geneid | 7453 |
---|---|
ensemblid | ENSG00000140105.18 |
hgncid | 12729 |
symbol | WARS1 |
name | tryptophanyl-tRNA synthetase 1 |
refseq_nuc | NM_004184.4 |
refseq_prot | NP_004175.2 |
ensembl_nuc | ENST00000392882.7 |
ensembl_prot | ENSP00000376620.2 |
mane_status | MANE Select |
chr | chr14 |
start | 100333790 |
end | 100375347 |
strand | - |
ver | v1.2 |
region | chr14:100333790-100375347 |
region5000 | chr14:100328790-100380347 |
regionname0 | WARS1_chr14_100333790_100375347 |
regionname5000 | WARS1_chr14_100328790_100380347 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 471 | 331 | 95 | 46 | 144 | 14 | 30 | 110 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0002 | 0/0 | 471 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0003 | 0/0 | 471 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
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 | 1416 | 200 | 43 | 36 | 87 | 9 | 24 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
c0002 | 1/0 | 1416 | 126 | 51 | 9 | 56 | 5 | 4 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
c0003 | 0/0 | 1416 | 4 | 0 | 0 | 4 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
c0004 | 0/0 | 1416 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
c0005 | 0/0 | 1416 | 2 | 0 | 0 | 0 | 0 | 2 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
c0006 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
c0007 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
c0008 | 0/0 | 1416 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
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 | 1/1 | 1224 | 303 | 97 | 46 | 115 | 13 | 30 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
t0002 | 0/0 | 1224 | 33 | 0 | 0 | 32 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
t0003 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
t0004 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
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 | 6 | 3 | 1 | 0 | 2 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0004 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
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 | 1416 | 200 | 43 | 36 | 87 | 9 | 24 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0002 | 1/0 | 1416 | 126 | 51 | 9 | 56 | 5 | 4 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0005 | 0/0 | 1416 | 2 | 0 | 0 | 0 | 0 | 2 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0006 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0007 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0008 | 0/0 | 1416 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0002c0003 | 0/0 | 1416 | 4 | 0 | 0 | 4 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0003c0004 | 0/0 | 1416 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2639 | 199 | 42 | 36 | 87 | 9 | 24 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0001t0003 | 0/0 | 2639 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0002t0001 | 1/0 | 2639 | 92 | 51 | 9 | 23 | 4 | 4 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0002t0002 | 0/0 | 2639 | 33 | 0 | 0 | 32 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0002t0004 | 0/0 | 2639 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0005t0001 | 0/0 | 2639 | 2 | 0 | 0 | 0 | 0 | 2 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0006t0001 | 0/0 | 2639 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0007t0001 | 0/0 | 2639 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0001c0008t0001 | 0/0 | 2639 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0002c0003t0001 | 0/0 | 2639 | 4 | 0 | 0 | 4 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
a0003c0004t0001 | 0/0 | 2639 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | copy fasta | chr14 | 100328790 | 100380347 |
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 | 6 | 3 | 1 | 0 | 2 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0005t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0005t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0006t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0007t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0001c0008t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
a0003c0004t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0034 | EUR | GBR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0065 | EUR | GBR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0066 | EUR | FIN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | FIN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00558 | hp1 | a0001 | c0002 | t0004 | g0082 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0072 | EUR | IBS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0075 | EUR | IBS | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CDX | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CDX | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | CDX | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02293 | hp1 | a0001 | c0006 | t0001 | g0189 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02451 | hp2 | a0001 | c0007 | t0001 | g0048 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02723 | hp1 | a0003 | c0004 | t0001 | g0006 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03486 | hp2 | a0003 | c0004 | t0001 | g0006 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | GWD | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03942 | hp2 | a0001 | c0005 | t0001 | g0291 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG04115 | hp1 | a0001 | c0005 | t0001 | g0290 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | STU | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | CHB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0110 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18973 | hp2 | a0002 | c0003 | t0001 | g0125 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18978 | hp2 | a0001 | c0008 | t0001 | g0201 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18985 | hp2 | a0002 | c0003 | t0001 | g0124 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18997 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0127 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19088 | hp1 | a0002 | c0003 | t0001 | g0126 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | ASW | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | GIH | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02109 | hp1 | a0003 | c0004 | t0001 | g0006 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | USA | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | USA | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | USA | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | USA | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | LWK | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0179 | REF | REF | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0113 | REF | REF | WARS1_chr14_100328790_100380347 | WARS1 | chr14 | 100328790 | 100380347 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100342522
|
G | A | 1 | a0003 | 3 | HG02109.hp1 HG02723.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.989C>T | p.Pro330Leu | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/11 | 1127/2639 | 989/1416 | 330/471 | chr14 | 100342522 | ||
chr14:100361861
|
C | A | 1 | a0002 | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
missense_variant | MODERATE | c.160G>T | p.Ala54Ser | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/11 | 298/2639 | 160/1416 | 54/471 | chr14 | 100361861 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100337086
|
G | A | 1 | a0001c0005 | 2 | HG03942.hp2 HG04115.hp1 |
synonymous_variant | LOW | c.1230C>T | p.Asp410Asp | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/11 | 1368/2639 | 1230/1416 | 410/471 | chr14 | 100337086 | ||
chr14:100342508
|
G | A | 3 | a0001c0001a0001c0006a0001c0008 | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
synonymous_variant | LOW | c.1003C>T | p.Leu335Leu | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/11 | 1141/2639 | 1003/1416 | 335/471 | chr14 | 100342508 | ||
chr14:100346771
|
G | A | 1 | a0001c0007 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.801C>T | p.Phe267Phe | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/11 | 939/2639 | 801/1416 | 267/471 | chr14 | 100346771 | ||
chr14:100353719
|
C | T | 1 | a0001c0006 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.693G>A | p.Lys231Lys | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/11 | 831/2639 | 693/1416 | 231/471 | chr14 | 100353719 | ||
chr14:100361721
|
G | A | 1 | a0001c0008 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.300C>T | p.Tyr100Tyr | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/11 | 438/2639 | 300/1416 | 100/471 | chr14 | 100361721 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100334273
|
T | C | 1 | a0001c0002t0002 | 33 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*602A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 602 | chr14 | 100334273 | |||||
chr14:100334376
|
G | C | 1 | a0001c0001t0003 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*499C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 499 | chr14 | 100334376 | |||||
chr14:100334378
|
G | A | 1 | a0001c0001t0003 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*497C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 497 | chr14 | 100334378 | |||||
chr14:100334379
|
G | A | 1 | a0001c0001t0003 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*496C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 496 | chr14 | 100334379 | |||||
chr14:100334380
|
G | A | 1 | a0001c0001t0003 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 495 | chr14 | 100334380 | |||||
chr14:100334662
|
G | A | 1 | a0001c0002t0004 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*213C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 11/11 | 213 | chr14 | 100334662 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100335047
|
G | A | 6 | a0001c0002t0001g0013a0001c0002t0001g0069a0001c0002t0001g0076others(3): Show | 7 | HG00544.hp1 HG03491.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.1255-11C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335047 | ||||||
chr14:100335086
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1255-50A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335086 | ||||||
chr14:100335087
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1255-51C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335087 | ||||||
chr14:100335092
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1255-56G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335092 | ||||||
chr14:100335106
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1255-70G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335106 | ||||||
chr14:100335164
|
G | C | 30 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(27): Show | 37 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(34): Show |
intron_variant | MODIFIER | c.1255-128C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335164 | ||||||
chr14:100335207
|
A | G | 10 | a0001c0002t0001g0018a0001c0002t0001g0115a0001c0002t0001g0116others(7): Show | 11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1255-171T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335207 | ||||||
chr14:100335361
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0228 | 2 | NA19074.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1255-325A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335361 | ||||||
chr14:100335383
|
A | AT | 79 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0140others(76): Show | 83 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1255-348dupA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335383 | ||||||
chr14:100335733
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1255-697C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335733 | ||||||
chr14:100335757
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1255-721G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335757 | ||||||
chr14:100335871
|
T | C | 2 | a0001c0002t0001g0033a0001c0007t0001g0048 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1255-835A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335871 | ||||||
chr14:100335940
|
G | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1255-904C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335940 | ||||||
chr14:100335964
|
C | CT | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0212others(3): Show | 6 | HG01928.hp1 HG01975.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-929dupA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335964 | ||||||
chr14:100335964
|
CT | C | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0195others(4): Show | 7 | HG00558.hp1 HG01496.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255-929delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100335964 | ||||||
chr14:100336071
|
C | T | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1254+991G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336071 | ||||||
chr14:100336092
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1254+970C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336092 | ||||||
chr14:100336148
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1254+914A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336148 | ||||||
chr14:100336149
|
G | T | 10 | a0001c0002t0001g0018a0001c0002t0001g0115a0001c0002t0001g0116others(7): Show | 11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1254+913C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336149 | ||||||
chr14:100336168
|
C | T | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1254+894G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336168 | ||||||
chr14:100336275
|
C | CA | 13 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0057others(10): Show | 15 | HG00733.hp2 HG02055.hp1 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.1254+786dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336275 | ||||||
chr14:100336275
|
C | CAAA | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 196 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.1254+784_1254+786d others(5): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336275 | ||||||
chr14:100336536
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1254+526A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336536 | ||||||
chr14:100336691
|
T | C | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+371A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336691 | ||||||
chr14:100336851
|
T | C | 6 | a0001c0002t0001g0017a0001c0002t0001g0100a0001c0002t0001g0101others(3): Show | 7 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1254+211A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336851 | ||||||
chr14:100336953
|
T | C | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+109A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336953 | ||||||
chr14:100336961
