geneid | 240 |
---|---|
ensemblid | ENSG00000012779.12 |
hgncid | 435 |
symbol | ALOX5 |
name | arachidonate 5-lipoxygenase |
refseq_nuc | NM_000698.5 |
refseq_prot | NP_000689.1 |
ensembl_nuc | ENST00000374391.7 |
ensembl_prot | ENSP00000363512.2 |
mane_status | MANE Select |
chr | chr10 |
start | 45374216 |
end | 45446117 |
strand | + |
ver | v1.2 |
region | chr10:45374216-45446117 |
region5000 | chr10:45369216-45451117 |
regionname0 | ALOX5_chr10_45374216_45446117 |
regionname5000 | ALOX5_chr10_45369216_45451117 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 674 | 321 | 86 | 53 | 136 | 14 | 31 | 111 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0002 | 0/0 | 674 | 16 | 5 | 1 | 9 | 0 | 1 | 6 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0003 | 0/0 | 674 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0004 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0005 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0006 | 0/0 | 370 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0007 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0008 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0009 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
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 | 0/1 | 2025 | 172 | 30 | 33 | 77 | 6 | 25 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0002 | 0/0 | 2025 | 57 | 11 | 9 | 27 | 5 | 5 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0003 | 0/0 | 2025 | 36 | 23 | 5 | 8 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0004 | 0/0 | 2025 | 31 | 11 | 2 | 16 | 2 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0005 | 0/0 | 2025 | 16 | 5 | 1 | 9 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0006 | 0/0 | 2025 | 7 | 6 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0007 | 0/0 | 2025 | 6 | 0 | 0 | 6 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0008 | 0/0 | 2025 | 3 | 2 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0009 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0010 | 0/0 | 2025 | 2 | 0 | 0 | 0 | 0 | 2 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0011 | 0/0 | 2025 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0012 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0013 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0014 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0015 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0016 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0017 | 0/0 | 2014 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0018 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0019 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0020 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0021 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
c0022 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 495 | 248 | 69 | 36 | 107 | 9 | 26 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
t0002 | 0/0 | 495 | 63 | 16 | 13 | 25 | 5 | 4 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
t0003 | 0/0 | 495 | 17 | 6 | 1 | 9 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
t0004 | 0/0 | 493 | 9 | 0 | 3 | 6 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
t0005 | 0/0 | 495 | 2 | 0 | 1 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
t0006 | 0/0 | 495 | 2 | 0 | 0 | 0 | 0 | 2 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
t0007 | 0/0 | 493 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
t0008 | 0/0 | 495 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
t0009 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
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 | 0/1 | 2025 | 172 | 30 | 33 | 77 | 6 | 25 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0002 | 0/0 | 2025 | 57 | 11 | 9 | 27 | 5 | 5 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0003 | 0/0 | 2025 | 36 | 23 | 5 | 8 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0004 | 0/0 | 2025 | 31 | 11 | 2 | 16 | 2 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0006 | 0/0 | 2025 | 7 | 6 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0007 | 0/0 | 2025 | 6 | 0 | 0 | 6 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0008 | 0/0 | 2025 | 3 | 2 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0009 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0011 | 0/0 | 2025 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0015 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0019 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0020 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0021 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0022 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0002c0005 | 0/0 | 2025 | 16 | 5 | 1 | 9 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0003c0010 | 0/0 | 2025 | 2 | 0 | 0 | 0 | 0 | 2 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0004c0012 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0005c0016 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0006c0013 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0007c0017 | 0/0 | 2014 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0008c0018 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0009c0014 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2519 | 166 | 28 | 32 | 75 | 6 | 24 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0001t0002 | 0/0 | 2519 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0001t0004 | 0/0 | 2517 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0001t0005 | 0/0 | 2519 | 2 | 0 | 1 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0001t0008 | 0/0 | 2519 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0002t0002 | 0/0 | 2519 | 54 | 11 | 9 | 25 | 5 | 4 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0002t0006 | 0/0 | 2519 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0002t0007 | 0/0 | 2517 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0003t0001 | 0/0 | 2519 | 26 | 21 | 2 | 3 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0003t0002 | 0/0 | 2519 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0003t0003 | 0/0 | 2519 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0003t0004 | 0/0 | 2517 | 8 | 0 | 3 | 5 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0004t0001 | 0/0 | 2519 | 31 | 11 | 2 | 16 | 2 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0006t0001 | 0/0 | 2519 | 6 | 5 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0006t0009 | 0/0 | 2519 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0007t0001 | 0/0 | 2519 | 6 | 0 | 0 | 6 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0008t0002 | 0/0 | 2519 | 3 | 2 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0009t0001 | 0/0 | 2519 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0011t0002 | 0/0 | 2519 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0015t0001 | 0/0 | 2519 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0019t0001 | 0/0 | 2519 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0020t0001 | 0/0 | 2519 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0021t0006 | 0/0 | 2519 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0001c0022t0002 | 0/0 | 2519 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0002c0005t0003 | 0/0 | 2519 | 16 | 5 | 1 | 9 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0003c0010t0001 | 0/0 | 2519 | 2 | 0 | 0 | 0 | 0 | 2 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0004c0012t0001 | 0/0 | 2519 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0005c0016t0001 | 0/0 | 2519 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0006c0013t0001 | 0/0 | 2519 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0007c0017t0001 | 0/0 | 2508 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0008c0018t0001 | 0/0 | 2519 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
a0009c0014t0001 | 0/0 | 2519 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | copy fasta | chr10 | 45369216 | 45451117 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0001t0008g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0006g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0007g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0002t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0006t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0006t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0006t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0006t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0006t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0006t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0007t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0007t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0007t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0007t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0007t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0008t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0008t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0008t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0009t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0009t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0011t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0011t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0015t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0019t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0020t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0021t0006g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0001c0022t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0002c0005t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0003c0010t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0003c0010t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0004c0012t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0005c0016t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0006c0013t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0007c0017t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0008c0018t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
a0009c0014t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0297 | EUR | GBR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0276 | EUR | GBR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00280 | hp2 | a0001 | c0004 | t0001 | g0202 | EUR | FIN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0293 | EUR | FIN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00408 | hp1 | a0001 | c0004 | t0001 | g0020 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00642 | hp2 | a0001 | c0022 | t0002 | g0275 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG00741 | hp2 | a0001 | c0011 | t0002 | g0258 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0267 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0266 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0145 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01109 | hp1 | a0001 | c0008 | t0002 | g0312 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01167 | hp1 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01169 | hp1 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0294 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01192 | hp2 | a0001 | c0011 | t0002 | g0257 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0310 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01243 | hp2 | a0002 | c0005 | t0003 | g0040 | AMR | PUR | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0174 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01261 | hp2 | a0001 | c0003 | t0004 | g0048 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0076 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0279 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0027 | EUR | IBS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01517 | hp1 | a0001 | c0004 | t0001 | g0168 | EUR | IBS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0027 | EUR | IBS | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0288 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01884 | hp2 | a0001 | c0006 | t0001 | g0005 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0287 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01928 | hp2 | a0001 | c0003 | t0004 | g0054 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01993 | hp1 | a0001 | c0003 | t0004 | g0047 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0268 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0295 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02040 | hp1 | a0002 | c0005 | t0003 | g0156 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02056 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02080 | hp2 | a0002 | c0005 | t0003 | g0123 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02155 | hp1 | a0002 | c0005 | t0003 | g0122 | EAS | CDX | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0055 | EAS | CDX | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02258 | hp1 | a0001 | c0004 | t0001 | g0007 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02258 | hp2 | a0006 | c0013 | t0001 | g0253 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02451 | hp2 | a0001 | c0006 | t0001 | g0005 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02572 | hp1 | a0001 | c0009 | t0001 | g0140 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0285 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0289 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02647 | hp2 | a0002 | c0005 | t0003 | g0158 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02698 | hp1 | a0001 | c0021 | t0006 | g0291 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02717 | hp1 | a0001 | c0009 | t0001 | g0081 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0148 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02723 | hp1 | a0001 | c0003 | t0002 | g0256 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02723 | hp2 | a0001 | c0006 | t0001 | g0142 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0147 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02818 | hp2 | a0001 | c0004 | t0001 | g0028 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0155 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02897 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0149 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02922 | hp2 | a0001 | c0008 | t0002 | g0259 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02970 | hp1 | a0001 | c0006 | t0001 | g0144 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0286 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03041 | hp1 | a0001 | c0006 | t0001 | g0034 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03098 | hp1 | a0002 | c0005 | t0003 | g0039 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03195 | hp1 | a0002 | c0005 | t0003 | g0159 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0037 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03225 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0068 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03239 | hp1 | a0001 | c0001 | t0008 | g0255 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0309 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0154 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03491 | hp2 | a0003 | c0010 | t0001 | g0246 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03492 | hp2 | a0003 | c0010 | t0001 | g0245 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0064 | AFR | ESN | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03579 | hp1 | a0002 | c0005 | t0003 | g0061 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0298 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0261 | SAS | BEB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0296 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG04204 | hp1 | a0002 | c0005 | t0003 | g0116 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0278 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG04228 | hp2 | a0001 | c0002 | t0006 | g0290 | SAS | STU | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18522 | hp1 | a0001 | c0015 | t0001 | g0062 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18939 | hp2 | a0001 | c0019 | t0001 | g0213 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18941 | hp1 | a0001 | c0004 | t0001 | g0129 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18941 | hp2 | a0009 | c0014 | t0001 | g0098 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18942 | hp2 | a0002 | c0005 | t0003 | g0113 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18945 | hp2 | a0002 | c0005 | t0003 | g0135 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18948 | hp1 | a0001 | c0003 | t0004 | g0053 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18949 | hp1 | a0001 | c0007 | t0001 | g0124 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18950 | hp2 | a0001 | c0004 | t0001 | g0031 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18952 | hp1 | a0001 | c0007 | t0001 | g0130 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18952 | hp2 | a0001 | c0004 | t0001 | g0177 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18957 | hp2 | a0001 | c0003 | t0004 | g0052 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18959 | hp2 | a0002 | c0005 | t0003 | g0241 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18960 | hp1 | a0007 | c0017 | t0001 | g0226 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18961 | hp2 | a0001 | c0002 | t0007 | g0307 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18962 | hp2 | a0001 | c0004 | t0001 | g0176 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18968 | hp2 | a0004 | c0012 | t0001 | g0219 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0302 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18971 | hp2 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18973 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18974 | hp2 | a0001 | c0002 | t0007 | g0308 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18975 | hp2 | a0001 | c0004 | t0001 | g0090 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18977 | hp2 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18978 | hp1 | a0001 | c0007 | t0001 | g0108 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18981 | hp1 | a0001 | c0004 | t0001 | g0020 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18998 | hp2 | a0002 | c0005 | t0003 | g0120 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18999 | hp1 | a0001 | c0007 | t0001 | g0015 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19000 | hp1 | a0002 | c0005 | t0003 | g0036 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19002 | hp1 | a0001 | c0003 | t0004 | g0057 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19005 | hp1 | a0008 | c0018 | t0001 | g0023 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19010 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19010 | hp2 | a0001 | c0007 | t0001 | g0127 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19012 | hp2 | a0002 | c0005 | t0003 | g0121 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0163 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19058 | hp1 | a0001 | c0004 | t0001 | g0091 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19062 | hp1 | a0001 | c0006 | t0001 | g0049 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19063 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19076 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19079 | hp1 | a0001 | c0003 | t0004 | g0051 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19082 | hp1 | a0001 | c0003 | t0004 | g0050 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19086 | hp1 | a0001 | c0004 | t0001 | g0175 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19086 | hp2 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19087 | hp1 | a0001 | c0007 | t0001 | g0131 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19090 | hp2 | a0001 | c0004 | t0001 | g0103 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19240 | hp1 | a0001 | c0004 | t0001 | g0007 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA20129 | hp1 | a0001 | c0004 | t0001 | g0233 | AFR | ASW | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA20129 | hp2 | a0002 | c0005 | t0003 | g0160 | AFR | ASW | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA20752 | hp1 | a0001 | c0020 | t0001 | g0221 | EUR | TSI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | GIH | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | GIH | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0292 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02109 | hp2 | a0001 | c0008 | t0002 | g0260 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02486 | hp1 | a0001 | c0006 | t0009 | g0153 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0274 | AFR | ACB | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03471 | hp1 | a0001 | c0003 | t0003 | g0150 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0311 | AFR | MSL | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0065 | AFR | USA | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA18955 | hp2 | a0005 | c0016 | t0001 | g0085 | EAS | JPT | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | USA | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | USA | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0263 | AFR | LWK | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0184 | REF | REF | ALOX5_chr10_45369216_45451117 | ALOX5 | chr10 | 45369216 | 45451117 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:45374371
|
G | A | 1 | a0004 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.92G>A | p.Gly31Asp | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | 156/2519 | 92/2025 | 31/674 | chr10 | 45374371 | ||
chr10:45382625
|
T | A | 1 | a0009 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.293T>A | p.Phe98Tyr | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/14 | 357/2519 | 293/2025 | 98/674 | chr10 | 45382625 | ||
chr10:45425058
|
G | A | 1 | a0002 | 16 | HG01243.hp2 HG02040.hp1 HG02080.hp2 others(13): Show |
missense_variant | MODERATE | c.760G>A | p.Glu254Lys | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/14 | 824/2519 | 760/2025 | 254/674 | chr10 | 45425058 | ||
chr10:45440532
|
G | A | 1 | a0005 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1084G>A | p.Val362Ile | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/14 | 1148/2519 | 1084/2025 | 362/674 | chr10 | 45440532 | ||
chr10:45440559
|
C | T | 1 | a0006 | 1 | HG02258.hp2 | stop_gained | HIGH | c.1111C>T | p.Arg371* | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/14 | 1175/2519 | 1111/2025 | 371/674 | chr10 | 45440559 | ||
chr10:45443104
|
G | T | 1 | a0008 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.1339G>T | p.Ala447Ser | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 10/14 | 1403/2519 | 1339/2025 | 447/674 | chr10 | 45443104 | ||
chr10:45443652
|
ATCCGGGC others(79): Show |
A | 1 | a0007 | 1 | NA18960.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1574-73_1586delCGG others(83): Show |
p.Phe526fs | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 12/14 | 1574/2025 | 525/674 | INFO_REALIGN_3_PRIME | chr10 | 45443652 | ||
chr10:45445628
|
A | C | 1 | a0003 | 2 | HG03491.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.1966A>C | p.Lys656Gln | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 2030/2519 | 1966/2025 | 656/674 | chr10 | 45445628 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:45374300
|
C | T | 5 | a0001c0002a0001c0008a0001c0011others(2): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
synonymous_variant | LOW | c.21C>T | p.Thr7Thr | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | 85/2519 | 21/2025 | 7/674 | chr10 | 45374300 | ||
chr10:45382569
|
C | T | 1 | a0001c0020 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.237C>T | p.Asp79Asp | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/14 | 301/2519 | 237/2025 | 79/674 | chr10 | 45382569 | ||
chr10:45382602
|
G | A | 4 | a0001c0003a0001c0006a0001c0021others(1): Show | 45 | HG01099.hp1 HG01258.hp1 HG01261.hp2 others(42): Show |
synonymous_variant | LOW | c.270G>A | p.Thr90Thr | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/14 | 334/2519 | 270/2025 | 90/674 | chr10 | 45382602 | ||
chr10:45382650
|
C | T | 1 | a0001c0019 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.318C>T | p.Gly106Gly | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/14 | 382/2519 | 318/2025 | 106/674 | chr10 | 45382650 | ||
chr10:45425069
|
G | A | 1 | a0001c0022 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.771G>A | p.Pro257Pro | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/14 | 835/2519 | 771/2025 | 257/674 | chr10 | 45425069 | ||
chr10:45425078
|
G | A | 1 | a0001c0007 | 6 | NA18949.hp1 NA18952.hp1 NA18978.hp1 others(3): Show |
synonymous_variant | LOW | c.780G>A | p.Thr260Thr | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/14 | 844/2519 | 780/2025 | 260/674 | chr10 | 45425078 | ||
chr10:45440444
|
G | A | 2 | a0001c0011a0001c0015 | 3 | HG00741.hp2 HG01192.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.996G>A | p.Pro332Pro | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/14 | 1060/2519 | 996/2025 | 332/674 | chr10 | 45440444 | ||
chr10:45443061
|
G | C | 1 | a0001c0009 | 2 | HG02572.hp1 HG02717.hp1 |
synonymous_variant | LOW | c.1296G>C | p.Gly432Gly | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 10/14 | 1360/2519 | 1296/2025 | 432/674 | chr10 | 45443061 | ||
chr10:45444169
|
A | G | 4 | a0001c0004a0001c0006a0001c0008others(1): Show | 43 | HG00280.hp2 HG00408.hp1 HG01109.hp1 others(40): Show |
synonymous_variant | LOW | c.1728A>G | p.Pro576Pro | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/14 | 1792/2519 | 1728/2025 | 576/674 | chr10 | 45444169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:45374221
|
C | T | 9 | a0001c0001t0002a0001c0002t0002a0001c0002t0006others(6): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
5_prime_UTR_variant | MODIFIER | c.-59C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | 59 | chr10 | 45374221 | |||||
chr10:45374252
|
G | C | 9 | a0001c0001t0002a0001c0002t0002a0001c0002t0006others(6): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
5_prime_UTR_variant | MODIFIER | c.-28G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | 28 | chr10 | 45374252 | |||||
chr10:45374265
|
C | G | 9 | a0001c0001t0002a0001c0002t0002a0001c0002t0006others(6): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-15C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | chr10 | 45374265 | ||||||
chr10:45374267
|
C | A | 2 | a0001c0002t0006a0001c0021t0006 | 2 | HG02698.hp1 HG04228.hp2 |
5_prime_UTR_variant | MODIFIER | c.-13C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/14 | 13 | chr10 | 45374267 | |||||
chr10:45445702
|
TCA | T | 3 | a0001c0001t0004a0001c0002t0007a0001c0003t0004 | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*17_*18delAC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 17 | INFO_REALIGN_3_PRIME | chr10 | 45445702 | ||||
chr10:45445758
|
T | C | 1 | a0001c0001t0008 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*71T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 71 | chr10 | 45445758 | |||||
chr10:45445957
|
C | T | 1 | a0001c0006t0009 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*270C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 270 | chr10 | 45445957 | |||||
chr10:45445963
|
C | A | 2 | a0001c0003t0003a0002c0005t0003 | 17 | HG01243.hp2 HG02040.hp1 HG02080.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*276C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 276 | chr10 | 45445963 | |||||
chr10:45446051
|
C | A | 1 | a0001c0001t0005 | 2 | HG01346.hp1 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*364C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 14/14 | 364 | chr10 | 45446051 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:45374447
|
A | G | 62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+18A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374447 | ||||||
chr10:45374455
|
