chr5:1521147
|
C | G | 7 | a0001c0001t0002g0255a0001c0004t0004g0260a0001c0007t0004g0256others(4): Show | 7 | HG00099.hp1 HG01106.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+2563G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521147 | ||||||
chr5:1521273
|
C | A | 1 | a0001c0001t0002g0241 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.135+2437G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521273 | ||||||
chr5:1521302
|
C | T | 1 | a0001c0002t0001g0292 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.135+2408G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521302 | ||||||
chr5:1521313
|
C | T | 1 | a0001c0002t0001g0291 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.135+2397G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521313 | ||||||
chr5:1521332
|
A | G | 2 | a0001c0003t0014g0016a0001c0003t0014g0017 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.135+2378T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521332 | ||||||
chr5:1521361
|
T | C | 1 | a0001c0001t0021g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135+2349A>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521361 | ||||||
chr5:1521384
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135+2326C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521384 | ||||||
chr5:1521393
|
A | G | 2 | a0001c0001t0007g0095a0001c0004t0017g0015 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.135+2317T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521393 | ||||||
chr5:1521458
|
C | T | 86 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(83): Show | 90 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.135+2252G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521458 | ||||||
chr5:1521778
|
A | G | 75 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(72): Show | 78 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.135+1932T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521778 | ||||||
chr5:1521955
|
A | T | 2 | a0001c0003t0014g0016a0001c0003t0014g0017 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.135+1755T>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1521955 | ||||||
chr5:1522038
|
C | T | 1 | a0001c0002t0004g0094 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.135+1672G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522038 | ||||||
chr5:1522354
|
C | G | 1 | a0001c0002t0001g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.135+1356G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522354 | ||||||
chr5:1522371
|
T | G | 74 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(71): Show | 77 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.135+1339A>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522371 | ||||||
chr5:1522374
|
C | T | 74 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(71): Show | 77 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.135+1336G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522374 | ||||||
chr5:1522425
|
C | A | 1 | a0002c0005t0003g0243 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.135+1285G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522425 | ||||||
chr5:1522463
|
C | G | 3 | a0001c0001t0002g0093a0001c0003t0001g0091a0001c0003t0001g0092 | 3 | NA18952.hp2 NA18994.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.135+1247G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522463 | ||||||
chr5:1522465
|
G | C | 2 | a0001c0001t0002g0087a0001c0003t0001g0088 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.135+1245C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522465 | ||||||
chr5:1522620
|
G | C | 82 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(79): Show | 86 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.135+1090C>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1522620 | ||||||
chr5:1523036
|
G | A | 2 | a0001c0002t0001g0250a0002c0006t0032g0249 | 2 | NA18942.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.135+674C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523036 | ||||||
chr5:1523137
|
C | A | 1 | a0001c0003t0001g0251 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.135+573G>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523137 | ||||||
chr5:1523206
|
A | C | 295 | a0001c0001t0002g0005a0001c0001t0002g0028a0001c0001t0002g0036others(292): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.135+504T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523206 | ||||||
chr5:1523241
|
G | A | 2 | a0001c0001t0004g0365a0001c0002t0001g0364 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.135+469C>T | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523241 | ||||||
chr5:1523306
|
A | C | 1 | a0001c0002t0001g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.135+404T>G | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523306 | ||||||
chr5:1523396
|
C | T | 2 | a0001c0003t0001g0089a0001c0003t0001g0090 | 2 | NA18983.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.135+314G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523396 | ||||||
chr5:1523428
|
C | G | 76 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0038others(73): Show | 79 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.135+282G>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523428 | ||||||
chr5:1523518
|
A | G | 252 | a0001c0001t0002g0005a0001c0001t0002g0028a0001c0001t0002g0036others(249): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.135+192T>C | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523518 | ||||||
chr5:1523697
|
C | T | 1 | a0001c0001t0018g0018 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.135+13G>A | LPCAT1 | ENSG00000153395.10 | transcript | ENST00000283415.4 | protein_coding | 1/13 | chr5 | 1523697 |