|
T | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1254+101A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100336961 | ||||||
chr14:100337027
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1254+35T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 10/10 | chr14 | 100337027 | ||||||
chr14:100337278
|
T | A | 1 | a0001c0002t0001g0077 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1114-76A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337278 | ||||||
chr14:100337318
|
C | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1114-116G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337318 | ||||||
chr14:100337345
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1114-143A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337345 | ||||||
chr14:100337345
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1114-143A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337345 | ||||||
chr14:100337405
|
C | G | 44 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(41): Show | 50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1114-203G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337405 | ||||||
chr14:100337619
|
G | C | 1 | a0001c0002t0001g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1114-417C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337619 | ||||||
chr14:100337620
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1114-418C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337620 | ||||||
chr14:100337688
|
C | CA | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1114-487dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337688 | ||||||
chr14:100337727
|
G | T | 1 | a0001c0002t0001g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1114-525C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337727 | ||||||
chr14:100337732
|
C | T | 2 | a0001c0002t0002g0035a0001c0002t0002g0036 | 2 | HG02165.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1114-530G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337732 | ||||||
chr14:100337801
|
T | C | 6 | a0001c0002t0001g0007a0001c0002t0001g0107a0001c0002t0001g0109others(3): Show | 8 | HG02559.hp2 HG02717.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114-599A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337801 | ||||||
chr14:100337881
|
T | C | 8 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(5): Show | 8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114-679A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337881 | ||||||
chr14:100337978
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1114-776A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100337978 | ||||||
chr14:100338017
|
A | G | 1 | a0001c0001t0001g0020 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1114-815T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338017 | ||||||
chr14:100338058
|
C | T | 1 | a0001c0002t0001g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1114-856G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338058 | ||||||
chr14:100338207
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1114-1005G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338207 | ||||||
chr14:100338256
|
G | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1114-1054C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338256 | ||||||
chr14:100338412
|
T | G | 2 | a0001c0002t0001g0065a0001c0002t0001g0075 | 2 | HG00140.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1114-1210A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338412 | ||||||
chr14:100338448
|
G | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0019others(78): Show | 87 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.1114-1246C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338448 | ||||||
chr14:100338776
|
A | C | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-1574T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338776 | ||||||
chr14:100338849
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1114-1647C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338849 | ||||||
chr14:100338935
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1114-1733G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338935 | ||||||
chr14:100338949
|
C | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1114-1747G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338949 | ||||||
chr14:100338966
|
C | T | 1 | a0001c0008t0001g0201 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1114-1764G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338966 | ||||||
chr14:100338982
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0221a0001c0001t0001g0222others(5): Show | 11 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1114-1780A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100338982 | ||||||
chr14:100339088
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1114-1886T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339088 | ||||||
chr14:100339103
|
T | TCA | 43 | a0001c0002t0001g0007a0001c0002t0001g0017a0001c0002t0001g0033others(40): Show | 53 | HG00099.hp1 HG00423.hp1 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.1114-1903_1114-190 others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339103 | ||||||
chr14:100339103
|
T | TCACA | 5 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0120others(2): Show | 6 | HG02622.hp1 HG03041.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-1905_1114-190 others(8): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339103 | ||||||
chr14:100339108
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0001g0020 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1114-1922_1114-190 others(20): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339108 | ||||||
chr14:100339120
|
C | CACACAT | 10 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(7): Show | 11 | HG02280.hp1 HG02572.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114-1919_1114-191 others(10): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339120 | ||||||
chr14:100339122
|
C | CACACACA others(1): Show |
4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-1921_1114-192 others(12): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339122 | ||||||
chr14:100339122
|
CAT | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1114-1922_1114-192 others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339122 | ||||||
chr14:100339124
|
T | C | 77 | a0001c0001t0001g0173a0001c0001t0001g0187a0001c0001t0001g0267others(74): Show | 85 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1114-1922A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339124 | ||||||
chr14:100339126
|
C | CAT | 43 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(40): Show | 49 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1114-1925_1114-192 others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339126 | ||||||
chr14:100339126
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG01069.hp2 HG01981.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-1924G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339126 | ||||||
chr14:100339128
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1114-1926G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339128 | ||||||
chr14:100339130
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1114-1928G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339130 | ||||||
chr14:100339246
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1114-2044A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339246 | ||||||
chr14:100339282
|
C | T | 2 | a0001c0001t0001g0194a0001c0002t0001g0088 | 2 | HG01169.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1114-2080G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339282 | ||||||
chr14:100339358
|
A | G | 9 | a0001c0002t0001g0018a0001c0002t0001g0114a0001c0002t0001g0117others(6): Show | 10 | HG00639.hp1 HG01884.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1114-2156T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339358 | ||||||
chr14:100339367
|
A | G | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-2165T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339367 | ||||||
chr14:100339371
|
T | C | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-2169A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339371 | ||||||
chr14:100339388
|
A | G | 3 | a0001c0001t0001g0025a0001c0002t0002g0035a0001c0002t0002g0036 | 3 | HG01928.hp1 HG02165.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1114-2186T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339388 | ||||||
chr14:100339415
|
C | T | 4 | a0001c0001t0001g0108a0001c0001t0001g0208a0001c0001t0001g0270others(1): Show | 4 | HG01099.hp2 HG02257.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-2213G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339415 | ||||||
chr14:100339418
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02257.hp1 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1114-2216G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339418 | ||||||
chr14:100339427
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1114-2225G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339427 | ||||||
chr14:100339450
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1114-2248A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339450 | ||||||
chr14:100339457
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 118 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1114-2255C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339457 | ||||||
chr14:100339458
|
T | C | 4 | a0001c0002t0001g0057a0001c0002t0001g0059a0001c0002t0001g0060others(1): Show | 4 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-2256A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339458 | ||||||
chr14:100339463
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1114-2261C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339463 | ||||||
chr14:100339490
|
T | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(72): Show | 78 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1114-2288A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339490 | ||||||
chr14:100339506
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1114-2304C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339506 | ||||||
chr14:100339553
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1114-2351A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339553 | ||||||
chr14:100339582
|
C | A | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1114-2380G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339582 | ||||||
chr14:100339590
|
C | CA | 26 | a0001c0001t0001g0108a0001c0001t0001g0179a0001c0001t0001g0270others(23): Show | 26 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.1114-2389dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339590 | ||||||
chr14:100339590
|
C | CAA | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1114-2390_1114-238 others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339590 | ||||||
chr14:100339590
|
C | CAAA | 31 | a0001c0001t0001g0023a0001c0001t0001g0130a0001c0001t0001g0134others(28): Show | 32 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1114-2391_1114-238 others(7): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339590 | ||||||
chr14:100339611
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1114-2409C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339611 | ||||||
chr14:100339640
|
T | C | 76 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(73): Show | 79 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1114-2438A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339640 | ||||||
chr14:100339849
|
C | T | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+2549G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100339849 | ||||||
chr14:100340045
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1113+2353A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340045 | ||||||
chr14:100340282
|
G | A | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1113+2116C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340282 | ||||||
chr14:100340313
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1113+2085C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340313 | ||||||
chr14:100340339
|
C | G | 1 | a0001c0002t0001g0119 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1113+2059G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340339 | ||||||
chr14:100340618
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1113+1780G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340618 | ||||||
chr14:100340642
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1113+1756G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340642 | ||||||
chr14:100340755
|
C | T | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1113+1643G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340755 | ||||||
chr14:100340756
|
G | A | 3 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0064 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1113+1642C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340756 | ||||||
chr14:100340799
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1113+1599C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340799 | ||||||
chr14:100340917
|
C | CT | 100 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(97): Show | 110 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1113+1480dupA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340917 | ||||||
chr14:100340936
|
C | T | 44 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(41): Show | 50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1113+1462G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340936 | ||||||
chr14:100340981
|
C | G | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+1417G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340981 | ||||||
chr14:100340986
|
C | T | 3 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0064 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1113+1412G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100340986 | ||||||
chr14:100341107
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1113+1291T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341107 | ||||||
chr14:100341130
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1113+1268C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341130 | ||||||
chr14:100341205
|
C | T | 6 | a0001c0002t0001g0007a0001c0002t0001g0107a0001c0002t0001g0109others(3): Show | 8 | HG02559.hp2 HG02717.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+1193G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341205 | ||||||
chr14:100341604
|
A | G | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+794T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341604 | ||||||
chr14:100341677
|
T | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1113+721A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341677 | ||||||