A | G | 62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+26A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374455 | ||||||
chr10:45374470
|
G | A | 1 | a0001c0004t0001g0028 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.150+41G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374470 | ||||||
chr10:45374567
|
C | G | 1 | a0001c0002t0002g0313 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.150+138C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374567 | ||||||
chr10:45374572
|
A | C | 61 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(58): Show | 66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+143A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374572 | ||||||
chr10:45374693
|
T | G | 61 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(58): Show | 66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+264T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374693 | ||||||
chr10:45374857
|
T | G | 62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+428T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374857 | ||||||
chr10:45374858
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.150+429G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374858 | ||||||
chr10:45374890
|
G | A | 2 | a0001c0011t0002g0257a0001c0011t0002g0258 | 2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.150+461G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374890 | ||||||
chr10:45374999
|
G | A | 1 | a0001c0004t0001g0031 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.150+570G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45374999 | ||||||
chr10:45375077
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0008g0255 | 2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.150+648C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375077 | ||||||
chr10:45375095
|
C | G | 1 | a0006c0013t0001g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.150+666C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375095 | ||||||
chr10:45375113
|
T | G | 62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+684T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375113 | ||||||
chr10:45375162
|
T | C | 62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+733T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375162 | ||||||
chr10:45375240
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0019others(96): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.150+811C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375240 | ||||||
chr10:45375242
|
A | G | 62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+813A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375242 | ||||||
chr10:45375339
|
T | A | 6 | a0001c0001t0001g0035a0001c0003t0001g0006a0001c0003t0001g0032others(3): Show | 8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+910T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375339 | ||||||
chr10:45375379
|
G | T | 1 | a0001c0003t0002g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+950G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375379 | ||||||
chr10:45375436
|
G | A | 1 | a0001c0003t0002g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+1007G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375436 | ||||||
chr10:45375537
|
G | C | 1 | a0001c0004t0001g0168 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.150+1108G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375537 | ||||||
chr10:45375541
|
A | C | 1 | a0001c0001t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.150+1112A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375541 | ||||||
chr10:45375710
|
C | CT | 62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1281_150+1282i others(3): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375710 | ||||||
chr10:45375731
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.150+1302A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375731 | ||||||
chr10:45375775
|
C | T | 1 | a0001c0008t0002g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150+1346C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375775 | ||||||
chr10:45375881
|
G | A | 62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1452G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375881 | ||||||
chr10:45375903
|
C | T | 1 | a0001c0003t0002g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+1474C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375903 | ||||||
chr10:45375984
|
G | A | 62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1555G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45375984 | ||||||
chr10:45376106
|
T | C | 62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1677T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376106 | ||||||
chr10:45376190
|
T | TCTTCCCC others(4): Show |
62 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(59): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1762_150+1763i others(13): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 45376190 | |||||
chr10:45376192
|
G | T | 63 | a0001c0001t0001g0251a0001c0001t0002g0305a0001c0001t0002g0306others(60): Show | 68 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.150+1763G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376192 | ||||||
chr10:45376217
|
G | A | 1 | a0001c0003t0002g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+1788G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376217 | ||||||
chr10:45376263
|
G | A | 1 | a0001c0003t0002g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+1834G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376263 | ||||||
chr10:45376333
|
G | A | 1 | a0002c0005t0003g0036 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.150+1904G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376333 | ||||||
chr10:45376435
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.150+2006A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376435 | ||||||
chr10:45376469
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.150+2040A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376469 | ||||||
chr10:45376695
|
C | T | 3 | a0001c0002t0002g0309a0001c0002t0002g0310a0001c0002t0002g0311 | 3 | HG01243.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.150+2266C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376695 | ||||||
chr10:45376762
|
T | A | 61 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(58): Show | 66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+2333T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376762 | ||||||
chr10:45376768
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.150+2339G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376768 | ||||||
chr10:45376833
|
G | A | 61 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(58): Show | 66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+2404G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376833 | ||||||
chr10:45376904
|
C | A | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.150+2475C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376904 | ||||||
chr10:45376907
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.150+2478A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376907 | ||||||
chr10:45376910
|
C | G | 2 | a0001c0002t0007g0307a0001c0002t0007g0308 | 2 | NA18961.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.150+2481C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45376910 | ||||||
chr10:45377124
|
C | T | 6 | a0001c0001t0001g0035a0001c0003t0001g0006a0001c0003t0001g0032others(3): Show | 8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+2695C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377124 | ||||||
chr10:45377185
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.150+2756A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377185 | ||||||
chr10:45377246
|
A | T | 1 | a0001c0003t0001g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.150+2817A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377246 | ||||||
chr10:45377416
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0019others(96): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.150+2987C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377416 | ||||||
chr10:45377436
|
T | C | 1 | a0001c0004t0001g0037 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.150+3007T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377436 | ||||||
chr10:45377506
|
C | T | 61 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(58): Show | 66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.150+3077C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377506 | ||||||
chr10:45377519
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.150+3090A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377519 | ||||||
chr10:45377657
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.150+3228C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377657 | ||||||
chr10:45377744
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.150+3315C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377744 | ||||||
chr10:45377748
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.150+3319C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377748 | ||||||
chr10:45377830
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.150+3401A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377830 | ||||||
chr10:45377958
|
G | C | 1 | a0001c0003t0002g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+3529G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45377958 | ||||||
chr10:45378054
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.150+3625C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45378054 | ||||||
chr10:45378181
|
C | CT | 58 | a0001c0001t0002g0305a0001c0002t0002g0004a0001c0002t0002g0025others(55): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.150+3754dupT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 45378181 | |||||
chr10:45378253
|
AG | A | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+3827delG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 45378253 | |||||
chr10:45378673
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.151-3810G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45378673 | ||||||
chr10:45378881
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.151-3602G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45378881 | ||||||
chr10:45378892
|
T | C | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-3591T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45378892 | ||||||
chr10:45379062
|
C | T | 2 | a0001c0008t0002g0259a0001c0008t0002g0260 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.151-3421C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379062 | ||||||
chr10:45379120
|
G | A | 2 | a0001c0001t0001g0171a0001c0004t0001g0038 | 2 | HG00280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.151-3363G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379120 | ||||||
chr10:45379212
|
A | G | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-3271A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379212 | ||||||
chr10:45379356
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.151-3127G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379356 | ||||||
chr10:45379369
|
G | T | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-3114G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379369 | ||||||
chr10:45379370
|
C | T | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-3113C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379370 | ||||||
chr10:45379385
|
C | T | 4 | a0001c0001t0001g0157a0002c0005t0003g0158a0002c0005t0003g0159others(1): Show | 4 | HG02647.hp2 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-3098C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379385 | ||||||
chr10:45379452
|
C | T | 2 | a0001c0008t0002g0259a0001c0008t0002g0260 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.151-3031C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379452 | ||||||
chr10:45379614
|
G | A | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-2869G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379614 | ||||||
chr10:45379618
|
T | C | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-2865T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379618 | ||||||
chr10:45379643
|
T | C | 6 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0003t0001g0174others(3): Show | 6 | HG01258.hp1 HG01358.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-2840T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379643 | ||||||
chr10:45379647
|
T | A | 6 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0003t0001g0174others(3): Show | 6 | HG01258.hp1 HG01358.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-2836T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379647 | ||||||
chr10:45379684
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151-2799C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379684 | ||||||
chr10:45379685
|
G | A | 5 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0033others(2): Show | 7 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-2798G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379685 | ||||||
chr10:45379816
|
C | G | 7 | a0001c0002t0002g0299a0001c0002t0002g0300a0001c0002t0002g0301others(4): Show | 7 | HG00408.hp2 NA18942.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-2667C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379816 | ||||||
chr10:45379882
|
G | C | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-2601G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379882 | ||||||
chr10:45379924
|
G | C | 1 | a0001c0001t0005g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.151-2559G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379924 | ||||||
chr10:45379961
|
A | G | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-2522A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45379961 | ||||||
chr10:45380106
|
C | T | 8 | a0001c0002t0002g0027a0001c0002t0002g0292a0001c0002t0002g0293others(5): Show | 9 | HG00099.hp1 HG00323.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-2377C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380106 | ||||||
chr10:45380180
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.151-2303G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380180 | ||||||
chr10:45380345
|
T | C | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-2138T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380345 | ||||||
chr10:45380370
|
G | A | 1 | a0001c0002t0002g0261 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.151-2113G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380370 | ||||||
chr10:45380387
|
G | A | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.151-2096G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380387 | ||||||
chr10:45380485
|
C | T | 2 | a0003c0010t0001g0245a0003c0010t0001g0246 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.151-1998C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380485 | ||||||
chr10:45380532
|
C | T | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-1951C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380532 | ||||||
chr10:45380553
|
A | T | 1 | a0001c0001t0001g0244 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.151-1930A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380553 | ||||||
chr10:45380561
|
C | T | 2 | a0001c0008t0002g0259a0001c0008t0002g0260 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.151-1922C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380561 | ||||||
chr10:45380901
|
C | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.151-1582C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380901 | ||||||
chr10:45380933
|
C | T | 1 | a0002c0005t0003g0156 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.151-1550C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380933 | ||||||
chr10:45380937
|
A | G | 7 | a0001c0002t0002g0027a0001c0002t0002g0293a0001c0002t0002g0294others(4): Show | 8 | HG00099.hp1 HG00323.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-1546A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380937 | ||||||
chr10:45380974
|
G | A | 1 | a0001c0002t0002g0262 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.151-1509G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45380974 | ||||||
chr10:45381159
|
C | T | 57 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(54): Show | 62 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.151-1324C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381159 | ||||||
chr10:45381225
|
T | C | 65 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0305others(62): Show | 70 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.151-1258T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381225 | ||||||
chr10:45381329
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0002g0305 | 2 | HG01175.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.151-1154C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381329 | ||||||
chr10:45381335
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.151-1148G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381335 | ||||||
chr10:45381468
|
C | T | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-1015C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381468 | ||||||
chr10:45381492
|
G | T | 1 | a0001c0001t0001g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.151-991G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381492 | ||||||
chr10:45381558
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.151-925G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381558 | ||||||
chr10:45381669
|
A | G | 1 | a0002c0005t0003g0241 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.151-814A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381669 | ||||||
chr10:45381709
|
G | A | 59 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.151-774G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381709 | ||||||
chr10:45381711
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.151-772G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381711 | ||||||
chr10:45381856
|
G | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(312): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.151-627G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381856 | ||||||
chr10:45381993
|
C | A | 58 | a0001c0001t0002g0305a0001c0002t0002g0004a0001c0002t0002g0025others(55): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.151-490C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45381993 | ||||||
chr10:45382035
|
C | T | 2 | a0001c0008t0002g0259a0001c0008t0002g0260 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.151-448C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382035 | ||||||
chr10:45382112
|
G | A | 58 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(55): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.151-371G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382112 | ||||||
chr10:45382170
|
G | A | 1 | a0001c0002t0002g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.151-313G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382170 | ||||||
chr10:45382195
|
A | T | 25 | a0001c0003t0001g0006a0001c0003t0001g0016a0001c0003t0001g0017others(22): Show | 30 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.151-288A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382195 | ||||||
chr10:45382217
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.151-266T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382217 | ||||||
chr10:45382392
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151-91G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382392 | ||||||
chr10:45382451
|
C | T | 57 | a0001c0001t0002g0305a0001c0002t0002g0004a0001c0002t0002g0025others(54): Show | 62 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.151-32C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 1/13 | chr10 | 45382451 | ||||||
chr10:45382725
|
G | A | 13 | a0001c0003t0001g0055a0001c0003t0001g0056a0001c0003t0001g0058others(10): Show | 13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.349+44G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382725 | ||||||
chr10:45382810
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.349+129T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382810 | ||||||
chr10:45382818
|
G | A | 14 | a0001c0001t0001g0060a0001c0003t0001g0055a0001c0003t0001g0056others(11): Show | 14 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.349+137G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382818 | ||||||
chr10:45382865
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+184C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382865 | ||||||
chr10:45382933
|
G | A | 1 | a0001c0008t0002g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349+252G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382933 | ||||||
chr10:45382934
|
G | A | 93 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(90): Show | 105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.349+253G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382934 | ||||||
chr10:45382935
|
G | T | 1 | a0001c0002t0002g0304 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.349+254G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382935 | ||||||
chr10:45382938
|
G | T | 1 | a0001c0002t0002g0304 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.349+257G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45382938 | ||||||
chr10:45383015
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.349+334G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383015 | ||||||
chr10:45383023
|
C | G | 1 | a0001c0001t0001g0240 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.349+342C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383023 | ||||||
chr10:45383229
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0164a0001c0001t0001g0165others(6): Show | 12 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+548G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383229 | ||||||
chr10:45383351
|
C | T | 5 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0033others(2): Show | 7 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+670C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383351 | ||||||
chr10:45383352
|
G | A | 12 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(9): Show | 13 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.349+671G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383352 | ||||||
chr10:45383444
|
C | G | 3 | a0001c0001t0002g0306a0001c0008t0002g0259a0001c0008t0002g0260 | 3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.349+763C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383444 | ||||||
chr10:45383450
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+769A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383450 | ||||||
chr10:45383460
|
A | G | 61 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(58): Show | 66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.349+779A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383460 | ||||||
chr10:45383610
|
G | T | 2 | a0001c0004t0001g0008a0001c0004t0001g0068 | 3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.349+929G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383610 | ||||||
chr10:45383612
|
G | A | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+931G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383612 | ||||||
chr10:45383614
|
G | A | 35 | a0001c0002t0002g0025a0001c0002t0002g0026a0001c0002t0002g0261others(32): Show | 37 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.349+933G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383614 | ||||||
chr10:45383636
|
T | C | 1 | a0001c0008t0002g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349+955T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383636 | ||||||
chr10:45383841
|
C | T | 1 | a0001c0003t0004g0057 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.349+1160C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45383841 | ||||||
chr10:45384018
|
A | G | 1 | a0001c0002t0002g0284 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.349+1337A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384018 | ||||||
chr10:45384143
|
G | C | 1 | a0001c0002t0002g0264 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.349+1462G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384143 | ||||||
chr10:45384158
|
C | T | 14 | a0001c0001t0001g0139a0001c0003t0001g0055a0001c0003t0001g0056others(11): Show | 14 | HG01255.hp1 HG01261.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+1477C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384158 | ||||||
chr10:45384540
|
C | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG01361.hp1 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.349+1859C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384540 | ||||||
chr10:45384571
|
C | A | 1 | a0001c0003t0004g0047 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.349+1890C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384571 | ||||||
chr10:45384608
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(255): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.349+1927C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384608 | ||||||
chr10:45384616
|
C | G | 3 | a0001c0001t0002g0306a0001c0008t0002g0259a0001c0008t0002g0260 | 3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.349+1935C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384616 | ||||||
chr10:45384776
|
G | A | 1 | a0001c0002t0006g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.349+2095G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384776 | ||||||
chr10:45384833
|
C | CTAT | 6 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(3): Show | 7 | HG01069.hp1 HG02109.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+2175_349+2177d others(5): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45384833 | |||||
chr10:45384833
|
C | CTATTAT | 5 | a0001c0001t0001g0069a0001c0004t0001g0037a0001c0004t0001g0038others(2): Show | 5 | HG01243.hp2 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+2172_349+2177d others(8): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45384833 | |||||
chr10:45384833
|
C | CTATTATT others(5): Show |
14 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(11): Show | 15 | HG00099.hp1 HG00642.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.349+2166_349+2177d others(14): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45384833 | |||||
chr10:45384833
|
C | CTATTATT others(8): Show |
2 | a0001c0001t0001g0181a0001c0002t0002g0293 | 2 | HG00323.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.349+2163_349+2177d others(17): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45384833 | |||||
chr10:45384833
|
C | CTATTATT others(14): Show |
1 | a0001c0008t0002g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349+2157_349+2177d others(23): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45384833 | |||||
chr10:45384912
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+2231A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384912 | ||||||
chr10:45384918
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG00438.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.349+2237C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45384918 | ||||||
chr10:45385176
|
A | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+2495A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385176 | ||||||
chr10:45385210
|
G | A | 15 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0141others(12): Show | 17 | HG01099.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.349+2529G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385210 | ||||||
chr10:45385220
|
C | G | 15 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0141others(12): Show | 17 | HG01099.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.349+2539C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385220 | ||||||
chr10:45385306
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+2625G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385306 | ||||||
chr10:45385530
|