chr14:100341811
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01884.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1113+587C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341811 | ||||||
chr14:100341818
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(217): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1113+580C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341818 | ||||||
chr14:100341831
|
C | T | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.1113+567G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341831 | ||||||
chr14:100341928
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1113+470A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100341928 | ||||||
chr14:100342156
|
G | GA | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1113+241dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100342156 | ||||||
chr14:100342173
|
T | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1113+225A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100342173 | ||||||
chr14:100342228
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0136 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1113+170C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100342228 | ||||||
chr14:100342271
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1113+127C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100342271 | ||||||
chr14:100342317
|
C | T | 2 | a0001c0002t0001g0033a0001c0007t0001g0048 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1113+81G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 9/10 | chr14 | 100342317 | ||||||
chr14:100342591
|
C | G | 2 | a0001c0002t0001g0109a0001c0002t0001g0112 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.940-20G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100342591 | ||||||
chr14:100342706
|
C | CAT | 283 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(280): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.940-137_940-136dup others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100342706 | ||||||
chr14:100342715
|
CT | C | 8 | a0001c0001t0001g0194a0001c0002t0001g0017a0001c0002t0001g0060others(5): Show | 9 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.940-145delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100342715 | ||||||
chr14:100342728
|
A | T | 42 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(39): Show | 50 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.940-157T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100342728 | ||||||
chr14:100342947
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(286): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.939+328T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100342947 | ||||||
chr14:100343022
|
G | A | 1 | a0001c0002t0001g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.939+253C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100343022 | ||||||
chr14:100343088
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.939+187C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100343088 | ||||||
chr14:100343156
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.939+119G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100343156 | ||||||
chr14:100343230
|
G | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.939+45C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 8/10 | chr14 | 100343230 | ||||||
chr14:100343542
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.827-155A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343542 | ||||||
chr14:100343564
|
C | T | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.827-177G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343564 | ||||||
chr14:100343606
|
T | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG02109.hp2 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.827-219A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343606 | ||||||
chr14:100343700
|
G | T | 1 | a0001c0002t0004g0082 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.827-313C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343700 | ||||||
chr14:100343745
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.827-358G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343745 | ||||||
chr14:100343762
|
C | T | 44 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(41): Show | 50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.827-375G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343762 | ||||||
chr14:100343912
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.827-525G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100343912 | ||||||
chr14:100344059
|
GCTTCCCT | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.827-679_827-673del others(7): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344059 | ||||||
chr14:100344089
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.827-702C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344089 | ||||||
chr14:100344114
|
G | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.827-727C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344114 | ||||||
chr14:100344192
|
C | G | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.827-805G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344192 | ||||||
chr14:100344218
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(295): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.827-831T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344218 | ||||||
chr14:100344256
|
G | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.827-869C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344256 | ||||||
chr14:100344380
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.827-993A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344380 | ||||||
chr14:100344409
|
C | T | 1 | a0001c0002t0001g0083 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.827-1022G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344409 | ||||||
chr14:100344424
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.827-1037C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344424 | ||||||
chr14:100344508
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.827-1121C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344508 | ||||||
chr14:100344526
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.827-1139C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344526 | ||||||
chr14:100344547
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.827-1160C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344547 | ||||||
chr14:100344556
|
G | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.827-1169C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344556 | ||||||
chr14:100344590
|
AAAGTGAG others(33): Show |
A | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-1243_827-1204d others(42): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344590 | ||||||
chr14:100344602
|
G | A | 1 | a0001c0002t0002g0031 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.827-1215C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344602 | ||||||
chr14:100344603
|
TCTCTGCC others(33): Show |
T | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0212others(1): Show | 4 | HG01928.hp1 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-1256_827-1217d others(42): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344603 | ||||||
chr14:100344682
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.827-1295C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344682 | ||||||
chr14:100344684
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.827-1297G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344684 | ||||||
chr14:100344748
|
TGTGAGGA others(33): Show |
T | 1 | a0001c0008t0001g0201 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.827-1401_827-1362d others(42): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344748 | ||||||
chr14:100344758
|
G | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.827-1371C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344758 | ||||||
chr14:100344766
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.827-1379G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344766 | ||||||
chr14:100344783
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.827-1396G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344783 | ||||||
chr14:100344851
|
C | T | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.827-1464G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344851 | ||||||
chr14:100344880
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.827-1493T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344880 | ||||||
chr14:100344883
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.827-1496G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344883 | ||||||
chr14:100344884
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.827-1497C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344884 | ||||||
chr14:100344913
|
C | T | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.827-1526G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344913 | ||||||
chr14:100344914
|
G | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0229others(2): Show | 5 | HG00639.hp2 HG01928.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.827-1527C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344914 | ||||||
chr14:100344952
|
G | GGGGGTCA others(91): Show |
2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.827-1663_827-1566d others(100): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344952 | ||||||
chr14:100344952
|
G | GGGGGTCA others(42): Show |
4 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0176others(1): Show | 4 | HG03209.hp2 NA18946.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-1566_827-1565i others(51): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344952 | ||||||
chr14:100344970
|
C | T | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-1583G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344970 | ||||||
chr14:100344999
|
G | T | 8 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0176others(5): Show | 8 | HG03209.hp2 NA18946.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.827-1612C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100344999 | ||||||
chr14:100345019
|
C | CGGCCAGC others(42): Show |
1 | a0001c0001t0001g0183 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.827-1633_827-1632i others(51): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345019 | ||||||
chr14:100345019
|
C | T | 4 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0176others(1): Show | 4 | HG03209.hp2 NA18946.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-1632G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345019 | ||||||
chr14:100345036
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.827-1649G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345036 | ||||||
chr14:100345049
|
GC | G | 5 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0176others(2): Show | 5 | HG03209.hp2 NA18946.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-1663delG | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345049 | ||||||
chr14:100345050
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.827-1663G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345050 | ||||||
chr14:100345064
|
C | CGCCCGGC others(90): Show |
1 | a0001c0001t0001g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.827-1678_827-1677i others(99): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345064 | ||||||
chr14:100345064
|
C | CGCCCGGC others(90): Show |
175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.827-1678_827-1677i others(99): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345064 | ||||||
chr14:100345064
|
C | T | 5 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0176others(2): Show | 5 | HG03209.hp2 NA18946.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.827-1677G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345064 | ||||||
chr14:100345070
|
G | GGCCAGCC others(92): Show |
1 | a0001c0001t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.826+1675_826+1676i others(101): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345070 | ||||||
chr14:100345081
|
C | CGTCCGGG others(91): Show |
11 | a0001c0002t0001g0018a0001c0002t0001g0097a0001c0002t0001g0115others(8): Show | 12 | HG00639.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.826+1664_826+1665i others(100): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345081 | ||||||
chr14:100345081
|
C | CGTCCGGG others(92): Show |
1 | a0001c0002t0002g0042 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.826+1664_826+1665i others(101): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345081 | ||||||
chr14:100345081
|
C | CGTCCGGG others(92): Show |
1 | a0001c0002t0002g0040 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.826+1664_826+1665i others(101): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345081 | ||||||
chr14:100345081
|
C | CGTCCGGG others(91): Show |
25 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(22): Show | 32 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.826+1664_826+1665i others(100): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345081 | ||||||
chr14:100345081
|
C | CGTCCGGG others(91): Show |
1 | a0001c0002t0002g0047 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.826+1664_826+1665i others(100): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345081 | ||||||
chr14:100345113
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.826+1633G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345113 | ||||||
chr14:100345127
|
A | C | 1 | a0001c0001t0001g0178 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.826+1619T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345127 | ||||||
chr14:100345154
|
A | G | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.826+1592T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345154 | ||||||
chr14:100345170
|
G | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.826+1576C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345170 | ||||||
chr14:100345232
|
C | CG | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 105 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.826+1513dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345232 | ||||||
chr14:100345272
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.826+1474G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345272 | ||||||
chr14:100345405
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.826+1341C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345405 | ||||||
chr14:100345470
|
C | G | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+1276G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345470 | ||||||
chr14:100345484
|
A | G | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+1262T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345484 | ||||||
chr14:100345525
|
G | A | 39 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(36): Show | 47 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.826+1221C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345525 | ||||||
chr14:100345525
|
G | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 8 | HG00099.hp2 HG00738.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.826+1221C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345525 | ||||||
chr14:100345585
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.826+1161G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345585 | ||||||
chr14:100345660
|
AAAAT | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.826+1082_826+1085d others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345660 | ||||||
chr14:100345673
|
A | T | 1 | a0001c0002t0001g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.826+1073T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345673 | ||||||
chr14:100345677
|
TA | T | 10 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0079others(7): Show | 12 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.826+1068delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345677 | ||||||
chr14:100345677
|
TAA | T | 36 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(33): Show | 40 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.826+1067_826+1068d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345677 | ||||||
chr14:100345678
|
A | T | 18 | a0001c0001t0001g0019a0001c0001t0001g0168a0001c0001t0001g0192others(15): Show | 20 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.826+1068T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345678 | ||||||
chr14:100345712
|
A | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.826+1034T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345712 | ||||||
chr14:100345757
|
T | C | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.826+989A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345757 | ||||||
chr14:100345834
|
C | T | 39 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(36): Show | 47 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.826+912G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345834 | ||||||
chr14:100345848
|
C | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0094 | 3 | HG02055.hp1 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.826+898G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345848 | ||||||
chr14:100345994
|
G | A | 6 | a0001c0002t0001g0017a0001c0002t0001g0100a0001c0002t0001g0101others(3): Show | 7 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.826+752C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100345994 | ||||||
chr14:100346069
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.826+677T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346069 | ||||||
chr14:100346116
|
G | A | 4 | a0001c0002t0002g0027a0001c0002t0002g0042a0001c0002t0002g0044others(1): Show | 4 | NA18954.hp2 NA18970.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+630C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346116 | ||||||
chr14:100346166
|
GA | G | 74 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(71): Show | 77 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.826+579delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346166 | ||||||
chr14:100346168
|
A | C | 73 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(70): Show | 76 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.826+578T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346168 | ||||||
chr14:100346169
|
A | C | 73 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(70): Show | 76 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.826+577T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346169 | ||||||
chr14:100346170
|
T | C | 74 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(71): Show | 77 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.826+576A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346170 | ||||||
chr14:100346431
|
C | G | 1 | a0001c0002t0002g0043 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.826+315G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346431 | ||||||
chr14:100346450
|
A | G | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.826+296T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346450 | ||||||
chr14:100346471
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.826+275A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346471 | ||||||
chr14:100346593
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.826+153C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346593 | ||||||
chr14:100346608
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.826+138G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346608 | ||||||
chr14:100346740
|
T | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
splice_region_variant&intron_variant | LOW | c.826+6A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 7/10 | chr14 | 100346740 | ||||||
chr14:100346887
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0001g0116 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.726-41G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100346887 | ||||||
chr14:100347090
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.726-244T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347090 | ||||||
chr14:100347093
|
C | A | 3 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0284 | 3 | NA18979.hp2 NA18984.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.726-247G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347093 | ||||||
chr14:100347093
|
C | T | 15 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(12): Show | 16 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.726-247G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347093 | ||||||
chr14:100347094
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.726-248C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347094 | ||||||
chr14:100347096
|
C | T | 1 | a0001c0008t0001g0201 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.726-250G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347096 | ||||||
chr14:100347234
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.726-388A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347234 | ||||||
chr14:100347370
|
C | G | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.726-524G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347370 | ||||||
chr14:100347496
|
T | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.726-650A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347496 | ||||||
chr14:100347504
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.726-658T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347504 | ||||||
chr14:100347556
|
G | C | 8 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(5): Show | 8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.726-710C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347556 | ||||||
chr14:100347650
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.726-804G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347650 | ||||||
chr14:100347776
|
C | A | 4 | a0001c0002t0002g0010a0001c0002t0002g0030a0001c0002t0002g0040others(1): Show | 5 | NA18951.hp2 NA18956.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.726-930G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347776 | ||||||
chr14:100347777
|
A | G | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-931T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347777 | ||||||
chr14:100347867
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.726-1021C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347867 | ||||||
chr14:100347956
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.726-1110G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100347956 | ||||||
chr14:100348041
|
C | G | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.726-1195G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348041 | ||||||
chr14:100348070
|
T | C | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.726-1224A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348070 | ||||||
chr14:100348142
|
G | T | 1 | a0001c0002t0001g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.726-1296C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348142 | ||||||
chr14:100348153
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0240 | 2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.726-1307G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348153 | ||||||
chr14:100348229
|
G | C | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.726-1383C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348229 | ||||||
chr14:100348377
|
A | T | 1 | a0001c0001t0001g0211 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.726-1531T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348377 | ||||||
chr14:100348380
|
GGCA | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.726-1537_726-1535d others(5): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348380 | ||||||
chr14:100348411
|
G | T | 1 | a0001c0001t0001g0137 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.726-1565C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348411 | ||||||
chr14:100348421
|
C | T | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.726-1575G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348421 | ||||||
chr14:100348442
|
G | A | 5 | a0001c0002t0001g0017a0001c0002t0001g0101a0001c0002t0001g0102others(2): Show | 6 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.726-1596C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348442 | ||||||
chr14:100348458
|
C | T | 5 | a0001c0002t0002g0010a0001c0002t0002g0030a0001c0002t0002g0039others(2): Show | 6 | NA18951.hp2 NA18955.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.726-1612G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348458 | ||||||
chr14:100348642
|
C | T | 2 | a0001c0002t0002g0049a0001c0002t0002g0050 | 2 | HG00423.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.726-1796G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348642 | ||||||
chr14:100348809
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.726-1963T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348809 | ||||||
chr14:100348810
|
C | T | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.726-1964G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348810 | ||||||
chr14:100348964
|
T | C | 1 | a0001c0002t0001g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.726-2118A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348964 | ||||||
chr14:100348992
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.726-2146G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100348992 | ||||||
chr14:100349093
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.726-2247G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349093 | ||||||
chr14:100349181
|
T | C | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-2335A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349181 | ||||||
chr14:100349300
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.726-2454A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349300 | ||||||
chr14:100349529
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.726-2683G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349529 | ||||||
chr14:100349575
|
C | T | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.726-2729G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349575 | ||||||
chr14:100349611
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.726-2765C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100349611 | ||||||
chr14:100350103
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(295): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.726-3257T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350103 | ||||||
chr14:100350185
|
C | CAGGA | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.726-3340_726-3339i others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350185 | ||||||
chr14:100350399
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.725+3288C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350399 | ||||||
chr14:100350399
|
G | GAAAA | 14 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0166others(11): Show | 19 | HG00140.hp1 HG01074.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.725+3284_725+3287d others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350399 | ||||||
chr14:100350399
|
G | GAAAAA | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(162): Show | 181 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.725+3283_725+3287d others(7): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350399 | ||||||
chr14:100350399
|
G | GAAAAAA | 70 | a0001c0001t0001g0143a0001c0001t0001g0149a0001c0001t0001g0156others(67): Show | 81 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.725+3282_725+3287d others(8): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350399 | ||||||
chr14:100350399
|
G | GAAAAAAA | 42 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(39): Show | 46 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.725+3281_725+3287d others(9): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350399 | ||||||
chr14:100350407
|
A | G | 1 | a0001c0001t0001g0021 | 2 | NA18960.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.725+3280T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350407 | ||||||
chr14:100350464
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | HG01167.hp1 HG02040.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.725+3223C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350464 | ||||||
chr14:100350597
|
T | C | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.725+3090A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350597 | ||||||
chr14:100350627
|
G | C | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.725+3060C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350627 | ||||||
chr14:100350669
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.725+3018G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350669 | ||||||
chr14:100350688
|
T | C | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.725+2999A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350688 | ||||||
chr14:100350693
|
C | G | 2 | a0001c0002t0001g0013a0001c0002t0001g0086 | 3 | NA18950.hp1 NA19055.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.725+2994G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350693 | ||||||
chr14:100350899
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0212others(1): Show | 4 | HG01928.hp1 HG01975.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.725+2788A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350899 | ||||||
chr14:100350929
|
G | T | 16 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(13): Show | 16 | HG01433.hp2 HG02132.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.725+2758C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100350929 | ||||||