G | A | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+2849G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385530 | ||||||
chr10:45385966
|
G | T | 1 | a0001c0002t0002g0027 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.349+3285G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385966 | ||||||
chr10:45385991
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.349+3310C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45385991 | ||||||
chr10:45386066
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.349+3385C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386066 | ||||||
chr10:45386073
|
G | A | 4 | a0001c0001t0002g0305a0001c0003t0001g0154a0001c0003t0001g0163others(1): Show | 4 | HG02486.hp1 HG02615.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+3392G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386073 | ||||||
chr10:45386097
|
C | G | 1 | a0001c0002t0002g0293 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.349+3416C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386097 | ||||||
chr10:45386230
|
A | G | 70 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(67): Show | 75 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.349+3549A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386230 | ||||||
chr10:45386300
|
CA | C | 28 | a0001c0001t0001g0043a0001c0002t0002g0303a0001c0003t0001g0006others(25): Show | 33 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.349+3635delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45386300 | |||||
chr10:45386467
|
TA | T | 7 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(4): Show | 7 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+3794delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45386467 | |||||
chr10:45386582
|
G | GA | 8 | a0001c0001t0001g0070a0001c0001t0001g0164a0001c0001t0001g0165others(5): Show | 8 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+3910dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45386582 | |||||
chr10:45386626
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.349+3945T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386626 | ||||||
chr10:45386670
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.349+3989A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386670 | ||||||
chr10:45386710
|
C | T | 5 | a0001c0001t0001g0060a0002c0005t0003g0061a0002c0005t0003g0158others(2): Show | 5 | HG02647.hp2 HG03195.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+4029C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45386710 | ||||||
chr10:45387055
|
G | A | 2 | a0001c0004t0001g0037a0001c0004t0001g0038 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.349+4374G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387055 | ||||||
chr10:45387115
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+4434G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387115 | ||||||
chr10:45387144
|
A | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+4463A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387144 | ||||||
chr10:45387293
|
A | G | 70 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(67): Show | 75 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.349+4612A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387293 | ||||||
chr10:45387374
|
G | A | 1 | a0001c0002t0007g0307 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.349+4693G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387374 | ||||||
chr10:45387412
|
G | A | 3 | a0001c0003t0001g0154a0001c0003t0001g0163a0001c0006t0009g0153 | 3 | HG02486.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.349+4731G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387412 | ||||||
chr10:45387498
|
C | CTTTCTCC others(67): Show |
1 | a0001c0001t0001g0105 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.349+4818_349+4891d others(76): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45387498 | |||||
chr10:45387516
|
A | C | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.349+4835A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387516 | ||||||
chr10:45387568
|
A | G | 1 | a0001c0003t0002g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.349+4887A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387568 | ||||||
chr10:45387618
|
G | C | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.349+4937G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387618 | ||||||
chr10:45387630
|
C | T | 1 | a0002c0005t0003g0135 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.349+4949C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387630 | ||||||
chr10:45387643
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.349+4962G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387643 | ||||||
chr10:45387858
|
A | G | 2 | a0001c0011t0002g0257a0001c0011t0002g0258 | 2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.349+5177A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387858 | ||||||
chr10:45387958
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(255): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.349+5277A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387958 | ||||||
chr10:45387972
|
C | G | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.349+5291C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45387972 | ||||||
chr10:45388023
|
T | A | 17 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.349+5342T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388023 | ||||||
chr10:45388088
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.349+5407A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388088 | ||||||
chr10:45388144
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+5463T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388144 | ||||||
chr10:45388277
|
G | A | 7 | a0001c0001t0001g0136a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+5596G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388277 | ||||||
chr10:45388326
|
AG | A | 17 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.349+5646delG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388326 | ||||||
chr10:45388570
|
G | A | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+5889G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388570 | ||||||
chr10:45388671
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.349+5990A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388671 | ||||||
chr10:45388687
|
A | G | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+6006A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388687 | ||||||
chr10:45388777
|
C | A | 13 | a0001c0003t0001g0055a0001c0003t0001g0056a0001c0003t0001g0058others(10): Show | 13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.349+6096C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388777 | ||||||
chr10:45388814
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.349+6133C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388814 | ||||||
chr10:45388835
|
G | A | 1 | a0002c0005t0003g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.349+6154G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388835 | ||||||
chr10:45388885
|
A | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0106a0001c0001t0001g0107 | 4 | HG01069.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+6204A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45388885 | ||||||
chr10:45388923
|
C | CA | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+6249dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45388923 | |||||
chr10:45389034
|
T | C | 1 | a0006c0013t0001g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.349+6353T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389034 | ||||||
chr10:45389063
|
C | T | 1 | a0002c0005t0003g0135 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.349+6382C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389063 | ||||||
chr10:45389069
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0072 | 2 | HG01123.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.349+6388G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389069 | ||||||
chr10:45389123
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+6442C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389123 | ||||||
chr10:45389158
|
A | T | 7 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(4): Show | 9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.349+6477A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389158 | ||||||
chr10:45389283
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.350-6572A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389283 | ||||||
chr10:45389443
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.350-6412G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389443 | ||||||
chr10:45389458
|
C | G | 8 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-6397C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389458 | ||||||
chr10:45389506
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-6349C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389506 | ||||||
chr10:45389546
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-6309C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389546 | ||||||
chr10:45389721
|
ACCAG | A | 43 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(40): Show | 47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-6130_350-6127d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45389721 | |||||
chr10:45389793
|
C | T | 1 | a0001c0004t0001g0103 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.350-6062C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389793 | ||||||
chr10:45389807
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.350-6048A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389807 | ||||||
chr10:45389813
|
G | A | 1 | a0001c0002t0002g0309 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.350-6042G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389813 | ||||||
chr10:45389872
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0043 | 3 | HG01070.hp1 HG01071.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.350-5983T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389872 | ||||||
chr10:45389873
|
GCTCCAAT others(29): Show |
G | 1 | a0001c0001t0001g0236 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.350-5981_350-5946d others(38): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389873 | ||||||
chr10:45389878
|
A | T | 1 | a0001c0002t0002g0289 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.350-5977A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389878 | ||||||
chr10:45389959
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.350-5896C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389959 | ||||||
chr10:45389960
|
G | A | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-5895G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389960 | ||||||
chr10:45389973
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-5882A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45389973 | ||||||
chr10:45390029
|
G | C | 17 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.350-5826G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390029 | ||||||
chr10:45390151
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0101others(1): Show | 6 | HG00621.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-5704C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390151 | ||||||
chr10:45390226
|
C | T | 1 | a0001c0008t0002g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.350-5629C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390226 | ||||||
chr10:45390364
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-5491C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390364 | ||||||
chr10:45390418
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-5437T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390418 | ||||||
chr10:45390483
|
C | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(4): Show | 8 | HG01069.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-5372C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390483 | ||||||
chr10:45390581
|
C | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-5274C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390581 | ||||||
chr10:45390602
|
A | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-5253A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390602 | ||||||
chr10:45390605
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.350-5250G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390605 | ||||||
chr10:45390834
|
T | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(7): Show | 12 | HG02258.hp1 HG02809.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.350-5021T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390834 | ||||||
chr10:45390846
|
C | G | 7 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(4): Show | 9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-5009C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390846 | ||||||
chr10:45390847
|
A | G | 43 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(40): Show | 47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-5008A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45390847 | ||||||
chr10:45390988
|
CCCCTCT | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0235others(1): Show | 4 | HG01106.hp1 HG03669.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-4863_350-4858d others(8): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45390988 | |||||
chr10:45390998
|
CTCTCCCC others(35): Show |
C | 2 | a0001c0002t0002g0266a0001c0002t0002g0267 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.350-4845_350-4804d others(44): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45390998 | |||||
chr10:45391002
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.350-4853C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391002 | ||||||
chr10:45391003
|
CCCTCTCT | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(180): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.350-4845_350-4839d others(9): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391003 | |||||
chr10:45391009
|
CT | C | 9 | a0001c0001t0002g0306a0001c0002t0002g0280a0001c0002t0002g0281others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-4845delT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391009 | ||||||
chr10:45391010
|
T | C | 78 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0060others(75): Show | 83 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.350-4845T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391010 | ||||||
chr10:45391012
|
C | A | 18 | a0001c0001t0001g0231a0001c0003t0001g0055a0001c0003t0001g0056others(15): Show | 18 | HG01243.hp2 HG01256.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.350-4843C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391012 | ||||||
chr10:45391015
|
TCCCATCT others(8): Show |
T | 1 | a0001c0009t0001g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.350-4836_350-4822d others(17): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391015 | |||||
chr10:45391018
|
CA | C | 44 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0002t0002g0004others(41): Show | 48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.350-4836delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391018 | ||||||
chr10:45391019
|
A | C | 9 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0002t0002g0309others(6): Show | 10 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-4836A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391019 | ||||||
chr10:45391022
|
TC | T | 35 | a0001c0001t0002g0305a0001c0002t0002g0004a0001c0002t0002g0025others(32): Show | 39 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.350-4829delC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391022 | |||||
chr10:45391025
|
CCTCTCCC others(23): Show |
C | 9 | a0001c0001t0002g0306a0001c0002t0002g0280a0001c0002t0002g0281others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-4826_350-4797d others(32): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391025 | |||||
chr10:45391026
|
C | A | 4 | a0001c0004t0001g0007a0001c0004t0001g0064a0001c0004t0001g0065others(1): Show | 5 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-4829C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391026 | ||||||
chr10:45391030
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.350-4825C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391030 | ||||||
chr10:45391032
|
CCTCTCCC others(16): Show |
C | 35 | a0001c0001t0002g0305a0001c0002t0002g0004a0001c0002t0002g0025others(32): Show | 39 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.350-4819_350-4797d others(25): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391032 | |||||
chr10:45391039
|
CA | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(5): Show | 9 | HG02572.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-4815delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391039 | ||||||
chr10:45391040
|
A | C | 4 | a0001c0004t0001g0007a0001c0004t0001g0064a0001c0004t0001g0065others(1): Show | 5 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-4815A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391040 | ||||||
chr10:45391043
|
TC | T | 12 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(9): Show | 14 | HG02258.hp1 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-4808delC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391043 | |||||
chr10:45391046
|
C | G | 22 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(19): Show | 23 | HG01069.hp1 HG02071.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-4809C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391046 | ||||||
chr10:45391050
|
TC | T | 4 | a0001c0004t0001g0007a0001c0004t0001g0064a0001c0004t0001g0065others(1): Show | 5 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-4801delC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391050 | |||||
chr10:45391053
|
CCT | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(5): Show | 9 | HG02572.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-4798_350-4797d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391053 | |||||
chr10:45391057
|
T | A | 52 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(49): Show | 57 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.350-4798T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391057 | ||||||
chr10:45391059
|
C | G | 52 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(49): Show | 57 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.350-4796C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391059 | ||||||
chr10:45391060
|
C | CCACGG | 4 | a0001c0004t0001g0007a0001c0004t0001g0064a0001c0004t0001g0065others(1): Show | 5 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-4795_350-4794i others(7): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391060 | ||||||
chr10:45391060
|
C | G | 52 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(49): Show | 57 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.350-4795C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391060 | ||||||
chr10:45391072
|
CCACGG | C | 56 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(53): Show | 62 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.350-4782_350-4778d others(7): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391072 | ||||||
chr10:45391077
|
G | GTCTCCC | 7 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0001g0189others(4): Show | 7 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-4765_350-4760d others(8): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391077 | |||||
chr10:45391077
|
G | GTCTCCCT others(5): Show |
187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(184): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.350-4771_350-4760d others(14): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391077 | |||||
chr10:45391077
|
G | GTCTCCCT others(40): Show |
1 | a0001c0001t0001g0236 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.350-4760_350-4759i others(49): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391077 | |||||
chr10:45391081
|
C | CCCTCTCC others(5): Show |
6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-4763_350-4762i others(14): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391081 | |||||
chr10:45391092
|
T | TCCCTCTC others(6): Show |
1 | a0001c0007t0001g0108 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.350-4760_350-4759i others(15): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391092 | |||||
chr10:45391106
|
C | A | 1 | a0002c0005t0003g0241 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.350-4749C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391106 | ||||||
chr10:45391218
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.350-4637G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391218 | ||||||
chr10:45391240
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.350-4615G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391240 | ||||||
chr10:45391245
|
G | A | 1 | a0001c0003t0001g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.350-4610G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391245 | ||||||
chr10:45391256
|
CTG | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0179a0001c0001t0001g0180 | 6 | NA18944.hp2 NA18947.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-4597_350-4596d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391256 | |||||
chr10:45391326
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.350-4529C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391326 | ||||||
chr10:45391329
|
G | A | 43 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(40): Show | 47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-4526G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391329 | ||||||
chr10:45391425
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.350-4430C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391425 | ||||||
chr10:45391438
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.350-4417C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391438 | ||||||
chr10:45391508
|
C | T | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(10): Show | 14 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-4347C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391508 | ||||||
chr10:45391513
|
A | AC | 21 | a0001c0001t0001g0041a0001c0001t0001g0066a0001c0001t0001g0079others(18): Show | 21 | HG00621.hp1 HG00642.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.350-4338dupC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391513 | |||||
chr10:45391538
|
C | T | 1 | a0001c0003t0001g0018 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.350-4317C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391538 | ||||||
chr10:45391550
|
A | G | 7 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(4): Show | 7 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-4305A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391550 | ||||||
chr10:45391557
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0008g0255 | 2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.350-4298G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391557 | ||||||
chr10:45391568
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-4287A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391568 | ||||||
chr10:45391580
|
T | C | 2 | a0001c0008t0002g0259a0001c0008t0002g0260 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.350-4275T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391580 | ||||||
chr10:45391587
|
C | A | 43 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(40): Show | 47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-4268C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391587 | ||||||
chr10:45391612
|
G | A | 2 | a0001c0001t0001g0194a0001c0003t0004g0047 | 2 | HG00140.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.350-4243G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391612 | ||||||
chr10:45391622
|
G | A | 43 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(40): Show | 47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-4233G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391622 | ||||||
chr10:45391667
|
C | T | 17 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.350-4188C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391667 | ||||||
chr10:45391670
|
A | G | 17 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.350-4185A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391670 | ||||||
chr10:45391671
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.350-4184T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391671 | ||||||
chr10:45391673
|
G | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0164a0001c0001t0001g0171others(6): Show | 10 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-4182G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391673 | ||||||
chr10:45391770
|
G | A | 1 | a0001c0007t0001g0124 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.350-4085G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391770 | ||||||
chr10:45391783
|
C | G | 1 | a0006c0013t0001g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.350-4072C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391783 | ||||||
chr10:45391783
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(132): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.350-4072C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391783 | ||||||
chr10:45391806
|
ACCCTCCG others(57): Show |
A | 1 | a0001c0001t0001g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.350-4026_350-3963d others(66): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391806 | |||||
chr10:45391808
|
C | T | 1 | a0002c0005t0003g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.350-4047C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391808 | ||||||
chr10:45391817
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.350-4038G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391817 | ||||||
chr10:45391824
|
G | A | 17 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.350-4031G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391824 | ||||||
chr10:45391829
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(250): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.350-4026A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391829 | ||||||
chr10:45391853
|
ATCTGAGA others(33): Show |
A | 19 | a0001c0001t0001g0083a0001c0001t0001g0133a0001c0001t0001g0181others(16): Show | 20 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.350-3962_350-3923d others(42): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391853 | |||||
chr10:45391877
|
G | A | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3978G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391877 | ||||||
chr10:45391893
|
T | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(237): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.350-3962T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391893 | ||||||
chr10:45391912
|
CCTCCGCC others(33): Show |
C | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.350-3927_350-3888d others(42): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391912 | |||||
chr10:45391920
|
C | G | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-3935C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391920 | ||||||
chr10:45391926
|
C | A | 16 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(13): Show | 17 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-3929C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391926 | ||||||
chr10:45391927
|
C | T | 1 | a0001c0008t0002g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.350-3928C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391927 | ||||||
chr10:45391928
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-3927G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391928 | ||||||
chr10:45391933
|
G | A | 1 | a0001c0002t0002g0310 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.350-3922G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391933 | ||||||
chr10:45391948
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.350-3907A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391948 | ||||||
chr10:45391951
|
G | A | 1 | a0001c0003t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.350-3904G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391951 | ||||||
chr10:45391957
|
G | A | 7 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(4): Show | 9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-3898G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45391957 | ||||||
chr10:45391996
|
GTCAGCCC others(38): Show |
G | 1 | a0001c0002t0002g0299 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.350-3826_350-3782d others(47): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45391996 | |||||
chr10:45392024
|
G | A | 1 | a0001c0004t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.350-3831G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392024 | ||||||
chr10:45392026
|
C | T | 1 | a0001c0004t0001g0031 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.350-3829C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392026 | ||||||
chr10:45392027
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(146): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.350-3828C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392027 | ||||||
chr10:45392040
|
G | C | 26 | a0001c0003t0001g0006a0001c0003t0001g0016a0001c0003t0001g0017others(23): Show | 31 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.350-3815G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392040 | ||||||
chr10:45392051
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3804C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392051 | ||||||
chr10:45392064
|
G | A | 69 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(66): Show | 74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.350-3791G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392064 | ||||||
chr10:45392064
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.350-3791G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392064 | ||||||
chr10:45392069
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(4): Show | 8 | HG01069.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-3786G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392069 | ||||||
chr10:45392074
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3781A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392074 | ||||||
chr10:45392083
|
T | A | 17 | a0001c0002t0002g0025a0001c0002t0002g0262a0001c0002t0002g0264others(14): Show | 18 | HG00408.hp2 HG02132.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.350-3772T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392083 | ||||||
chr10:45392112
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3743T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392112 | ||||||
chr10:45392122
|
G | A | 26 | a0001c0003t0001g0006a0001c0003t0001g0016a0001c0003t0001g0017others(23): Show | 31 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.350-3733G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392122 | ||||||
chr10:45392145
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3710T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392145 | ||||||
chr10:45392182
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3673T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392182 | ||||||
chr10:45392247
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3608T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392247 | ||||||
chr10:45392352
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.350-3503G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392352 | ||||||
chr10:45392416
|
C | G | 1 | a0001c0011t0002g0258 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.350-3439C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392416 | ||||||
chr10:45392470
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(255): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.350-3385A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392470 | ||||||
chr10:45392513
|
G | A | 10 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(7): Show | 12 | HG02258.hp1 HG02809.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.350-3342G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392513 | ||||||
chr10:45392517
|
C | G | 23 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(20): Show | 24 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.350-3338C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392517 | ||||||
chr10:45392571
|
G | A | 43 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(40): Show | 47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-3284G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392571 | ||||||
chr10:45392574
|
T | A | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.350-3281T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392574 | ||||||
chr10:45392578
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0002g0306 | 2 | HG00621.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.350-3277C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392578 | ||||||
chr10:45392617
|
G | C | 5 | a0001c0001t0001g0165a0001c0004t0001g0037a0001c0004t0001g0038others(2): Show | 5 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-3238G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392617 | ||||||
chr10:45392660
|
C | T | 44 | a0001c0001t0002g0305a0001c0002t0002g0004a0001c0002t0002g0025others(41): Show | 48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.350-3195C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392660 | ||||||
chr10:45392720
|
AAAAAAGA others(4): Show |
A | 1 | a0002c0005t0003g0241 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.350-3132_350-3122d others(13): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45392720 | |||||
chr10:45392746
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(146): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.350-3109C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392746 | ||||||
chr10:45392818
|
T | C | 1 | a0001c0002t0002g0292 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.350-3037T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392818 | ||||||
chr10:45392903
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.350-2952G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392903 | ||||||
chr10:45392955
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-2900T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45392955 | ||||||
chr10:45393008
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(185): Show | 210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.350-2847G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393008 | ||||||
chr10:45393015
|
A | C | 2 | a0001c0011t0002g0257a0001c0011t0002g0258 | 2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.350-2840A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393015 | ||||||
chr10:45393055
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-2800A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393055 | ||||||
chr10:45393145
|
AC | A | 2 | a0001c0003t0001g0016a0001c0006t0001g0142 | 3 | HG02572.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.350-2709delC | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393145 | ||||||
chr10:45393148
|
C | CA | 5 | a0001c0001t0001g0079a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG01109.hp1 HG01261.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-2699dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45393148 | |||||
chr10:45393150
|
A | C | 34 | a0001c0002t0002g0025a0001c0002t0002g0026a0001c0002t0002g0262others(31): Show | 36 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.350-2705A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393150 | ||||||
chr10:45393151
|
A | AC | 2 | a0001c0003t0001g0016a0001c0006t0001g0142 | 3 | HG02572.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.350-2704_350-2703i others(3): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393151 | ||||||
chr10:45393155
|
A | G | 2 | a0001c0003t0001g0016a0001c0006t0001g0142 | 3 | HG02572.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.350-2700A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393155 | ||||||
chr10:45393157
|
C | G | 2 | a0001c0003t0001g0016a0001c0006t0001g0142 | 3 | HG02572.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.350-2698C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393157 | ||||||
chr10:45393188
|
G | A | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-2667G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393188 | ||||||
chr10:45393279
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.350-2576G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393279 | ||||||
chr10:45393296
|
A | C | 3 | a0001c0001t0002g0306a0001c0008t0002g0259a0001c0008t0002g0260 | 3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.350-2559A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393296 | ||||||
chr10:45393321
|
T | C | 3 | a0001c0002t0002g0309a0001c0002t0002g0310a0001c0002t0002g0311 | 3 | HG01243.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.350-2534T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393321 | ||||||
chr10:45393343
|
A | T | 1 | a0001c0003t0001g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-2512A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393343 | ||||||
chr10:45393352
|
C | A | 1 | a0001c0003t0001g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-2503C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393352 | ||||||
chr10:45393447
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-2408C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393447 | ||||||
chr10:45393480
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-2375A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393480 | ||||||
chr10:45393488
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-2367A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393488 | ||||||
chr10:45393497
|
A | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-2358A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393497 | ||||||
chr10:45393505
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-2350T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393505 | ||||||
chr10:45393507
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.350-2348G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393507 | ||||||
chr10:45393572
|
C | G | 3 | a0001c0002t0002g0309a0001c0002t0002g0310a0001c0002t0002g0311 | 3 | HG01243.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.350-2283C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393572 | ||||||
chr10:45393599
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.350-2256G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393599 | ||||||
chr10:45393725
|
C | T | 20 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0018others(17): Show | 23 | HG01099.hp1 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-2130C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393725 | ||||||
chr10:45393794
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.350-2061A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393794 | ||||||
chr10:45393835
|
G | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-2020G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393835 | ||||||
chr10:45393861
|
A | T | 1 | a0002c0005t0003g0241 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.350-1994A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393861 | ||||||
chr10:45393882
|
A | G | 1 | a0001c0002t0002g0283 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.350-1973A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393882 | ||||||
chr10:45393894
|
A | G | 3 | a0001c0001t0002g0306a0001c0008t0002g0259a0001c0008t0002g0260 | 3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.350-1961A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393894 | ||||||
chr10:45393944
|
C | T | 43 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(40): Show | 47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-1911C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393944 | ||||||
chr10:45393980
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1875C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393980 | ||||||
chr10:45393997
|
G | C | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-1858G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45393997 | ||||||
chr10:45394091
|
T | A | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1764T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394091 | ||||||
chr10:45394136
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.350-1719C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394136 | ||||||
chr10:45394137
|
G | A | 3 | a0001c0001t0002g0306a0001c0008t0002g0259a0001c0008t0002g0260 | 3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.350-1718G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394137 | ||||||
chr10:45394346
|
C | A | 5 | a0001c0001t0001g0165a0001c0004t0001g0037a0001c0004t0001g0038others(2): Show | 5 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-1509C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394346 | ||||||
chr10:45394403
|
G | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1452G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394403 | ||||||
chr10:45394434
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1421C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394434 | ||||||
chr10:45394538
|
A | G | 70 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(67): Show | 75 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.350-1317A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394538 | ||||||
chr10:45394635
|
C | T | 5 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0033others(2): Show | 7 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-1220C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394635 | ||||||
chr10:45394674
|
C | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1181C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394674 | ||||||
chr10:45394736
|
A | G | 1 | a0001c0011t0002g0258 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.350-1119A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394736 | ||||||
chr10:45394763
|
AAAAC | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(4): Show | 8 | HG02809.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-1085_350-1082d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45394763 | |||||
chr10:45394826
|
G | A | 70 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(67): Show | 75 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.350-1029G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394826 | ||||||
chr10:45394846
|
C | A | 20 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0199others(17): Show | 23 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-1009C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394846 | ||||||
chr10:45394909
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-946C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394909 | ||||||
chr10:45394928
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.350-927A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394928 | ||||||
chr10:45394984
|
G | A | 70 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(67): Show | 75 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.350-871G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394984 | ||||||
chr10:45394997
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(255): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.350-858T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45394997 | ||||||
chr10:45395211
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.350-644G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395211 | ||||||
chr10:45395314
|
G | T | 44 | a0001c0001t0002g0305a0001c0002t0002g0004a0001c0002t0002g0025others(41): Show | 48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.350-541G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395314 | ||||||
chr10:45395350
|
G | T | 42 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(39): Show | 46 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.350-505G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395350 | ||||||
chr10:45395373
|
A | G | 43 | a0001c0001t0002g0305a0001c0002t0002g0004a0001c0002t0002g0025others(40): Show | 47 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.350-482A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395373 | ||||||
chr10:45395389
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.350-466A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395389 | ||||||
chr10:45395476
|
G | C | 2 | a0002c0005t0003g0036a0002c0005t0003g0113 | 2 | NA18942.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.350-379G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395476 | ||||||
chr10:45395490
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.350-365A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395490 | ||||||
chr10:45395492
|
A | C | 1 | a0001c0009t0001g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.350-363A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395492 | ||||||
chr10:45395540
|
A | G | 70 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(67): Show | 75 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.350-315A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395540 | ||||||
chr10:45395546
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0179a0001c0001t0001g0180 | 6 | NA18944.hp2 NA18947.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-309G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395546 | ||||||
chr10:45395606
|
TA | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(254): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.350-236delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 45395606 | |||||
chr10:45395669
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.350-186G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395669 | ||||||
chr10:45395713
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0192a0001c0001t0001g0208others(2): Show | 6 | HG02132.hp1 NA18945.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-142G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395713 | ||||||
chr10:45395741
|
A | G | 25 | a0001c0003t0001g0006a0001c0003t0001g0016a0001c0003t0001g0017others(22): Show | 30 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.350-114A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395741 | ||||||
chr10:45395767
|
A | G | 13 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(10): Show | 14 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-88A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395767 | ||||||
chr10:45395778
|
G | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0232 | 2 | NA19070.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.350-77G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395778 | ||||||
chr10:45395805
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.350-50A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 2/13 | chr10 | 45395805 | ||||||
chr10:45395973
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+37A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45395973 | ||||||
chr10:45396018
|
C | T | 1 | a0001c0002t0002g0289 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.431+82C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396018 | ||||||
chr10:45396036
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(145): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.431+100A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396036 | ||||||
chr10:45396087
|
CA | C | 3 | a0001c0001t0002g0306a0001c0008t0002g0259a0001c0008t0002g0260 | 3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.431+154delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45396087 | |||||
chr10:45396115
|
CAA | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0166a0009c0014t0001g0098 | 3 | NA18941.hp2 NA18978.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.431+180_431+181del others(2): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396115 | ||||||
chr10:45396154
|
C | G | 1 | a0001c0004t0001g0028 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.431+218C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396154 | ||||||
chr10:45396162
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.431+226T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396162 | ||||||
chr10:45396252
|
T | C | 12 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(9): Show | 13 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+316T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396252 | ||||||
chr10:45396289
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+353T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396289 | ||||||
chr10:45396352
|
G | GA | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(255): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.431+420dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45396352 | |||||
chr10:45396386
|
G | A | 42 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(39): Show | 46 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.431+450G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396386 | ||||||
chr10:45396396
|
G | C | 13 | a0001c0003t0001g0055a0001c0003t0001g0056a0001c0003t0001g0058others(10): Show | 13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+460G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396396 | ||||||
chr10:45396397
|
A | T | 13 | a0001c0003t0001g0055a0001c0003t0001g0056a0001c0003t0001g0058others(10): Show | 13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+461A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396397 | ||||||
chr10:45396441
|
A | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0101others(1): Show | 6 | HG00621.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+505A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396441 | ||||||
chr10:45396492
|
C | T | 1 | a0001c0008t0002g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.431+556C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396492 | ||||||
chr10:45396572
|
A | G | 13 | a0001c0003t0001g0055a0001c0003t0001g0056a0001c0003t0001g0058others(10): Show | 13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+636A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396572 | ||||||
chr10:45396711
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.431+775C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396711 | ||||||
chr10:45396812
|
C | T | 44 | a0001c0001t0001g0077a0001c0001t0002g0305a0001c0002t0002g0004others(41): Show | 48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.431+876C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396812 | ||||||
chr10:45396950
|
T | G | 7 | a0001c0001t0001g0114a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG01192.hp1 HG01243.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+1014T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396950 | ||||||
chr10:45396983
|
A | G | 1 | a0001c0003t0001g0151 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.431+1047A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396983 | ||||||
chr10:45396984
|
T | C | 8 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(5): Show | 10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.431+1048T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45396984 | ||||||
chr10:45397109
|
G | A | 17 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.431+1173G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397109 | ||||||
chr10:45397210
|
G | A | 2 | a0001c0001t0001g0134a0001c0015t0001g0062 | 2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.431+1274G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397210 | ||||||
chr10:45397295
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+1359A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397295 | ||||||
chr10:45397344
|
C | G | 1 | a0001c0004t0001g0037 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.431+1408C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397344 | ||||||
chr10:45397369
|
C | T | 1 | a0001c0007t0001g0108 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.431+1433C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397369 | ||||||
chr10:45397413
|
A | C | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431+1477A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397413 | ||||||
chr10:45397516
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.431+1580G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397516 | ||||||
chr10:45397528
|
A | G | 8 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0141others(5): Show | 10 | HG02145.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.431+1592A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397528 | ||||||
chr10:45397929
|
A | C | 44 | a0001c0001t0002g0305a0001c0002t0002g0004a0001c0002t0002g0025others(41): Show | 48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.431+1993A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397929 | ||||||
chr10:45397931
|
G | A | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+1995G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397931 | ||||||
chr10:45397960
|
C | G | 42 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(39): Show | 46 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.431+2024C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45397960 | ||||||
chr10:45398068
|
AG | A | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+2134delG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45398068 | |||||
chr10:45398114
|
T | G | 6 | a0001c0002t0002g0280a0001c0002t0002g0281a0001c0002t0002g0282others(3): Show | 6 | NA18949.hp2 NA18959.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+2178T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398114 | ||||||
chr10:45398151
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+2215A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398151 | ||||||
chr10:45398172
|
G | A | 17 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.431+2236G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398172 | ||||||
chr10:45398353
|
G | A | 8 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(5): Show | 10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.431+2417G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398353 | ||||||
chr10:45398410
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.431+2474A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398410 | ||||||
chr10:45398558
|
T | G | 44 | a0001c0001t0002g0305a0001c0002t0002g0004a0001c0002t0002g0025others(41): Show | 48 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.431+2622T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398558 | ||||||
chr10:45398616
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.431+2680C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398616 | ||||||
chr10:45398761
|
T | C | 6 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0033others(3): Show | 8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.431+2825T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398761 | ||||||
chr10:45398803
|
C | T | 1 | a0001c0007t0001g0131 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.431+2867C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45398803 | ||||||
chr10:45399180
|
A | G | 1 | a0001c0001t0005g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.431+3244A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45399180 | ||||||
chr10:45399469
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.431+3533T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45399469 | ||||||
chr10:45399496
|
A | G | 6 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0003t0001g0174others(3): Show | 6 | HG01258.hp1 HG01358.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+3560A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45399496 | ||||||
chr10:45399751
|
C | T | 5 | a0001c0003t0001g0018a0001c0003t0001g0154a0001c0003t0001g0155others(2): Show | 6 | HG02486.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+3815C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45399751 | ||||||