chr14:100351073
|
G | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0164 | 2 | HG02602.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.725+2614C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351073 | ||||||
chr14:100351120
|
A | T | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.725+2567T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351120 | ||||||
chr14:100351422
|
C | T | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.725+2265G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351422 | ||||||
chr14:100351477
|
A | G | 1 | a0001c0001t0001g0021 | 2 | NA18960.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.725+2210T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351477 | ||||||
chr14:100351499
|
CA | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 179 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.725+2187delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351499 | ||||||
chr14:100351499
|
CAA | C | 115 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(112): Show | 126 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.725+2186_725+2187d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351499 | ||||||
chr14:100351528
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0001g0116 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.725+2159G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351528 | ||||||
chr14:100351719
|
C | A | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.725+1968G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351719 | ||||||
chr14:100351752
|
G | C | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.725+1935C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351752 | ||||||
chr14:100351760
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.725+1927C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351760 | ||||||
chr14:100351837
|
C | G | 1 | a0001c0002t0002g0030 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.725+1850G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351837 | ||||||
chr14:100351850
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.725+1837C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351850 | ||||||
chr14:100351949
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.725+1738A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351949 | ||||||
chr14:100351987
|
C | T | 1 | a0001c0002t0002g0043 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725+1700G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351987 | ||||||
chr14:100351992
|
C | T | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.725+1695G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100351992 | ||||||
chr14:100352002
|
A | AG | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.725+1684_725+1685i others(3): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352002 | ||||||
chr14:100352002
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0218 | 2 | NA18991.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.725+1685T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352002 | ||||||
chr14:100352108
|
C | CT | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.725+1578dupA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352108 | ||||||
chr14:100352108
|
C | CTT | 22 | a0001c0001t0001g0128a0001c0001t0001g0132a0001c0001t0001g0139others(19): Show | 22 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.725+1577_725+1578d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352108 | ||||||
chr14:100352108
|
CT | C | 9 | a0001c0002t0001g0012a0001c0002t0001g0058a0001c0002t0001g0063others(6): Show | 10 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.725+1578delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352108 | ||||||
chr14:100352108
|
CTTTTT | C | 10 | a0001c0002t0001g0018a0001c0002t0001g0115a0001c0002t0001g0116others(7): Show | 11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.725+1574_725+1578d others(7): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352108 | ||||||
chr14:100352180
|
C | T | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.725+1507G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352180 | ||||||
chr14:100352260
|
C | T | 7 | a0001c0001t0001g0108a0001c0002t0001g0007a0001c0002t0001g0107others(4): Show | 9 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.725+1427G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352260 | ||||||
chr14:100352422
|
C | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.725+1265G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352422 | ||||||
chr14:100352523
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.725+1164A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352523 | ||||||
chr14:100352533
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.725+1154G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352533 | ||||||
chr14:100352587
|
T | G | 1 | a0001c0002t0002g0036 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.725+1100A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352587 | ||||||
chr14:100352652
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.725+1035G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352652 | ||||||
chr14:100352880
|
G | A | 2 | a0001c0002t0001g0115a0001c0002t0001g0116 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.725+807C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352880 | ||||||
chr14:100352948
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.725+739C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352948 | ||||||
chr14:100352953
|
C | T | 2 | a0001c0002t0001g0119a0001c0002t0001g0120 | 2 | HG00639.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.725+734G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100352953 | ||||||
chr14:100353271
|
G | T | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.725+416C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353271 | ||||||
chr14:100353343
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.725+344G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353343 | ||||||
chr14:100353398
|
G | A | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.725+289C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353398 | ||||||
chr14:100353439
|
T | TG | 282 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.725+247dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353439 | ||||||
chr14:100353491
|
G | A | 3 | a0001c0002t0001g0012a0001c0002t0001g0058a0001c0002t0001g0063 | 4 | HG01891.hp2 HG02280.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.725+196C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353491 | ||||||
chr14:100353581
|
T | C | 3 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0064 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.725+106A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 6/10 | chr14 | 100353581 | ||||||
chr14:100353957
|
C | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.543-88G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 5/10 | chr14 | 100353957 | ||||||
chr14:100353996
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.543-127A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 5/10 | chr14 | 100353996 | ||||||
chr14:100354087
|
C | T | 8 | a0001c0001t0001g0108a0001c0002t0001g0007a0001c0002t0001g0107others(5): Show | 10 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.543-218G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 5/10 | chr14 | 100354087 | ||||||
chr14:100354199
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.542+248T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 5/10 | chr14 | 100354199 | ||||||
chr14:100354643
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.423-77C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354643 | ||||||
chr14:100354670
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.423-104A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354670 | ||||||
chr14:100354831
|
TC | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0208a0001c0001t0001g0263others(2): Show | 6 | HG01099.hp2 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.423-266delG | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354831 | ||||||
chr14:100354869
|
G | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.423-303C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354869 | ||||||
chr14:100354898
|
G | A | 1 | a0001c0002t0002g0011 | 2 | NA18940.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.423-332C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354898 | ||||||
chr14:100354935
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.423-369G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100354935 | ||||||
chr14:100355050
|
G | T | 1 | a0001c0001t0001g0249 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.423-484C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355050 | ||||||
chr14:100355185
|
A | C | 1 | a0001c0002t0001g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.423-619T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355185 | ||||||
chr14:100355324
|
G | A | 6 | a0001c0002t0002g0009a0001c0002t0002g0029a0001c0002t0002g0031others(3): Show | 7 | HG02040.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.423-758C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355324 | ||||||
chr14:100355369
|
C | T | 1 | a0001c0002t0002g0038 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.423-803G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355369 | ||||||
chr14:100355444
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02486.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.423-878T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355444 | ||||||
chr14:100355609
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.423-1043A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355609 | ||||||
chr14:100355657
|
A | G | 73 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(70): Show | 76 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.423-1091T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355657 | ||||||
chr14:100355658
|
G | T | 73 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(70): Show | 76 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.423-1092C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355658 | ||||||
chr14:100355812
|
C | T | 10 | a0001c0002t0001g0018a0001c0002t0001g0115a0001c0002t0001g0116others(7): Show | 11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.423-1246G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355812 | ||||||
chr14:100355936
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.423-1370G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355936 | ||||||
chr14:100355964
|
G | A | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.423-1398C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100355964 | ||||||
chr14:100356055
|
T | C | 7 | a0001c0001t0001g0108a0001c0002t0001g0007a0001c0002t0001g0107others(4): Show | 9 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.423-1489A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356055 | ||||||
chr14:100356165
|
T | C | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.423-1599A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356165 | ||||||
chr14:100356227
|
A | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0093others(4): Show | 9 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.423-1661T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356227 | ||||||
chr14:100356382
|
GGT | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 100 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.423-1818_423-1817d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356382 | ||||||
chr14:100356386
|
T | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG02109.hp2 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.423-1820A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356386 | ||||||
chr14:100356394
|
T | TG | 8 | a0001c0001t0001g0174a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.423-1829dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356394 | ||||||
chr14:100356394
|
T | TGG | 4 | a0001c0001t0001g0170a0002c0003t0001g0124a0002c0003t0001g0126others(1): Show | 4 | NA18962.hp1 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-1829_423-1828i others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356394 | ||||||
chr14:100356396
|
T | G | 17 | a0001c0001t0001g0163a0001c0001t0001g0170a0001c0001t0001g0174others(14): Show | 18 | HG00639.hp1 HG01081.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.423-1830A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356396 | ||||||
chr14:100356396
|
T | TG | 48 | a0001c0001t0001g0019a0001c0001t0001g0140a0001c0001t0001g0141others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.423-1831dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356396 | ||||||
chr14:100356396
|
T | TGG | 12 | a0001c0001t0001g0143a0001c0001t0001g0157a0001c0001t0001g0159others(9): Show | 12 | HG01074.hp1 HG02132.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.423-1831_423-1830i others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356396 | ||||||
chr14:100356396
|
T | TGGG | 7 | a0001c0001t0001g0139a0001c0001t0001g0169a0001c0001t0001g0194others(4): Show | 8 | HG00621.hp1 HG01891.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.423-1831_423-1830i others(5): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356396 | ||||||
chr14:100356397
|
GT | G | 39 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0150others(36): Show | 43 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.423-1832delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356397 | ||||||
chr14:100356398
|
T | G | 90 | a0001c0001t0001g0019a0001c0001t0001g0139a0001c0001t0001g0140others(87): Show | 93 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.423-1832A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356398 | ||||||
chr14:100356398
|
T | TG | 27 | a0001c0001t0001g0008a0001c0001t0001g0152a0001c0001t0001g0164others(24): Show | 35 | HG00738.hp2 HG01175.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.423-1833dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356398 | ||||||
chr14:100356398
|
TGG | T | 29 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0216others(26): Show | 30 | HG00438.hp1 HG01891.hp2 HG02280.hp1 others(27): Show |
intron_variant | MODIFIER | c.423-1834_423-1833d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356398 | ||||||
chr14:100356400
|
G | T | 1 | a0001c0002t0001g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.423-1834C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356400 | ||||||
chr14:100356555
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.423-1989A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356555 | ||||||
chr14:100356679
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.423-2113T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356679 | ||||||
chr14:100356725
|
T | G | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.423-2159A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356725 | ||||||
chr14:100356971
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.423-2405C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356971 | ||||||
chr14:100356987
|
C | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG02109.hp2 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.423-2421G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100356987 | ||||||
chr14:100357005
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.423-2439G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357005 | ||||||
chr14:100357158
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0282 | 2 | HG00673.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.423-2592A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357158 | ||||||
chr14:100357378
|
C | A | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.423-2812G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357378 | ||||||
chr14:100357571
|
C | T | 39 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(36): Show | 47 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.422+2983G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357571 | ||||||
chr14:100357607
|
G | A | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.422+2947C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357607 | ||||||
chr14:100357712
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.422+2842G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357712 | ||||||
chr14:100357749
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.422+2805G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357749 | ||||||
chr14:100357832
|
T | C | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+2722A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357832 | ||||||
chr14:100357938
|
T | C | 1 | a0001c0002t0001g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.422+2616A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100357938 | ||||||
chr14:100358018
|
C | T | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.422+2536G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358018 | ||||||
chr14:100358052
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.422+2502C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358052 | ||||||
chr14:100358079
|
C | G | 1 | a0001c0001t0001g0190 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.422+2475G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358079 | ||||||
chr14:100358157
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.422+2397G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358157 | ||||||
chr14:100358170
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.422+2384G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358170 | ||||||
chr14:100358202
|
G | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.422+2352C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358202 | ||||||
chr14:100358219
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.422+2335C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358219 | ||||||
chr14:100358220
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0176 | 2 | NA18946.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.422+2334G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358220 | ||||||
chr14:100358226
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.422+2328C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358226 | ||||||
chr14:100358303
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.422+2251A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358303 | ||||||
chr14:100358359
|
C | CCT | 10 | a0001c0002t0001g0018a0001c0002t0001g0115a0001c0002t0001g0116others(7): Show | 11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.422+2193_422+2194d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358359 | ||||||
chr14:100358678
|
G | T | 1 | a0001c0002t0001g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.422+1876C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100358678 | ||||||
chr14:100359118
|
A | G | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.422+1436T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359118 | ||||||
chr14:100359119
|
A | T | 1 | a0001c0002t0001g0075 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.422+1435T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359119 | ||||||
chr14:100359239
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.422+1315C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359239 | ||||||
chr14:100359286
|
G | C | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.422+1268C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359286 | ||||||
chr14:100359333
|
C | T | 73 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(70): Show | 76 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.422+1221G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359333 | ||||||
chr14:100359439
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.422+1115G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359439 | ||||||
chr14:100359544
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.422+1010A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359544 | ||||||
chr14:100359551
|
C | T | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.422+1003G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359551 | ||||||
chr14:100359863
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 123 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.422+691C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359863 | ||||||
chr14:100359923
|
G | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.422+631C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100359923 | ||||||
chr14:100360074
|
C | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0174a0001c0001t0001g0184 | 3 | HG01081.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.422+480G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360074 | ||||||
chr14:100360098
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.422+456T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360098 | ||||||
chr14:100360321
|
C | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0093others(4): Show | 9 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.422+233G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360321 | ||||||
chr14:100360394
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.422+160G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360394 | ||||||
chr14:100360404
|
C | T | 1 | a0002c0003t0001g0124 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.422+150G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360404 | ||||||
chr14:100360436
|
C | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.422+118G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360436 | ||||||
chr14:100360470
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.422+84A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360470 | ||||||
chr14:100360471
|
G | T | 1 | a0001c0001t0001g0146 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.422+83C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 4/10 | chr14 | 100360471 | ||||||
chr14:100360728
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.314-66A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100360728 | ||||||
chr14:100360805
|
C | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.314-143G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100360805 | ||||||
chr14:100360805
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.314-143G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100360805 | ||||||
chr14:100360997
|
G | GTA | 6 | a0001c0002t0002g0009a0001c0002t0002g0029a0001c0002t0002g0031others(3): Show | 7 | HG02040.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-337_314-336dup others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100360997 | ||||||
chr14:100360997
|
GTA | G | 7 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0093others(4): Show | 9 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.314-337_314-336del others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100360997 | ||||||
chr14:100361092
|
G | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.314-430C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100361092 | ||||||
chr14:100361171
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.314-509G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100361171 | ||||||
chr14:100361234
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.313+474T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100361234 | ||||||
chr14:100361305
|
A | G | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.313+403T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100361305 | ||||||
chr14:100361341
|
T | C | 1 | a0001c0002t0002g0046 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.313+367A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 3/10 | chr14 | 100361341 | ||||||
chr14:100362060
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.100-139A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362060 | ||||||
chr14:100362126
|
T | C | 1 | a0001c0002t0002g0044 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.100-205A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362126 | ||||||
chr14:100362150
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.100-229G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362150 | ||||||
chr14:100362288
|
C | T | 30 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(27): Show | 34 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.100-367G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362288 | ||||||
chr14:100362346
|
T | C | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-425A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362346 | ||||||
chr14:100362533
|
G | GA | 37 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(34): Show | 45 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.100-613dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362533 | ||||||
chr14:100362847
|
C | T | 44 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(41): Show | 50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-926G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100362847 | ||||||
chr14:100363227
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | NA19064.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.100-1306T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363227 | ||||||
chr14:100363266
|
A | T | 44 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(41): Show | 50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-1345T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363266 | ||||||
chr14:100363268
|
TTAACCAA others(5): Show |
T | 44 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(41): Show | 50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-1359_100-1348d others(14): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363268 | ||||||
chr14:100363511
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 125 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.100-1590G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363511 | ||||||
chr14:100363521
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.100-1600G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363521 | ||||||
chr14:100363654
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.100-1733T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363654 | ||||||
chr14:100363839
|
C | A | 1 | a0001c0001t0001g0296 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100-1918G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363839 | ||||||
chr14:100363922
|
C | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.100-2001G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100363922 | ||||||
chr14:100364036
|
T | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG02109.hp2 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.100-2115A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364036 | ||||||
chr14:100364055
|
C | G | 5 | a0001c0002t0001g0068a0001c0002t0001g0074a0001c0002t0001g0087others(2): Show | 5 | HG00558.hp1 HG02165.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-2134G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364055 | ||||||
chr14:100364214
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.100-2293T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364214 | ||||||
chr14:100364254
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100-2333C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364254 | ||||||
chr14:100364288
|
C | G | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-2367G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364288 | ||||||
chr14:100364289
|
A | C | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-2368T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364289 | ||||||
chr14:100364290
|
G | A | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-2369C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364290 | ||||||
chr14:100364418
|
A | T | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-2497T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364418 | ||||||
chr14:100364481
|
C | A | 44 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(41): Show | 50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-2560G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364481 | ||||||
chr14:100364483
|
C | G | 2 | a0001c0002t0001g0115a0001c0002t0001g0116 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.100-2562G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364483 | ||||||
chr14:100364581
|
T | G | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-2660A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364581 | ||||||
chr14:100364820
|
G | C | 2 | a0001c0002t0001g0115a0001c0002t0001g0116 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.100-2899C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364820 | ||||||
chr14:100364906
|
A | G | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-2985T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364906 | ||||||
chr14:100364910
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.100-2989T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364910 | ||||||
chr14:100364973
|
A | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.100-3052T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100364973 | ||||||
chr14:100365037
|
T | G | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-3116A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365037 | ||||||
chr14:100365038
|
G | T | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-3117C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365038 | ||||||
chr14:100365124
|