chr10:45400132
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+4196T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400132 | ||||||
chr10:45400142
|
C | T | 1 | a0001c0001t0005g0076 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.431+4206C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400142 | ||||||
chr10:45400325
|
C | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(4): Show | 8 | HG02809.hp2 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.431+4389C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400325 | ||||||
chr10:45400326
|
G | A | 13 | a0001c0003t0001g0055a0001c0003t0001g0056a0001c0003t0001g0058others(10): Show | 13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+4390G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400326 | ||||||
chr10:45400337
|
C | T | 13 | a0001c0003t0001g0055a0001c0003t0001g0056a0001c0003t0001g0058others(10): Show | 13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.431+4401C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400337 | ||||||
chr10:45400400
|
G | A | 2 | a0003c0010t0001g0245a0003c0010t0001g0246 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.431+4464G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400400 | ||||||
chr10:45400400
|
GACCA | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+4468_431+4471d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45400400 | |||||
chr10:45400412
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.431+4476C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400412 | ||||||
chr10:45400429
|
A | G | 35 | a0001c0002t0002g0025a0001c0002t0002g0026a0001c0002t0002g0261others(32): Show | 37 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.431+4493A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400429 | ||||||
chr10:45400474
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.431+4538C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400474 | ||||||
chr10:45400521
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0019others(91): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.431+4585C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400521 | ||||||
chr10:45400579
|
A | G | 1 | a0001c0003t0001g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.431+4643A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400579 | ||||||
chr10:45400759
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(255): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.431+4823G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400759 | ||||||
chr10:45400803
|
A | G | 70 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(67): Show | 75 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.431+4867A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45400803 | ||||||
chr10:45400869
|
TATA | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+4936_431+4938d others(5): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45400869 | |||||
chr10:45401178
|
A | G | 1 | a0001c0004t0001g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.431+5242A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401178 | ||||||
chr10:45401223
|
A | T | 1 | a0001c0002t0002g0292 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.431+5287A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401223 | ||||||
chr10:45401279
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.431+5343T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401279 | ||||||
chr10:45401358
|
C | T | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+5422C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401358 | ||||||
chr10:45401359
|
T | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+5423T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401359 | ||||||
chr10:45401360
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+5424C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401360 | ||||||
chr10:45401413
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02071.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.431+5477G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401413 | ||||||
chr10:45401437
|
T | C | 1 | a0001c0002t0006g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.431+5501T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401437 | ||||||
chr10:45401675
|
G | A | 1 | a0001c0002t0002g0280 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.431+5739G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401675 | ||||||
chr10:45401707
|
A | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(267): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.431+5771A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401707 | ||||||
chr10:45401825
|
T | G | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.431+5889T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401825 | ||||||
chr10:45401858
|
G | A | 3 | a0001c0001t0002g0306a0001c0008t0002g0259a0001c0008t0002g0260 | 3 | HG02109.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.431+5922G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45401858 | ||||||
chr10:45402004
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.431+6068G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402004 | ||||||
chr10:45402036
|
G | A | 2 | a0001c0001t0001g0083a0001c0004t0001g0009 | 3 | HG02056.hp2 HG02083.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.431+6100G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402036 | ||||||
chr10:45402072
|
G | T | 26 | a0001c0003t0001g0006a0001c0003t0001g0016a0001c0003t0001g0017others(23): Show | 31 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.431+6136G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402072 | ||||||
chr10:45402073
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.431+6137C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402073 | ||||||
chr10:45402086
|
C | CA | 15 | a0001c0001t0001g0019a0001c0001t0001g0066a0001c0001t0001g0126others(12): Show | 16 | HG01975.hp1 HG02040.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.431+6170dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402086 | |||||
chr10:45402086
|
C | CAA | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(189): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.431+6169_431+6170d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402086 | |||||
chr10:45402086
|
C | CAAA | 38 | a0001c0001t0001g0022a0001c0001t0001g0115a0001c0001t0001g0133others(35): Show | 40 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.431+6168_431+6170d others(5): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402086 | |||||
chr10:45402086
|
CAAAAAA | C | 5 | a0001c0003t0001g0018a0001c0003t0001g0154a0001c0003t0001g0155others(2): Show | 6 | HG02486.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+6165_431+6170d others(8): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402086 | |||||
chr10:45402299
|
T | C | 1 | a0001c0019t0001g0213 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.431+6363T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402299 | ||||||
chr10:45402409
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+6473C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402409 | ||||||
chr10:45402413
|
G | A | 42 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0026others(39): Show | 46 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.431+6477G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402413 | ||||||
chr10:45402453
|
GCATCTCG others(4): Show |
G | 1 | a0001c0001t0001g0197 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.431+6520_431+6530d others(13): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402453 | |||||
chr10:45402601
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.431+6665G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402601 | ||||||
chr10:45402693
|
C | G | 1 | a0001c0001t0001g0242 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.431+6757C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402693 | ||||||
chr10:45402701
|
A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0279 | 2 | HG01433.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.431+6765A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402701 | ||||||
chr10:45402709
|
ACT | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | NA18954.hp1 NA18955.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.431+6776_431+6777d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45402709 | |||||
chr10:45402792
|
C | T | 1 | a0001c0021t0006g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.431+6856C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402792 | ||||||
chr10:45402908
|
C | A | 68 | a0001c0001t0001g0165a0001c0001t0001g0181a0001c0001t0001g0182others(65): Show | 73 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.431+6972C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402908 | ||||||
chr10:45402910
|
C | G | 11 | a0001c0001t0001g0024a0001c0001t0001g0169a0001c0001t0001g0170others(8): Show | 12 | HG00621.hp1 HG01106.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.431+6974C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45402910 | ||||||
chr10:45403034
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+7098T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403034 | ||||||
chr10:45403043
|
G | A | 2 | a0001c0008t0002g0259a0001c0008t0002g0260 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.431+7107G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403043 | ||||||
chr10:45403046
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.431+7110A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403046 | ||||||
chr10:45403071
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0179a0001c0001t0001g0180 | 6 | NA18944.hp2 NA18947.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.431+7135G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403071 | ||||||
chr10:45403216
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+7280C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403216 | ||||||
chr10:45403320
|
C | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+7384C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403320 | ||||||
chr10:45403465
|
G | A | 21 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(18): Show | 22 | HG01069.hp1 HG02071.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.431+7529G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403465 | ||||||
chr10:45403587
|
G | A | 1 | a0001c0003t0001g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431+7651G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403587 | ||||||
chr10:45403811
|
G | A | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+7875G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403811 | ||||||
chr10:45403901
|
A | G | 1 | a0001c0002t0002g0288 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.431+7965A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403901 | ||||||
chr10:45403934
|
C | T | 7 | a0001c0001t0001g0015a0001c0004t0001g0129a0001c0007t0001g0015others(4): Show | 7 | NA18941.hp1 NA18949.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+7998C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45403934 | ||||||
chr10:45404147
|
T | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-8044T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45404147 | ||||||
chr10:45404255
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.432-7936A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45404255 | ||||||
chr10:45404660
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.432-7531C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45404660 | ||||||
chr10:45404885
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.432-7306A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45404885 | ||||||
chr10:45404979
|
A | G | 1 | a0001c0002t0002g0268 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.432-7212A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45404979 | ||||||
chr10:45405042
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-7149C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405042 | ||||||
chr10:45405244
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.432-6947G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405244 | ||||||
chr10:45405281
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(219): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.432-6910G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405281 | ||||||
chr10:45405369
|
C | T | 1 | a0001c0002t0007g0307 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.432-6822C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405369 | ||||||
chr10:45405384
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0227others(1): Show | 7 | HG01255.hp2 HG01346.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.432-6807T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405384 | ||||||
chr10:45405422
|
A | G | 3 | a0001c0002t0002g0309a0001c0002t0002g0310a0001c0002t0002g0311 | 3 | HG01243.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.432-6769A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405422 | ||||||
chr10:45405523
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.432-6668G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405523 | ||||||
chr10:45405588
|
A | G | 4 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0033others(1): Show | 6 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.432-6603A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405588 | ||||||
chr10:45405593
|
T | A | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-6598T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405593 | ||||||
chr10:45405641
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.432-6550A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405641 | ||||||
chr10:45405653
|
C | T | 13 | a0001c0003t0001g0055a0001c0003t0001g0056a0001c0003t0001g0058others(10): Show | 13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.432-6538C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45405653 | ||||||
chr10:45405739
|
C | CTTT | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-6439_432-6437d others(5): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45405739 | |||||
chr10:45405739
|
CT | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(157): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.432-6437delT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45405739 | |||||
chr10:45405739
|
CTT | C | 23 | a0001c0001t0001g0192a0001c0001t0002g0306a0001c0002t0002g0004others(20): Show | 25 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.432-6438_432-6437d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45405739 | |||||
chr10:45406009
|
G | T | 1 | a0001c0001t0001g0197 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.432-6182G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406009 | ||||||
chr10:45406234
|
G | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0004t0001g0037others(3): Show | 6 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-5957G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406234 | ||||||
chr10:45406267
|
C | A | 5 | a0001c0001t0001g0165a0001c0004t0001g0037a0001c0004t0001g0038others(2): Show | 5 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.432-5924C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406267 | ||||||
chr10:45406268
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0132 | 2 | NA19058.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.432-5923G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406268 | ||||||
chr10:45406395
|
G | A | 3 | a0001c0003t0001g0154a0001c0003t0001g0163a0001c0006t0009g0153 | 3 | HG02486.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.432-5796G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406395 | ||||||
chr10:45406400
|
A | G | 1 | a0001c0004t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.432-5791A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406400 | ||||||
chr10:45406423
|
T | A | 31 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0305others(28): Show | 33 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.432-5768T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406423 | ||||||
chr10:45406492
|
G | A | 13 | a0001c0003t0001g0055a0001c0003t0001g0056a0001c0003t0001g0058others(10): Show | 13 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.432-5699G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406492 | ||||||
chr10:45406607
|
A | G | 17 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.432-5584A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406607 | ||||||
chr10:45406671
|
T | C | 49 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(46): Show | 52 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.432-5520T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406671 | ||||||
chr10:45406959
|
T | C | 3 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG02080.hp1 NA18975.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.432-5232T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45406959 | ||||||
chr10:45407064
|
T | C | 2 | a0002c0005t0003g0120a0002c0005t0003g0121 | 2 | NA18998.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.432-5127T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407064 | ||||||
chr10:45407089
|
G | T | 24 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(21): Show | 25 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.432-5102G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407089 | ||||||
chr10:45407257
|
C | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | NA18961.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.432-4934C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407257 | ||||||
chr10:45407362
|
T | A | 24 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(21): Show | 25 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.432-4829T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407362 | ||||||
chr10:45407391
|
CT | C | 61 | a0001c0001t0001g0077a0001c0001t0001g0179a0001c0002t0002g0025others(58): Show | 68 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.432-4789delT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45407391 | |||||
chr10:45407400
|
T | A | 1 | a0001c0002t0006g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.432-4791T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407400 | ||||||
chr10:45407402
|
T | C | 5 | a0001c0001t0001g0074a0001c0001t0002g0305a0001c0002t0002g0270others(2): Show | 5 | HG02615.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.432-4789T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407402 | ||||||
chr10:45407403
|
C | T | 20 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(17): Show | 21 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.432-4788C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407403 | ||||||
chr10:45407404
|
C | T | 24 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181others(21): Show | 25 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.432-4787C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407404 | ||||||
chr10:45407438
|
C | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(251): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.432-4753C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407438 | ||||||
chr10:45407464
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(267): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.432-4727A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407464 | ||||||
chr10:45407490
|
A | G | 1 | a0001c0002t0002g0297 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.432-4701A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407490 | ||||||
chr10:45407587
|
C | T | 3 | a0001c0004t0001g0007a0001c0004t0001g0064a0001c0004t0001g0065 | 4 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.432-4604C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407587 | ||||||
chr10:45407785
|
C | A | 1 | a0001c0001t0001g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432-4406C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407785 | ||||||
chr10:45407905
|
T | G | 1 | a0001c0002t0002g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.432-4286T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407905 | ||||||
chr10:45407919
|
G | A | 25 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(22): Show | 27 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.432-4272G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45407919 | ||||||
chr10:45408230
|
T | C | 2 | a0001c0011t0002g0257a0001c0011t0002g0258 | 2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.432-3961T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408230 | ||||||
chr10:45408231
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.432-3960G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408231 | ||||||
chr10:45408239
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(138): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.432-3952C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408239 | ||||||
chr10:45408318
|
T | A | 20 | a0001c0001t0002g0306a0001c0002t0002g0004a0001c0002t0002g0263others(17): Show | 22 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.432-3873T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408318 | ||||||
chr10:45408539
|
G | T | 20 | a0001c0001t0002g0306a0001c0002t0002g0004a0001c0002t0002g0263others(17): Show | 22 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.432-3652G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408539 | ||||||
chr10:45408568
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(138): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.432-3623A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408568 | ||||||
chr10:45408578
|
G | T | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.432-3613G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408578 | ||||||
chr10:45408593
|
C | T | 1 | a0001c0004t0001g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.432-3598C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408593 | ||||||
chr10:45408613
|
G | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0084 | 2 | HG02965.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.432-3578G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408613 | ||||||
chr10:45408817
|
C | T | 1 | a0002c0005t0003g0241 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.432-3374C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45408817 | ||||||
chr10:45409266
|
G | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(171): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.432-2925G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409266 | ||||||
chr10:45409271
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.432-2920C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409271 | ||||||
chr10:45409304
|
T | C | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.432-2887T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409304 | ||||||
chr10:45409323
|
A | ACT | 256 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(253): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.432-2867_432-2866d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409323 | |||||
chr10:45409411
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.432-2780T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409411 | ||||||
chr10:45409432
|
C | T | 1 | a0002c0005t0003g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.432-2759C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409432 | ||||||
chr10:45409509
|
G | GTC | 87 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0063others(84): Show | 96 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.432-2658_432-2657d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | |||||
chr10:45409509
|
G | GTCTC | 14 | a0001c0001t0001g0165a0001c0001t0001g0236a0001c0002t0002g0292others(11): Show | 14 | HG01123.hp1 HG01192.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.432-2660_432-2657d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | |||||
chr10:45409509
|
G | GTCTCTC | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(97): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.432-2662_432-2657d others(8): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | |||||
chr10:45409509
|
G | GTCTCTCT others(1): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0125a0001c0001t0001g0214others(2): Show | 6 | HG01070.hp1 HG01071.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-2664_432-2657d others(10): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | |||||
chr10:45409509
|
G | GTCTCTCT others(3): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0134 | 2 | HG02886.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.432-2666_432-2657d others(12): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | |||||
chr10:45409509
|
GTCTC | G | 11 | a0001c0003t0001g0055a0001c0003t0001g0058a0001c0003t0004g0047others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.432-2660_432-2657d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409509 | |||||
chr10:45409513
|
C | G | 2 | a0002c0005t0003g0039a0002c0005t0003g0040 | 2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.432-2678C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409513 | ||||||
chr10:45409527
|
C | CTCTCTCT others(5): Show |
1 | a0001c0009t0001g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.432-2657_432-2656i others(14): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409527 | |||||
chr10:45409569
|
TTCTC | T | 5 | a0001c0001t0008g0255a0001c0004t0001g0037a0001c0004t0001g0038others(2): Show | 5 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.432-2606_432-2603d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409569 | |||||
chr10:45409593
|
CTCTG | C | 20 | a0001c0001t0002g0306a0001c0002t0002g0004a0001c0002t0002g0263others(17): Show | 22 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.432-2594_432-2591d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 45409593 | |||||
chr10:45409662
|
C | T | 11 | a0001c0003t0001g0055a0001c0003t0001g0058a0001c0003t0004g0047others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.432-2529C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409662 | ||||||
chr10:45409788
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.432-2403G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409788 | ||||||
chr10:45409877
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0101 | 3 | HG01256.hp1 HG01258.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.432-2314G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45409877 | ||||||
chr10:45410076
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.432-2115G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410076 | ||||||
chr10:45410097
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.432-2094T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410097 | ||||||
chr10:45410122
|
A | G | 1 | a0001c0021t0006g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.432-2069A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410122 | ||||||
chr10:45410240
|
G | A | 2 | a0001c0001t0002g0305a0001c0008t0002g0259 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.432-1951G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410240 | ||||||
chr10:45410274
|
G | T | 2 | a0001c0001t0001g0067a0001c0015t0001g0062 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.432-1917G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410274 | ||||||
chr10:45410352
|
A | G | 8 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(5): Show | 10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.432-1839A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410352 | ||||||
chr10:45410446
|
T | C | 12 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(9): Show | 13 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.432-1745T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410446 | ||||||
chr10:45410551
|
C | A | 1 | a0001c0006t0009g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.432-1640C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410551 | ||||||
chr10:45410584
|
A | C | 1 | a0001c0021t0006g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.432-1607A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410584 | ||||||
chr10:45410926
|
G | C | 1 | a0002c0005t0003g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.432-1265G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45410926 | ||||||
chr10:45411064
|
T | C | 2 | a0001c0011t0002g0257a0001c0011t0002g0258 | 2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.432-1127T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411064 | ||||||
chr10:45411125
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0019others(70): Show | 82 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.432-1066G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411125 | ||||||
chr10:45411171
|
A | C | 8 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(5): Show | 10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.432-1020A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411171 | ||||||
chr10:45411245
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.432-946G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411245 | ||||||
chr10:45411516
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0161 | 2 | HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.432-675C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411516 | ||||||
chr10:45411688
|
G | T | 27 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(24): Show | 29 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.432-503G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411688 | ||||||
chr10:45411754
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.432-437C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411754 | ||||||
chr10:45411839
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.432-352C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411839 | ||||||
chr10:45411914
|
A | G | 11 | a0001c0007t0001g0108a0002c0005t0003g0036a0002c0005t0003g0113others(8): Show | 11 | HG02040.hp1 HG02080.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.432-277A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411914 | ||||||
chr10:45411952
|
A | G | 36 | a0001c0001t0001g0066a0001c0001t0001g0157a0001c0002t0002g0025others(33): Show | 39 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.432-239A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45411952 | ||||||
chr10:45412006
|
G | C | 43 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0063others(40): Show | 47 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.432-185G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45412006 | ||||||
chr10:45412078
|
G | A | 10 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(7): Show | 12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.432-113G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45412078 | ||||||
chr10:45412088
|
A | G | 1 | a0001c0003t0001g0151 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.432-103A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45412088 | ||||||
chr10:45412106
|
G | A | 1 | a0001c0006t0001g0005 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.432-85G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 3/13 | chr10 | 45412106 | ||||||
chr10:45412314
|
G | A | 1 | a0001c0003t0001g0148 | 1 | HG02717.hp2 | splice_donor_variant&intron_variant | HIGH | c.554+1G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412314 | ||||||
chr10:45412474
|
G | A | 1 | a0001c0002t0002g0309 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.554+161G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412474 | ||||||
chr10:45412526
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.554+213A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412526 | ||||||
chr10:45412730
|
G | T | 1 | a0001c0001t0001g0238 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.554+417G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412730 | ||||||
chr10:45412768
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.554+455T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412768 | ||||||
chr10:45412954
|
G | A | 3 | a0001c0003t0001g0154a0001c0003t0001g0163a0001c0006t0009g0153 | 3 | HG02486.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.554+641G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412954 | ||||||
chr10:45412977
|
T | C | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.554+664T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45412977 | ||||||
chr10:45413312
|
T | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(253): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.554+999T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413312 | ||||||
chr10:45413314
|
G | A | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+1001G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413314 | ||||||
chr10:45413546
|
C | T | 1 | a0001c0004t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.554+1233C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413546 | ||||||
chr10:45413569
|
C | T | 7 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(4): Show | 9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+1256C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413569 | ||||||
chr10:45413570
|
A | G | 8 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(5): Show | 10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+1257A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413570 | ||||||
chr10:45413644
|
A | G | 10 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(7): Show | 12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+1331A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413644 | ||||||
chr10:45413656
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0022others(65): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.554+1343C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413656 | ||||||
chr10:45413698
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.554+1385C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413698 | ||||||
chr10:45413798
|
AACAG | A | 20 | a0001c0001t0002g0306a0001c0002t0002g0004a0001c0002t0002g0263others(17): Show | 22 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.554+1494_554+1497d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45413798 | |||||
chr10:45413807
|
A | C | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.554+1494A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413807 | ||||||
chr10:45413826
|
A | G | 11 | a0001c0003t0001g0055a0001c0003t0001g0058a0001c0003t0004g0047others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.554+1513A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413826 | ||||||
chr10:45413913
|
C | G | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+1600C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413913 | ||||||
chr10:45413987
|
T | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.554+1674T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45413987 | ||||||
chr10:45414120
|
G | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0305others(1): Show | 4 | HG01192.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+1807G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414120 | ||||||
chr10:45414187
|
A | G | 3 | a0001c0002t0002g0309a0001c0002t0002g0310a0001c0002t0002g0311 | 3 | HG01243.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.554+1874A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414187 | ||||||
chr10:45414193
|
C | T | 11 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(8): Show | 13 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.554+1880C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414193 | ||||||
chr10:45414398
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2085A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414398 | ||||||
chr10:45414400
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2087G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414400 | ||||||
chr10:45414403
|
G | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2090G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414403 | ||||||
chr10:45414404
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2091G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414404 | ||||||
chr10:45414409
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2096C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414409 | ||||||
chr10:45414413
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2100C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414413 | ||||||
chr10:45414421
|
T | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2108T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414421 | ||||||
chr10:45414436
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2123T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414436 | ||||||
chr10:45414444
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2131G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414444 | ||||||
chr10:45414452
|
T | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2139T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414452 | ||||||
chr10:45414459
|
A | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2146A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414459 | ||||||
chr10:45414461
|
G | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2148G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414461 | ||||||
chr10:45414463
|
T | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2150T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414463 | ||||||
chr10:45414468
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2155C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414468 | ||||||
chr10:45414472
|
A | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2159A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414472 | ||||||
chr10:45414475
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2162C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414475 | ||||||
chr10:45414476
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+2163A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414476 | ||||||
chr10:45414484
|
C | T | 20 | a0001c0001t0002g0306a0001c0002t0002g0004a0001c0002t0002g0263others(17): Show | 22 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.554+2171C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414484 | ||||||
chr10:45414521
|
G | A | 1 | a0001c0011t0002g0257 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.554+2208G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414521 | ||||||
chr10:45414585
|
A | G | 8 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(5): Show | 10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+2272A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414585 | ||||||
chr10:45414642
|
T | G | 3 | a0001c0011t0002g0257a0001c0011t0002g0258a0001c0015t0001g0062 | 3 | HG00741.hp2 HG01192.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.554+2329T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414642 | ||||||
chr10:45414822
|
A | G | 7 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(4): Show | 8 | HG02109.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.554+2509A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414822 | ||||||
chr10:45414840
|
A | G | 1 | a0001c0002t0002g0289 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.554+2527A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414840 | ||||||
chr10:45414894
|
T | C | 2 | a0001c0003t0001g0154a0001c0006t0009g0153 | 2 | HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.554+2581T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414894 | ||||||
chr10:45414952
|
T | A | 2 | a0001c0001t0001g0254a0001c0001t0008g0255 | 2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.554+2639T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414952 | ||||||
chr10:45414992
|
G | A | 2 | a0001c0004t0001g0008a0001c0004t0001g0068 | 3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.554+2679G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45414992 | ||||||
chr10:45415099
|
G | T | 2 | a0002c0005t0003g0039a0002c0005t0003g0040 | 2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.554+2786G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415099 | ||||||
chr10:45415148
|
T | C | 8 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(5): Show | 10 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.554+2835T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415148 | ||||||
chr10:45415328
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.554+3015C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415328 | ||||||
chr10:45415581
|
T | TA | 159 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(156): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.554+3277dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45415581 | |||||
chr10:45415583
|
A | AT | 71 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0022others(68): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.554+3270_554+3271i others(3): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415583 | ||||||
chr10:45415599
|
C | T | 4 | a0001c0003t0001g0006a0001c0003t0001g0032a0001c0003t0001g0033others(1): Show | 6 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.554+3286C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415599 | ||||||
chr10:45415603
|
A | G | 4 | a0001c0004t0001g0037a0001c0004t0001g0038a0002c0005t0003g0039others(1): Show | 4 | HG01243.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+3290A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415603 | ||||||
chr10:45415653
|
G | A | 14 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0164others(11): Show | 16 | HG01192.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.554+3340G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415653 | ||||||
chr10:45415690
|
C | A | 1 | a0001c0021t0006g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.554+3377C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415690 | ||||||
chr10:45415844
|
G | A | 10 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(7): Show | 12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+3531G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415844 | ||||||
chr10:45415871
|
T | C | 1 | a0001c0004t0001g0038 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.554+3558T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45415871 | ||||||
chr10:45416240
|
A | C | 7 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(4): Show | 9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+3927A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416240 | ||||||
chr10:45416354
|
A | G | 1 | a0001c0021t0006g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.554+4041A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416354 | ||||||
chr10:45416383
|
A | G | 5 | a0001c0001t0001g0212a0001c0001t0001g0228a0001c0001t0001g0229others(2): Show | 5 | NA18939.hp2 NA18944.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.554+4070A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416383 | ||||||
chr10:45416438
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.554+4125C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416438 | ||||||
chr10:45416516
|
A | G | 2 | a0001c0001t0002g0305a0001c0008t0002g0259 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.554+4203A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416516 | ||||||
chr10:45416671
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.554+4358G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416671 | ||||||
chr10:45416706
|
GATGA | G | 25 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(22): Show | 27 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.554+4397_554+4400d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45416706 | |||||
chr10:45416761
|
A | G | 3 | a0001c0003t0001g0154a0001c0003t0001g0163a0001c0006t0009g0153 | 3 | HG02486.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.554+4448A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416761 | ||||||
chr10:45416789
|
T | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(22): Show | 27 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.554+4476T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416789 | ||||||
chr10:45416817
|
GGATGGAT others(20): Show |
G | 5 | a0001c0001t0001g0165a0001c0004t0001g0037a0001c0004t0001g0038others(2): Show | 5 | HG01192.hp1 HG01243.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.554+4520_554+4546d others(29): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45416817 | |||||
chr10:45416987
|
A | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0105 | 3 | NA18983.hp2 NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.554+4674A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416987 | ||||||
chr10:45416991
|
T | A | 1 | a0001c0020t0001g0221 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.554+4678T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45416991 | ||||||
chr10:45417056
|
G | A | 7 | a0001c0002t0002g0004a0001c0002t0002g0263a0001c0002t0002g0285others(4): Show | 9 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+4743G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417056 | ||||||
chr10:45417323
|
T | G | 28 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(25): Show | 30 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.554+5010T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417323 | ||||||
chr10:45417700
|
A | G | 10 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(7): Show | 12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+5387A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417700 | ||||||
chr10:45417728
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.554+5415G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417728 | ||||||
chr10:45417872
|
A | G | 10 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(7): Show | 12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.554+5559A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417872 | ||||||
chr10:45417879
|
C | T | 3 | a0001c0011t0002g0257a0001c0011t0002g0258a0001c0015t0001g0062 | 3 | HG00741.hp2 HG01192.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.554+5566C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417879 | ||||||
chr10:45417964
|
C | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0157 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+5651C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45417964 | ||||||
chr10:45418288
|
G | A | 2 | a0001c0001t0005g0042a0001c0001t0005g0076 | 2 | HG01346.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.555-5753G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45418288 | ||||||
chr10:45418429
|
G | A | 1 | a0001c0002t0002g0271 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.555-5612G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45418429 | ||||||
chr10:45418437
|
C | CT | 10 | a0001c0003t0001g0055a0001c0003t0001g0058a0001c0003t0004g0047others(7): Show | 10 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.555-5603dupT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45418437 | |||||
chr10:45418690
|
A | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(7): Show | 12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-5351A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45418690 | ||||||
chr10:45418691
|
G | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0167others(7): Show | 12 | HG02109.hp2 HG02258.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-5350G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45418691 | ||||||
chr10:45418839
|
G | C | 1 | a0001c0002t0002g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.555-5202G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45418839 | ||||||
chr10:45419055
|
C | T | 1 | a0001c0002t0002g0296 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.555-4986C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419055 | ||||||
chr10:45419079
|
C | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(202): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.555-4962C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419079 | ||||||
chr10:45419250
|
C | T | 1 | a0001c0006t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.555-4791C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419250 | ||||||
chr10:45419296
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(144): Show | 162 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.555-4745G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419296 | ||||||
chr10:45419302
|
G | C | 2 | a0001c0001t0002g0306a0001c0006t0001g0142 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.555-4739G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419302 | ||||||
chr10:45419305
|
CG | C | 94 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0046others(91): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.555-4729delG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45419305 | |||||
chr10:45419324
|
G | A | 13 | a0001c0001t0001g0063a0001c0001t0001g0167a0001c0004t0001g0007others(10): Show | 16 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.555-4717G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419324 | ||||||
chr10:45419426
|
A | G | 4 | a0001c0002t0002g0309a0001c0003t0001g0154a0001c0003t0001g0163others(1): Show | 4 | HG02970.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-4615A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419426 | ||||||
chr10:45419455
|
G | A | 2 | a0001c0004t0001g0037a0001c0004t0001g0068 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.555-4586G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419455 | ||||||
chr10:45419471
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.555-4570G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419471 | ||||||
chr10:45419666
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.555-4375G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419666 | ||||||
chr10:45419707
|
C | A | 12 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0167others(9): Show | 14 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.555-4334C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419707 | ||||||
chr10:45419710
|
G | T | 11 | a0001c0001t0001g0063a0001c0001t0001g0167a0001c0004t0001g0007others(8): Show | 13 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.555-4331G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419710 | ||||||
chr10:45419737
|
T | TCAAAAGA others(6): Show |
254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(251): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.555-4298_555-4297i others(15): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 45419737 | |||||
chr10:45419804
|
G | C | 17 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0167others(14): Show | 21 | HG01243.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.555-4237G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419804 | ||||||
chr10:45419816
|
A | C | 17 | a0001c0006t0001g0005a0002c0005t0003g0036a0002c0005t0003g0039others(14): Show | 18 | HG01243.hp2 HG01884.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.555-4225A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419816 | ||||||
chr10:45419871
|
G | C | 11 | a0001c0001t0001g0063a0001c0001t0001g0167a0001c0004t0001g0007others(8): Show | 13 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.555-4170G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419871 | ||||||
chr10:45419886
|
G | C | 1 | a0001c0006t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.555-4155G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419886 | ||||||
chr10:45419892
|
A | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(237): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.555-4149A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419892 | ||||||
chr10:45419923
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.555-4118G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45419923 | ||||||
chr10:45420206
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.555-3835G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420206 | ||||||
chr10:45420245
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.555-3796C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420245 | ||||||
chr10:45420304
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.555-3737G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420304 | ||||||
chr10:45420321
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0069others(1): Show | 5 | HG01070.hp1 HG01071.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-3720A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420321 | ||||||
chr10:45420374
|
C | G | 1 | a0001c0020t0001g0221 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.555-3667C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420374 | ||||||
chr10:45420398
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0006t0009g0153 | 3 | HG02486.hp1 HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.555-3643G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420398 | ||||||
chr10:45420407
|
C | T | 1 | a0001c0021t0006g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.555-3634C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420407 | ||||||
chr10:45420477
|
C | A | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.555-3564C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420477 | ||||||
chr10:45420493
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(197): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.555-3548C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420493 | ||||||
chr10:45420540
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.555-3501C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420540 | ||||||
chr10:45420680
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.555-3361C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420680 | ||||||
chr10:45420778
|
T | A | 14 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(11): Show | 15 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.555-3263T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420778 | ||||||
chr10:45420788
|
G | A | 14 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(11): Show | 15 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.555-3253G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420788 | ||||||
chr10:45420818
|
G | A | 2 | a0001c0002t0002g0274a0001c0002t0002g0297 | 2 | HG00099.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.555-3223G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420818 | ||||||
chr10:45420837
|
G | A | 4 | a0001c0002t0002g0310a0001c0002t0002g0311a0001c0003t0001g0016others(1): Show | 5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-3204G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420837 | ||||||
chr10:45420901
|
C | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0216 | 2 | NA18946.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.555-3140C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420901 | ||||||
chr10:45420902
|
G | C | 18 | a0001c0001t0001g0164a0001c0006t0001g0144a0002c0005t0003g0036others(15): Show | 18 | HG01243.hp2 HG02040.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.555-3139G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45420902 | ||||||
chr10:45421386
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(243): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.555-2655T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421386 | ||||||
chr10:45421465
|
C | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(243): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.555-2576C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421465 | ||||||
chr10:45421466
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0069others(1): Show | 5 | HG01070.hp1 HG01071.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-2575G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421466 | ||||||
chr10:45421639
|
A | G | 1 | a0001c0002t0002g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.555-2402A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421639 | ||||||