T | TAC | 76 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0019others(73): Show | 83 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.100-3205_100-3204d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | ||||||
chr14:100365124
|
T | TACAC | 56 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0108others(53): Show | 62 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.100-3207_100-3204d others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | ||||||
chr14:100365124
|
T | TACACAC | 32 | a0001c0001t0001g0186a0001c0001t0001g0195a0001c0001t0001g0271others(29): Show | 39 | HG01175.hp1 HG01433.hp2 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.100-3209_100-3204d others(8): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | ||||||
chr14:100365124
|
T | TACACACA others(1): Show |
17 | a0001c0001t0003g0262a0001c0002t0001g0012a0001c0002t0001g0013others(14): Show | 20 | HG01169.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-3211_100-3204d others(10): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | ||||||
chr14:100365124
|
T | TACACACA others(3): Show |
15 | a0001c0002t0001g0005a0001c0002t0001g0053a0001c0002t0001g0054others(12): Show | 17 | HG00140.hp2 HG00544.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-3213_100-3204d others(12): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | ||||||
chr14:100365124
|
T | TACACACA others(5): Show |
4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0001g0123others(1): Show | 4 | HG00423.hp1 HG02622.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-3215_100-3204d others(14): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | ||||||
chr14:100365124
|
T | TACACACA others(7): Show |
4 | a0001c0002t0001g0068a0001c0002t0001g0083a0001c0002t0001g0087others(1): Show | 4 | HG00558.hp1 NA18999.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3217_100-3204d others(16): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | ||||||
chr14:100365124
|
TACAC | T | 4 | a0001c0001t0001g0131a0001c0001t0001g0214a0001c0001t0001g0251others(1): Show | 6 | HG01515.hp1 HG02109.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-3207_100-3204d others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | ||||||
chr14:100365124
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0151 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.100-3213_100-3204d others(12): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365124 | ||||||
chr14:100365155
|
A | ACACACAC others(4): Show |
1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100-3235_100-3234i others(13): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365155 | ||||||
chr14:100365162
|
C | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0246a0001c0001t0001g0283 | 3 | HG02129.hp2 NA18970.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.100-3241G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365162 | ||||||
chr14:100365163
|
A | ACACACAC others(4): Show |
2 | a0001c0002t0001g0051a0001c0002t0001g0069 | 2 | HG02056.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.100-3243_100-3242i others(13): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365163 | ||||||
chr14:100365220
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.100-3299C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365220 | ||||||
chr14:100365270
|
TAACAGGA others(13): Show |
T | 73 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0139others(70): Show | 76 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.100-3369_100-3350d others(22): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365270 | ||||||
chr14:100365437
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.100-3516C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365437 | ||||||
chr14:100365452
|
C | T | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-3531G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365452 | ||||||
chr14:100365498
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.100-3577G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365498 | ||||||
chr14:100365559
|
G | A | 8 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(5): Show | 8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+3528C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365559 | ||||||
chr14:100365579
|
C | CA | 12 | a0001c0001t0001g0143a0001c0001t0001g0164a0001c0001t0001g0165others(9): Show | 13 | HG01891.hp1 HG02145.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+3507dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365579 | ||||||
chr14:100365579
|
CA | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.99+3507delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365579 | ||||||
chr14:100365579
|
CAA | C | 37 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(34): Show | 45 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.99+3506_99+3507del others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365579 | ||||||
chr14:100365728
|
CT | C | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(189): Show | 208 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.99+3358delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365728 | ||||||
chr14:100365728
|
CTT | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0187others(43): Show | 59 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.99+3357_99+3358del others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365728 | ||||||
chr14:100365732
|
T | C | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+3355A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365732 | ||||||
chr14:100365870
|
T | A | 8 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(5): Show | 8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+3217A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365870 | ||||||
chr14:100365873
|
T | C | 10 | a0001c0002t0001g0018a0001c0002t0001g0115a0001c0002t0001g0116others(7): Show | 11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+3214A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365873 | ||||||
chr14:100365915
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(74): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.99+3172G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365915 | ||||||
chr14:100365945
|
C | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.99+3142G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100365945 | ||||||
chr14:100366040
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.99+3047G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366040 | ||||||
chr14:100366054
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.99+3033A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366054 | ||||||
chr14:100366081
|
T | G | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+3006A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366081 | ||||||
chr14:100366112
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99+2975C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366112 | ||||||
chr14:100366252
|
C | G | 1 | a0001c0002t0002g0047 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.99+2835G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366252 | ||||||
chr14:100366322
|
C | T | 1 | a0001c0002t0002g0031 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.99+2765G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366322 | ||||||
chr14:100366463
|
A | G | 7 | a0001c0001t0001g0108a0001c0002t0001g0007a0001c0002t0001g0107others(4): Show | 9 | HG02280.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+2624T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366463 | ||||||
chr14:100366464
|
C | T | 1 | a0001c0002t0001g0068 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.99+2623G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366464 | ||||||
chr14:100366572
|
A | C | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+2515T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366572 | ||||||
chr14:100366762
|
G | T | 2 | a0001c0002t0001g0115a0001c0002t0001g0116 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.99+2325C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366762 | ||||||
chr14:100366799
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+2288T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366799 | ||||||
chr14:100366805
|
T | A | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+2282A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100366805 | ||||||
chr14:100367048
|
TA | T | 14 | a0001c0002t0001g0018a0001c0002t0001g0115a0001c0002t0001g0116others(11): Show | 15 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+2038delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367048 | ||||||
chr14:100367282
|
G | T | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+1805C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367282 | ||||||
chr14:100367328
|
G | A | 2 | a0001c0002t0001g0005a0001c0002t0001g0091 | 4 | NA18973.hp1 NA18974.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1759C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367328 | ||||||
chr14:100367405
|
T | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1682A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367405 | ||||||
chr14:100367416
|
C | T | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.99+1671G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367416 | ||||||
chr14:100367456
|
C | T | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.99+1631G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367456 | ||||||
chr14:100367570
|
A | C | 1 | a0001c0001t0001g0140 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.99+1517T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367570 | ||||||
chr14:100367579
|
T | G | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+1508A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367579 | ||||||
chr14:100367587
|
C | CG | 9 | a0001c0001t0001g0188a0001c0001t0001g0200a0001c0001t0001g0208others(6): Show | 9 | HG01099.hp2 HG01175.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+1499dupC | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367587 | ||||||
chr14:100367594
|
C | G | 1 | a0001c0001t0001g0273 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.99+1493G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367594 | ||||||
chr14:100367608
|
C | CA | 18 | a0001c0001t0001g0136a0001c0001t0001g0143a0001c0001t0001g0144others(15): Show | 18 | HG00438.hp2 HG00621.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+1478dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367608 | ||||||
chr14:100367608
|
CA | C | 79 | a0001c0001t0001g0130a0001c0001t0001g0159a0001c0001t0001g0160others(76): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.99+1478delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367608 | ||||||
chr14:100367608
|
CAA | C | 19 | a0001c0002t0001g0012a0001c0002t0001g0017a0001c0002t0001g0055others(16): Show | 21 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+1477_99+1478del others(2): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367608 | ||||||
chr14:100367674
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0208a0001c0001t0001g0263others(2): Show | 6 | HG01099.hp2 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+1413C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367674 | ||||||
chr14:100367678
|
A | C | 2 | a0001c0002t0001g0066a0001c0002t0001g0067 | 2 | HG00323.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.99+1409T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367678 | ||||||
chr14:100367966
|
TA | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.99+1120delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367966 | ||||||
chr14:100367977
|
G | A | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+1110C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100367977 | ||||||
chr14:100368000
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99+1087G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368000 | ||||||
chr14:100368156
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.99+931A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368156 | ||||||
chr14:100368205
|
T | C | 43 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0097others(40): Show | 51 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.99+882A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368205 | ||||||
chr14:100368229
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.99+858G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368229 | ||||||
chr14:100368451
|
CCTGAAAG others(9): Show |
C | 1 | a0001c0002t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.99+620_99+635delAG others(14): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368451 | ||||||
chr14:100368538
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.99+549C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368538 | ||||||
chr14:100368645
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.99+442A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368645 | ||||||
chr14:100368706
|
A | G | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.99+381T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368706 | ||||||
chr14:100368785
|
ACCC | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.99+299_99+301delGG others(1): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 2/10 | chr14 | 100368785 | ||||||
chr14:100369466
|
T | C | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-73-208A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369466 | ||||||
chr14:100369483
|
T | C | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-225A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369483 | ||||||
chr14:100369539
|
C | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0266 | 3 | HG02572.hp1 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-73-281G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369539 | ||||||
chr14:100369598
|
T | C | 50 | a0001c0002t0001g0012a0001c0002t0001g0018a0001c0002t0001g0033others(47): Show | 59 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-73-340A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369598 | ||||||
chr14:100369641
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.-73-383A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369641 | ||||||
chr14:100369681
|
AT | A | 19 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(16): Show | 20 | HG01891.hp2 HG02258.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-73-424delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369681 | ||||||
chr14:100369781
|
G | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-73-523C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369781 | ||||||
chr14:100369827
|
C | T | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73-569G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369827 | ||||||
chr14:100369828
|
G | A | 8 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(5): Show | 8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73-570C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369828 | ||||||