chr10:45421644
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(241): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.555-2397A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421644 | ||||||
chr10:45421669
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(212): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.555-2372T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421669 | ||||||
chr10:45421751
|
A | G | 18 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0060others(15): Show | 19 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.555-2290A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421751 | ||||||
chr10:45421868
|
T | C | 18 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0060others(15): Show | 19 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.555-2173T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421868 | ||||||
chr10:45421895
|
C | A | 1 | a0001c0001t0001g0088 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.555-2146C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421895 | ||||||
chr10:45421928
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(209): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.555-2113C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45421928 | ||||||
chr10:45422033
|
G | A | 4 | a0001c0002t0002g0310a0001c0002t0002g0311a0001c0003t0001g0016others(1): Show | 5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-2008G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422033 | ||||||
chr10:45422094
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0214 | 3 | HG01361.hp2 HG01516.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.555-1947T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422094 | ||||||
chr10:45422293
|
C | G | 33 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0060others(30): Show | 34 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.555-1748C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422293 | ||||||
chr10:45422299
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.555-1742G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422299 | ||||||
chr10:45422379
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.555-1662G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422379 | ||||||
chr10:45422409
|
C | A | 1 | a0001c0006t0001g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.555-1632C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422409 | ||||||
chr10:45422628
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(257): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.555-1413A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422628 | ||||||
chr10:45422645
|
C | T | 15 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0001t0002g0305others(12): Show | 15 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.555-1396C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422645 | ||||||
chr10:45422646
|
G | A | 1 | a0001c0002t0002g0283 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.555-1395G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422646 | ||||||
chr10:45422831
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(257): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.555-1210C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422831 | ||||||
chr10:45422932
|
C | T | 21 | a0001c0001t0001g0194a0001c0001t0001g0254a0001c0003t0001g0056others(18): Show | 25 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.555-1109C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45422932 | ||||||
chr10:45423033
|
G | A | 1 | a0001c0006t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.555-1008G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423033 | ||||||
chr10:45423051
|
C | T | 1 | a0001c0004t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.555-990C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423051 | ||||||
chr10:45423264
|
G | A | 1 | a0001c0003t0001g0141 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.555-777G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423264 | ||||||
chr10:45423283
|
A | G | 1 | a0001c0006t0001g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.555-758A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423283 | ||||||
chr10:45423366
|
C | T | 1 | a0001c0001t0001g0021 | 2 | NA18945.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.555-675C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423366 | ||||||
chr10:45423567
|
G | A | 1 | a0001c0002t0002g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.555-474G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423567 | ||||||
chr10:45423609
|
A | G | 33 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0060others(30): Show | 34 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.555-432A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423609 | ||||||
chr10:45423628
|
A | C | 1 | a0001c0002t0002g0309 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.555-413A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423628 | ||||||
chr10:45423666
|
G | T | 1 | a0001c0008t0002g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.555-375G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423666 | ||||||
chr10:45423668
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.555-373C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423668 | ||||||
chr10:45423686
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.555-355C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423686 | ||||||
chr10:45423711
|
G | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0060others(30): Show | 34 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.555-330G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423711 | ||||||
chr10:45423885
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.555-156G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423885 | ||||||
chr10:45423941
|
G | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0069others(8): Show | 12 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.555-100G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423941 | ||||||
chr10:45423945
|
G | A | 4 | a0001c0002t0002g0310a0001c0002t0002g0311a0001c0003t0001g0016others(1): Show | 5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-96G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423945 | ||||||
chr10:45423976
|
T | C | 1 | a0002c0005t0003g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.555-65T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423976 | ||||||
chr10:45423983
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.555-58G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 4/13 | chr10 | 45423983 | ||||||
chr10:45424168
|
C | T | 2 | a0001c0001t0005g0042a0001c0001t0005g0076 | 2 | HG01346.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.661+21C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424168 | ||||||
chr10:45424274
|
T | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(30): Show | 36 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.661+127T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424274 | ||||||
chr10:45424279
|
C | G | 4 | a0001c0002t0002g0310a0001c0002t0002g0311a0001c0003t0001g0016others(1): Show | 5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+132C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424279 | ||||||
chr10:45424378
|
C | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0060others(15): Show | 19 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.661+231C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424378 | ||||||
chr10:45424528
|
A | G | 4 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0112others(1): Show | 4 | HG01099.hp2 HG02622.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+381A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424528 | ||||||
chr10:45424651
|
G | C | 1 | a0001c0001t0001g0216 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.662-309G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424651 | ||||||
chr10:45424657
|
C | A | 1 | a0001c0008t0002g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.662-303C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424657 | ||||||
chr10:45424680
|
C | T | 1 | a0001c0001t0005g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.662-280C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424680 | ||||||
chr10:45424791
|
G | C | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.662-169G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424791 | ||||||
chr10:45424830
|
G | A | 1 | a0001c0002t0002g0309 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.662-130G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424830 | ||||||
chr10:45424897
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.662-63G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 5/13 | chr10 | 45424897 | ||||||
chr10:45425257
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(214): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.834+125C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425257 | ||||||
chr10:45425366
|
G | A | 30 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0069others(27): Show | 32 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.834+234G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425366 | ||||||
chr10:45425396
|
A | G | 15 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0001t0002g0305others(12): Show | 15 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.834+264A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425396 | ||||||
chr10:45425461
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.834+329A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425461 | ||||||
chr10:45425570
|
C | A | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.834+438C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425570 | ||||||
chr10:45425744
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.834+612C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425744 | ||||||
chr10:45425895
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.834+763G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425895 | ||||||
chr10:45425903
|
G | T | 14 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0001t0004g0203others(11): Show | 14 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.834+771G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45425903 | ||||||
chr10:45426095
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.834+963C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426095 | ||||||
chr10:45426291
|
T | TG | 30 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0069others(27): Show | 32 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.834+1161dupG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 45426291 | |||||
chr10:45426315
|
G | A | 1 | a0001c0003t0001g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.834+1183G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426315 | ||||||
chr10:45426333
|
A | G | 1 | a0001c0021t0006g0291 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.834+1201A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426333 | ||||||
chr10:45426417
|
A | C | 30 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0069others(27): Show | 32 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.834+1285A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426417 | ||||||
chr10:45426418
|
A | C | 30 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0069others(27): Show | 32 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.834+1286A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426418 | ||||||
chr10:45426429
|
C | T | 57 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0023others(54): Show | 60 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.834+1297C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426429 | ||||||
chr10:45426534
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(214): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.834+1402A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426534 | ||||||
chr10:45426582
|
G | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0079a0001c0001t0001g0249 | 4 | NA18939.hp1 NA18950.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+1450G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426582 | ||||||
chr10:45426586
|
G | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0227others(1): Show | 7 | HG01255.hp2 HG01346.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+1454G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426586 | ||||||
chr10:45426742
|
G | A | 15 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0001t0002g0305others(12): Show | 15 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.834+1610G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426742 | ||||||
chr10:45426763
|
T | G | 1 | a0001c0009t0001g0081 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.834+1631T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426763 | ||||||
chr10:45426927
|
A | G | 1 | a0001c0002t0002g0278 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.835-1691A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426927 | ||||||
chr10:45426938
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.835-1680A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45426938 | ||||||
chr10:45427023
|
G | C | 1 | a0001c0004t0001g0233 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.835-1595G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427023 | ||||||
chr10:45427179
|
C | T | 15 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0001t0002g0305others(12): Show | 15 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.835-1439C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427179 | ||||||
chr10:45427282
|
C | T | 13 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(10): Show | 14 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.835-1336C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427282 | ||||||
chr10:45427353
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.835-1265C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427353 | ||||||
chr10:45427506
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG01361.hp1 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.835-1112C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427506 | ||||||
chr10:45427529
|
C | T | 4 | a0001c0002t0002g0310a0001c0002t0002g0311a0001c0003t0001g0016others(1): Show | 5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.835-1089C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427529 | ||||||
chr10:45427576
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.835-1042G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427576 | ||||||
chr10:45427577
|
G | A | 1 | a0001c0006t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.835-1041G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427577 | ||||||
chr10:45427617
|
A | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0069others(9): Show | 13 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.835-1001A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427617 | ||||||
chr10:45427720
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.835-898C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45427720 | ||||||
chr10:45428023
|
C | T | 1 | a0001c0006t0001g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.835-595C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428023 | ||||||
chr10:45428063
|
T | C | 42 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(39): Show | 45 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.835-555T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428063 | ||||||
chr10:45428080
|
C | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(202): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.835-538C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428080 | ||||||
chr10:45428098
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.835-520C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428098 | ||||||
chr10:45428133
|
G | C | 1 | a0001c0001t0001g0193 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.835-485G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428133 | ||||||
chr10:45428322
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(226): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.835-296A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428322 | ||||||
chr10:45428575
|
G | A | 252 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(249): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.835-43G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 6/13 | chr10 | 45428575 | ||||||
chr10:45428808
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(241): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.981+44T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45428808 | ||||||
chr10:45428909
|
A | T | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+145A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45428909 | ||||||
chr10:45429029
|
C | T | 1 | a0001c0006t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.981+265C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429029 | ||||||
chr10:45429235
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.981+471C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429235 | ||||||
chr10:45429366
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.981+602G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429366 | ||||||
chr10:45429436
|
C | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0069others(19): Show | 23 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.981+672C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429436 | ||||||
chr10:45429439
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.981+675T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429439 | ||||||
chr10:45429448
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.981+684T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429448 | ||||||
chr10:45429504
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0119 | 2 | HG01106.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.981+740C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429504 | ||||||
chr10:45429520
|
C | A | 31 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0060others(28): Show | 33 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.981+756C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429520 | ||||||
chr10:45429629
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.981+865G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429629 | ||||||
chr10:45429751
|
A | T | 1 | a0001c0006t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.981+987A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429751 | ||||||
chr10:45429758
|
T | G | 2 | a0002c0005t0003g0135a0002c0005t0003g0241 | 2 | NA18945.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.981+994T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429758 | ||||||
chr10:45429767
|
T | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(151): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.981+1003T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429767 | ||||||
chr10:45429816
|
G | A | 1 | a0001c0006t0009g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.981+1052G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45429816 | ||||||
chr10:45430054
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.981+1290G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430054 | ||||||
chr10:45430116
|
G | C | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.981+1352G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430116 | ||||||
chr10:45430141
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.981+1377A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430141 | ||||||
chr10:45430218
|
T | C | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+1454T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430218 | ||||||
chr10:45430358
|
C | A | 1 | a0001c0002t0002g0277 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.981+1594C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430358 | ||||||
chr10:45430428
|
GA | G | 12 | a0001c0001t0001g0220a0001c0001t0004g0203a0001c0002t0007g0307others(9): Show | 12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.981+1674delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45430428 | |||||
chr10:45430631
|
TA | T | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+1879delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45430631 | |||||
chr10:45430777
|
G | A | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+2013G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45430777 | ||||||
chr10:45430796
|
CACAGCGA others(26): Show |
C | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | NA18961.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.981+2038_981+2070d others(35): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45430796 | |||||
chr10:45431452
|
G | A | 1 | a0001c0006t0009g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.981+2688G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431452 | ||||||
chr10:45431548
|
G | GTTAT | 21 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0088others(18): Show | 22 | HG01109.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.981+2823_981+2826d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | |||||
chr10:45431548
|
G | GTTATTTA others(1): Show |
5 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0001t0001g0186others(2): Show | 5 | NA18955.hp1 NA18956.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+2819_981+2826d others(10): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | |||||
chr10:45431548
|
GTTAT | G | 36 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0043others(33): Show | 41 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.981+2823_981+2826d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | |||||
chr10:45431548
|
GTTATTTA others(1): Show |
G | 15 | a0001c0001t0001g0021a0001c0001t0001g0192a0001c0001t0001g0209others(12): Show | 17 | HG01243.hp1 HG01261.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.981+2819_981+2826d others(10): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | |||||
chr10:45431548
|
GTTATTTA others(5): Show |
G | 2 | a0001c0004t0001g0068a0001c0004t0001g0176 | 2 | HG03225.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.981+2815_981+2826d others(14): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | |||||
chr10:45431548
|
GTTATTTA others(9): Show |
G | 2 | a0001c0006t0001g0034a0001c0008t0002g0259 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.981+2811_981+2826d others(18): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | |||||
chr10:45431548
|
GTTATTTA others(13): Show |
G | 17 | a0001c0006t0001g0144a0002c0005t0003g0036a0002c0005t0003g0039others(14): Show | 17 | HG01243.hp2 HG02040.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.981+2807_981+2826d others(22): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45431548 | |||||
chr10:45431588
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0093a0001c0001t0001g0094 | 3 | HG01891.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.981+2824T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431588 | ||||||
chr10:45431627
|
C | T | 1 | a0001c0003t0001g0056 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.981+2863C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431627 | ||||||
chr10:45431666
|
A | G | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+2902A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431666 | ||||||
chr10:45431682
|
C | T | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+2918C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431682 | ||||||
chr10:45431794
|
G | A | 21 | a0001c0001t0001g0194a0001c0001t0001g0254a0001c0003t0001g0056others(18): Show | 25 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.981+3030G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431794 | ||||||
chr10:45431861
|
C | T | 12 | a0001c0001t0001g0167a0001c0004t0001g0007a0001c0004t0001g0008others(9): Show | 16 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.981+3097C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431861 | ||||||
chr10:45431868
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.981+3104G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45431868 | ||||||
chr10:45432027
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0209 | 2 | NA19056.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.981+3263G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432027 | ||||||
chr10:45432028
|
TG | T | 5 | a0001c0002t0002g0310a0001c0002t0002g0311a0001c0003t0001g0016others(2): Show | 7 | HG01243.hp1 HG02572.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.981+3269delG | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45432028 | |||||
chr10:45432187
|
TA | T | 6 | a0001c0001t0001g0223a0001c0001t0001g0244a0001c0001t0008g0255others(3): Show | 6 | HG01891.hp2 HG03239.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.981+3437delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45432187 | |||||
chr10:45432187
|
TAA | T | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+3436_981+3437d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45432187 | |||||
chr10:45432341
|
C | G | 28 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(25): Show | 28 | HG01243.hp2 HG01261.hp2 HG01928.hp2 others(25): Show |
intron_variant | MODIFIER | c.981+3577C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432341 | ||||||
chr10:45432343
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.981+3579G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432343 | ||||||
chr10:45432360
|
TA | T | 14 | a0001c0001t0001g0086a0001c0001t0001g0106a0001c0001t0001g0169others(11): Show | 14 | HG00741.hp1 HG01069.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.981+3613delA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45432360 | |||||
chr10:45432697
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.981+3933G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432697 | ||||||
chr10:45432747
|
A | G | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+3983A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432747 | ||||||
chr10:45432754
|
C | T | 6 | a0001c0001t0001g0167a0001c0004t0001g0008a0001c0004t0001g0028others(3): Show | 8 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+3990C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432754 | ||||||
chr10:45432785
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0171a0001c0001t0001g0195others(4): Show | 8 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+4021G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432785 | ||||||
chr10:45432813
|
T | A | 6 | a0001c0001t0001g0194a0001c0004t0001g0002a0001c0004t0001g0129others(3): Show | 8 | HG00140.hp1 NA18941.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+4049T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432813 | ||||||
chr10:45432943
|
T | A | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+4179T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432943 | ||||||
chr10:45432944
|
C | A | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+4180C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432944 | ||||||
chr10:45432974
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.981+4210C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432974 | ||||||
chr10:45432981
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.981+4217A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45432981 | ||||||
chr10:45433168
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.981+4404C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433168 | ||||||
chr10:45433210
|
T | G | 21 | a0001c0001t0001g0194a0001c0001t0001g0254a0001c0003t0001g0056others(18): Show | 25 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.981+4446T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433210 | ||||||
chr10:45433239
|
A | C | 17 | a0001c0006t0001g0144a0002c0005t0003g0036a0002c0005t0003g0039others(14): Show | 17 | HG01243.hp2 HG02040.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.981+4475A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433239 | ||||||
chr10:45433258
|
G | A | 1 | a0001c0002t0002g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.981+4494G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433258 | ||||||
chr10:45433344
|
G | A | 1 | a0001c0003t0004g0050 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.981+4580G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433344 | ||||||
chr10:45433345
|
C | T | 2 | a0001c0003t0001g0018a0001c0003t0001g0155 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.981+4581C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433345 | ||||||
chr10:45433346
|
G | A | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+4582G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433346 | ||||||
chr10:45433374
|
C | T | 42 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(39): Show | 45 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.981+4610C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433374 | ||||||
chr10:45433456
|
T | G | 28 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(25): Show | 28 | HG01243.hp2 HG01261.hp2 HG01928.hp2 others(25): Show |
intron_variant | MODIFIER | c.981+4692T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433456 | ||||||
chr10:45433463
|
C | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(221): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.981+4699C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433463 | ||||||
chr10:45433528
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.981+4764G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433528 | ||||||
chr10:45433548
|
A | T | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+4784A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433548 | ||||||
chr10:45433655
|
C | T | 1 | a0001c0002t0002g0285 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.981+4891C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433655 | ||||||
chr10:45433675
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.981+4911G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433675 | ||||||
chr10:45433785
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.981+5021C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433785 | ||||||
chr10:45433865
|
G | C | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.981+5101G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45433865 | ||||||
chr10:45434277
|
C | T | 1 | a0001c0007t0001g0130 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.981+5513C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434277 | ||||||
chr10:45434515
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.981+5751C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434515 | ||||||
chr10:45434517
|
T | C | 29 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(26): Show | 29 | HG01243.hp2 HG01261.hp2 HG01928.hp2 others(26): Show |
intron_variant | MODIFIER | c.981+5753T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434517 | ||||||
chr10:45434536
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.981+5772T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434536 | ||||||
chr10:45434693
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.982-5737G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434693 | ||||||
chr10:45434887
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.982-5543G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434887 | ||||||
chr10:45434906
|
T | TTTTC | 12 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(9): Show | 12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-5518_982-5515d others(6): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45434906 | |||||
chr10:45434938
|
G | A | 12 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(9): Show | 12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-5492G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434938 | ||||||
chr10:45434951
|
G | A | 12 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(9): Show | 12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-5479G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45434951 | ||||||
chr10:45435015
|
A | G | 1 | a0001c0002t0002g0292 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.982-5415A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435015 | ||||||
chr10:45435033
|
A | G | 12 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(9): Show | 12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-5397A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435033 | ||||||
chr10:45435049
|
T | C | 1 | a0002c0005t0003g0120 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.982-5381T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435049 | ||||||
chr10:45435262
|
G | GT | 41 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0060others(38): Show | 43 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.982-5155dupT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45435262 | |||||
chr10:45435266
|
T | TG | 2 | a0001c0001t0001g0013a0001c0001t0001g0043 | 3 | HG01070.hp1 HG01071.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.982-5164_982-5163i others(3): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435266 | ||||||
chr10:45435274
|
T | A | 1 | a0001c0006t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.982-5156T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435274 | ||||||
chr10:45435275
|
T | A | 12 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(9): Show | 12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-5155T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435275 | ||||||
chr10:45435331
|
G | T | 1 | a0001c0004t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.982-5099G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435331 | ||||||
chr10:45435337
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.982-5093T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435337 | ||||||
chr10:45435357
|
T | C | 71 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(68): Show | 74 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.982-5073T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435357 | ||||||
chr10:45435357
|
T | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0179a0001c0001t0001g0180 | 6 | NA18944.hp2 NA18947.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.982-5073T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435357 | ||||||
chr10:45435382
|
A | G | 1 | a0001c0002t0002g0289 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.982-5048A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435382 | ||||||
chr10:45435397
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.982-5033C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435397 | ||||||
chr10:45435417
|
C | A | 1 | a0001c0002t0006g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.982-5013C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435417 | ||||||
chr10:45435612
|
A | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(30): Show | 36 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.982-4818A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435612 | ||||||
chr10:45435622
|
A | G | 54 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(51): Show | 57 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.982-4808A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435622 | ||||||
chr10:45435654
|
T | C | 54 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(51): Show | 57 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.982-4776T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435654 | ||||||
chr10:45435812
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.982-4618G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435812 | ||||||
chr10:45435980
|
G | A | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-4450G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45435980 | ||||||
chr10:45436022
|
T | A | 1 | a0001c0004t0001g0028 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.982-4408T>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436022 | ||||||
chr10:45436026
|
G | A | 1 | a0009c0014t0001g0098 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.982-4404G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436026 | ||||||
chr10:45436030
|
G | A | 72 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(69): Show | 75 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.982-4400G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436030 | ||||||
chr10:45436116
|
G | T | 17 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0063others(14): Show | 19 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.982-4314G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436116 | ||||||
chr10:45436177
|
A | C | 2 | a0001c0006t0001g0142a0001c0006t0009g0153 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.982-4253A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436177 | ||||||
chr10:45436351
|
C | G | 1 | a0001c0006t0001g0034 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.982-4079C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436351 | ||||||
chr10:45436412
|
A | G | 1 | a0001c0003t0002g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.982-4018A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436412 | ||||||
chr10:45436415
|
G | A | 1 | a0001c0003t0001g0145 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.982-4015G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436415 | ||||||
chr10:45436451
|
C | T | 60 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(57): Show | 63 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.982-3979C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436451 | ||||||
chr10:45436516
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.982-3914C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436516 | ||||||
chr10:45436552
|
G | A | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-3878G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436552 | ||||||
chr10:45436552
|
G | T | 1 | a0001c0006t0001g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.982-3878G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436552 | ||||||
chr10:45436732
|
C | T | 2 | a0001c0006t0001g0142a0001c0008t0002g0259 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.982-3698C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436732 | ||||||
chr10:45436816
|
T | C | 71 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(68): Show | 74 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.982-3614T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436816 | ||||||
chr10:45436885
|
A | G | 1 | a0001c0008t0002g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.982-3545A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436885 | ||||||
chr10:45436892
|
C | G | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-3538C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45436892 | ||||||
chr10:45437001
|
C | A | 2 | a0001c0001t0001g0106a0001c0002t0002g0266 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.982-3429C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437001 | ||||||
chr10:45437090
|
C | T | 1 | a0002c0005t0003g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.982-3340C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437090 | ||||||
chr10:45437214
|
G | A | 1 | a0001c0002t0006g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.982-3216G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437214 | ||||||
chr10:45437416
|
G | GT | 12 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(9): Show | 12 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.982-3004dupT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45437416 | |||||
chr10:45437471
|
G | C | 18 | a0001c0001t0001g0089a0001c0001t0001g0199a0001c0002t0002g0025others(15): Show | 19 | HG02027.hp2 HG02132.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.982-2959G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437471 | ||||||
chr10:45437703
|
T | C | 1 | a0001c0019t0001g0213 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.982-2727T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437703 | ||||||
chr10:45437757
|
C | T | 9 | a0001c0001t0001g0069a0001c0001t0001g0164a0001c0001t0002g0305others(6): Show | 9 | HG01099.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.982-2673C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437757 | ||||||
chr10:45437890
|
C | T | 7 | a0001c0001t0001g0164a0001c0003t0001g0143a0001c0003t0001g0145others(4): Show | 7 | HG01099.hp1 HG02258.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.982-2540C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45437890 | ||||||
chr10:45438129
|
CT | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(250): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.982-2288delT | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45438129 | |||||
chr10:45438291
|
A | G | 2 | a0001c0006t0001g0142a0001c0006t0009g0153 | 2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.982-2139A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438291 | ||||||
chr10:45438378
|
G | A | 1 | a0001c0003t0001g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.982-2052G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438378 | ||||||
chr10:45438394
|
T | C | 1 | a0001c0006t0001g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.982-2036T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438394 | ||||||
chr10:45438431
|
A | T | 1 | a0001c0007t0001g0108 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.982-1999A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438431 | ||||||
chr10:45438485
|
GTCAGGAA others(21): Show |
G | 60 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(57): Show | 63 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.982-1901_982-1874d others(30): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 45438485 | |||||
chr10:45438710
|
C | T | 1 | a0001c0002t0002g0292 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.982-1720C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438710 | ||||||
chr10:45438794
|
A | G | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-1636A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438794 | ||||||
chr10:45438863
|
C | G | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-1567C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438863 | ||||||
chr10:45438883
|
C | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(151): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.982-1547C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438883 | ||||||
chr10:45438890
|
C | A | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.982-1540C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438890 | ||||||
chr10:45438924
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(151): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.982-1506G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438924 | ||||||
chr10:45438989
|
G | A | 49 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(46): Show | 52 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.982-1441G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45438989 | ||||||
chr10:45439070
|
A | C | 1 | a0001c0006t0001g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.982-1360A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439070 | ||||||
chr10:45439081
|
T | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(151): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.982-1349T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439081 | ||||||
chr10:45439347
|
G | A | 48 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(45): Show | 51 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.982-1083G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439347 | ||||||
chr10:45439433
|
C | A | 58 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(55): Show | 61 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.982-997C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439433 | ||||||
chr10:45439474
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.982-956C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439474 | ||||||
chr10:45439518
|
C | T | 7 | a0001c0001t0001g0164a0001c0003t0001g0143a0001c0003t0001g0145others(4): Show | 7 | HG01099.hp1 HG02258.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.982-912C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439518 | ||||||
chr10:45439613
|
G | A | 1 | a0001c0002t0002g0280 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.982-817G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45439613 | ||||||
chr10:45440028
|
A | C | 1 | a0001c0008t0002g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.982-402A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45440028 | ||||||
chr10:45440077
|
G | A | 1 | a0001c0006t0009g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.982-353G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45440077 | ||||||
chr10:45440101
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0220 | 2 | NA18747.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.982-329G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45440101 | ||||||
chr10:45440115
|
G | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(222): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.982-315G>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45440115 | ||||||
chr10:45440296
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(151): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.982-134C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 7/13 | chr10 | 45440296 | ||||||
chr10:45440648
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1185+15C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45440648 | ||||||
chr10:45440715
|
G | GA | 12 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0106others(9): Show | 13 | HG00642.hp2 HG01069.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1185+83dupA | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 45440715 | |||||
chr10:45440776
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(210): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.1185+143A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45440776 | ||||||
chr10:45440878
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1185+245T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45440878 | ||||||
chr10:45440911
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(209): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.1185+278G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45440911 | ||||||
chr10:45440958
|
C | T | 1 | a0001c0007t0001g0131 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1185+325C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45440958 | ||||||
chr10:45441020
|
T | C | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1186-324T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45441020 | ||||||
chr10:45441186
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0189a0001c0001t0001g0190others(1): Show | 4 | HG01070.hp2 HG01261.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186-158G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45441186 | ||||||
chr10:45441250
|
A | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0100 | 2 | HG00323.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1186-94A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45441250 | ||||||
chr10:45441277
|
C | T | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1186-67C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 8/13 | chr10 | 45441277 | ||||||
chr10:45441479
|
C | T | 1 | a0001c0008t0002g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1272+49C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441479 | ||||||
chr10:45441489
|
C | A | 1 | a0001c0001t0001g0240 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1272+59C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441489 | ||||||
chr10:45441510
|
C | G | 11 | a0001c0001t0004g0203a0001c0002t0007g0307a0001c0002t0007g0308others(8): Show | 11 | HG01261.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1272+80C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441510 | ||||||
chr10:45441625
|
C | A | 1 | a0001c0007t0001g0108 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1272+195C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441625 | ||||||
chr10:45441626
|
A | C | 1 | a0001c0007t0001g0108 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1272+196A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441626 | ||||||
chr10:45441627
|
C | A | 1 | a0001c0007t0001g0108 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1272+197C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441627 | ||||||
chr10:45441711
|
C | A | 1 | a0001c0001t0001g0184 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1272+281C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441711 | ||||||
chr10:45441750
|
A | G | 1 | a0001c0004t0001g0014 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1272+320A>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441750 | ||||||
chr10:45441751
|
C | T | 1 | a0001c0008t0002g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1272+321C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441751 | ||||||
chr10:45441975
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(160): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1272+545C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45441975 | ||||||
chr10:45442019
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0216 | 2 | NA18946.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1272+589G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442019 | ||||||
chr10:45442030
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1272+600T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442030 | ||||||
chr10:45442130
|
C | T | 5 | a0001c0003t0001g0033a0001c0004t0001g0007a0001c0004t0001g0014others(2): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272+700C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442130 | ||||||
chr10:45442280
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1273-758T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442280 | ||||||
chr10:45442409
|
C | A | 1 | a0001c0004t0001g0090 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1273-629C>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442409 | ||||||
chr10:45442459
|
C | T | 5 | a0001c0004t0001g0008a0001c0004t0001g0028a0001c0004t0001g0038others(2): Show | 7 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1273-579C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442459 | ||||||
chr10:45442466
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1273-572G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442466 | ||||||
chr10:45442477
|
A | ATG | 4 | a0001c0001t0001g0178a0001c0001t0001g0189a0001c0001t0001g0190others(1): Show | 4 | HG01070.hp2 HG01261.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273-550_1273-549d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 45442477 | |||||
chr10:45442538
|
A | T | 3 | a0001c0001t0001g0063a0001c0003t0001g0154a0001c0003t0001g0163 | 3 | HG03486.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1273-500A>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442538 | ||||||
chr10:45442544
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(179): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1273-494A>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442544 | ||||||
chr10:45442647
|
CTG | C | 45 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0046others(42): Show | 47 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1273-390_1273-389d others(4): Show |
ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442647 | ||||||
chr10:45442791
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(207): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1273-247T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442791 | ||||||
chr10:45442799
|
T | G | 52 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0089others(49): Show | 55 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1273-239T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442799 | ||||||
chr10:45442827
|
T | C | 1 | a0001c0004t0001g0008 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1273-211T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442827 | ||||||
chr10:45442831
|
T | C | 1 | a0001c0006t0001g0034 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1273-207T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442831 | ||||||
chr10:45442853
|
G | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(206): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1273-185G>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 9/13 | chr10 | 45442853 | ||||||
chr10:45443229
|
G | A | 3 | a0001c0002t0002g0027a0001c0002t0002g0293a0001c0002t0002g0294 | 4 | HG00323.hp2 HG01175.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451+13G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 10/13 | chr10 | 45443229 | ||||||
chr10:45443239
|
T | C | 4 | a0001c0002t0002g0310a0001c0002t0002g0311a0001c0003t0001g0016others(1): Show | 5 | HG01243.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1451+23T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 10/13 | chr10 | 45443239 | ||||||
chr10:45443298
|
C | T | 51 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0046others(48): Show | 53 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1451+82C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 10/13 | chr10 | 45443298 | ||||||
chr10:45443553
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1573+16C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 11/13 | chr10 | 45443553 | ||||||
chr10:45443559
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1573+22C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 11/13 | chr10 | 45443559 | ||||||
chr10:45443631
|
C | T | 5 | a0001c0004t0001g0008a0001c0004t0001g0028a0001c0004t0001g0038others(2): Show | 7 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573+94C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 11/13 | chr10 | 45443631 | ||||||
chr10:45443688
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.1574-40T>C | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 11/13 | chr10 | 45443688 | ||||||
chr10:45443889
|
G | A | 2 | a0001c0003t0001g0006a0001c0003t0001g0032 | 3 | HG03453.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1674+61G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 12/13 | chr10 | 45443889 | ||||||
chr10:45444370
|
C | T | 34 | a0001c0004t0001g0002a0001c0004t0001g0007a0001c0004t0001g0008others(31): Show | 42 | HG00280.hp2 HG00408.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1845+84C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45444370 | ||||||
chr10:45444533
|
T | G | 6 | a0002c0005t0003g0036a0002c0005t0003g0113a0002c0005t0003g0122others(3): Show | 6 | HG02040.hp1 HG02155.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1845+247T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45444533 | ||||||
chr10:45444543
|
C | T | 46 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0046others(43): Show | 48 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.1845+257C>T | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45444543 | ||||||
chr10:45444728
|
G | A | 1 | a0001c0007t0001g0124 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1845+442G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45444728 | ||||||
chr10:45444827
|
T | G | 3 | a0001c0004t0001g0007a0001c0004t0001g0064a0001c0004t0001g0065 | 4 | HG02258.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845+541T>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45444827 | ||||||
chr10:45445142
|
C | G | 1 | a0001c0006t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1846-366C>G | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45445142 | ||||||
chr10:45445174
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1846-334G>A | ALOX5 | ENSG00000012779.12 | transcript | ENST00000374391.7 | protein_coding | 13/13 | chr10 | 45445174 |