chr14:100369908
|
CTCACTTC others(13): Show |
C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-73-670_-73-651del others(20): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369908 | ||||||
chr14:100369918
|
C | T | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-73-660G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100369918 | ||||||
chr14:100370016
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-73-758G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370016 | ||||||
chr14:100370066
|
T | C | 1 | a0001c0002t0001g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-73-808A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370066 | ||||||
chr14:100370072
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.-73-814G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370072 | ||||||
chr14:100370285
|
A | G | 1 | a0001c0002t0002g0028 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-73-1027T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370285 | ||||||
chr14:100370344
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-73-1086T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370344 | ||||||
chr14:100370436
|
C | T | 10 | a0001c0002t0001g0018a0001c0002t0001g0115a0001c0002t0001g0116others(7): Show | 11 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-73-1178G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370436 | ||||||
chr14:100370439
|
C | T | 38 | a0001c0002t0001g0018a0001c0002t0001g0033a0001c0002t0001g0115others(35): Show | 46 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-73-1181G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370439 | ||||||
chr14:100370637
|
A | C | 1 | a0001c0001t0001g0209 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-73-1379T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370637 | ||||||
chr14:100370646
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-73-1388T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370646 | ||||||
chr14:100370657
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-73-1399A>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370657 | ||||||
chr14:100370782
|
G | GA | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.-73-1525dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370782 | ||||||
chr14:100370782
|
G | GAA | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0137others(6): Show | 9 | HG02257.hp1 HG02818.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73-1526_-73-1525d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370782 | ||||||
chr14:100370826
|
C | T | 1 | a0001c0002t0001g0107 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-73-1568G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370826 | ||||||
chr14:100370875
|
C | A | 1 | a0001c0002t0002g0046 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-73-1617G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370875 | ||||||
chr14:100370893
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.-73-1635G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370893 | ||||||
chr14:100370927
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0208 | 3 | HG01099.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-73-1669T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100370927 | ||||||
chr14:100371045
|
C | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-73-1787G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371045 | ||||||
chr14:100371445
|
C | T | 8 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0118others(5): Show | 9 | HG00639.hp1 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-2187G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371445 | ||||||
chr14:100371447
|
C | CA | 8 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(5): Show | 8 | HG01175.hp1 HG01361.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73-2190dupT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-73-2201_-73-2190d others(14): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG01074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-73-2202_-73-2190d others(15): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01081.hp1 HG01081.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-73-2203_-73-2190d others(16): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0164 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-73-2208_-73-2190d others(21): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0139 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-73-2209_-73-2190d others(22): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0165a0001c0001t0001g0273 | 2 | HG03834.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(25): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(17): Show |
11 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0145others(8): Show | 11 | HG01975.hp2 HG02015.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(26): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(18): Show |
20 | a0001c0001t0001g0008a0001c0001t0001g0142a0001c0001t0001g0143others(17): Show | 22 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(27): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(19): Show |
7 | a0001c0001t0001g0019a0001c0001t0001g0190a0001c0001t0001g0191others(4): Show | 8 | HG00733.hp1 HG01433.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(28): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(20): Show |
5 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | HG01175.hp2 HG01934.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(29): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(21): Show |
3 | a0001c0001t0001g0196a0001c0001t0001g0206a0001c0001t0001g0277 | 3 | HG01361.hp1 HG04115.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(30): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(22): Show |
2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG00738.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(31): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(23): Show |
4 | a0001c0001t0001g0144a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG00438.hp2 HG01243.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(32): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-73-2190_-73-2189i others(33): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | NA18974.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-73-2190_-73-2189i others(34): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-73-2190_-73-2189i others(26): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
CA | C | 13 | a0001c0001t0001g0151a0001c0002t0001g0012a0001c0002t0001g0052others(10): Show | 14 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-73-2190delT | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371447
|
CAAAAAAA others(3): Show |
C | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 125 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-73-2199_-73-2190d others(12): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371447 | ||||||
chr14:100371537
|
C | A | 6 | a0001c0002t0001g0017a0001c0002t0001g0100a0001c0002t0001g0101others(3): Show | 7 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73-2279G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371537 | ||||||
chr14:100371569
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-73-2311G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371569 | ||||||
chr14:100371608
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-73-2350T>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371608 | ||||||
chr14:100371670
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-73-2412C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371670 | ||||||
chr14:100371825
|
C | T | 1 | a0001c0002t0002g0027 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-73-2567G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371825 | ||||||
chr14:100371836
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-73-2578C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371836 | ||||||
chr14:100371911
|
G | T | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-73-2653C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371911 | ||||||
chr14:100371915
|
C | G | 1 | a0001c0002t0001g0065 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-73-2657G>C | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371915 | ||||||
chr14:100371982
|
GCCTTAAC others(6): Show |
G | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-73-2737_-73-2725d others(15): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100371982 | ||||||
chr14:100372068
|
C | A | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-73-2810G>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372068 | ||||||
chr14:100372318
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-74+2965A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372318 | ||||||
chr14:100372442
|
G | C | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-74+2841C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372442 | ||||||
chr14:100372791
|
G | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-74+2492C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372791 | ||||||
chr14:100372822
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-74+2461C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372822 | ||||||
chr14:100372837
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-74+2446A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372837 | ||||||
chr14:100372924
|
G | T | 37 | a0001c0002t0001g0005a0001c0002t0001g0013a0001c0002t0001g0014others(34): Show | 41 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.-74+2359C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100372924 | ||||||
chr14:100373150
|
CT | C | 4 | a0002c0003t0001g0124a0002c0003t0001g0125a0002c0003t0001g0126others(1): Show | 4 | NA18973.hp2 NA18985.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-74+2132delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373150 | ||||||
chr14:100373201
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-74+2082T>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373201 | ||||||
chr14:100373410
|
G | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-74+1873C>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373410 | ||||||
chr14:100373581
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-74+1702C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373581 | ||||||
chr14:100373681
|
T | C | 12 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(9): Show | 13 | HG01891.hp2 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-74+1602A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373681 | ||||||
chr14:100373712
|
T | C | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-74+1571A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373712 | ||||||
chr14:100373761
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-74+1522A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373761 | ||||||
chr14:100373824
|
TTG | T | 15 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(12): Show | 17 | HG00423.hp1 HG02027.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-74+1457_-74+1458d others(4): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | ||||||
chr14:100373824
|
TTGTG | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-74+1455_-74+1458d others(6): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | ||||||
chr14:100373824
|
TTGTGTG | T | 74 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0144others(71): Show | 78 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.-74+1453_-74+1458d others(8): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | ||||||
chr14:100373824
|
TTGTGTGT others(1): Show |
T | 56 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(53): Show | 62 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-74+1451_-74+1458d others(10): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | ||||||
chr14:100373824
|
TTGTGTGT others(3): Show |
T | 21 | a0001c0002t0001g0012a0001c0002t0001g0018a0001c0002t0001g0052others(18): Show | 23 | HG00639.hp1 HG01891.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.-74+1449_-74+1458d others(12): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | ||||||
chr14:100373824
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0002t0001g0051 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-74+1447_-74+1458d others(14): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | ||||||
chr14:100373824
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0002t0001g0117 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-74+1445_-74+1458d others(16): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | ||||||
chr14:100373824
|
TTGTGTGT others(9): Show |
T | 2 | a0001c0002t0001g0115a0001c0002t0001g0116 | 2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-74+1443_-74+1458d others(18): Show |
WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373824 | ||||||
chr14:100373953
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-74+1330G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100373953 | ||||||
chr14:100374066
|
T | A | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.-74+1217A>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374066 | ||||||
chr14:100374146
|
G | A | 2 | a0001c0005t0001g0290a0001c0005t0001g0291 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-74+1137C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374146 | ||||||
chr14:100374215
|
T | C | 8 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(5): Show | 8 | HG02486.hp2 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-74+1068A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374215 | ||||||
chr14:100374259
|
G | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-74+1024C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374259 | ||||||
chr14:100374476
|
T | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-74+807A>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374476 | ||||||
chr14:100374613
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-74+670C>T | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374613 | ||||||
chr14:100374671
|
G | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-74+612C>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374671 | ||||||
chr14:100374757
|
A | C | 28 | a0001c0002t0001g0033a0001c0002t0002g0002a0001c0002t0002g0009others(25): Show | 35 | HG00099.hp1 HG00423.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.-74+526T>G | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374757 | ||||||
chr14:100374829
|
AT | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-74+453delA | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100374829 | ||||||
chr14:100375235
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-74+48G>A | WARS1 | ENSG00000140105.18 | transcript | ENST00000392882.7 | protein_coding | 1/10 | chr14 | 100375235 |