geneid | 2617 |
---|---|
ensemblid | ENSG00000106105.15 |
hgncid | 4162 |
symbol | GARS1 |
name | glycyl-tRNA synthetase 1 |
refseq_nuc | NM_002047.4 |
refseq_prot | NP_002038.2 |
ensembl_nuc | ENST00000389266.8 |
ensembl_prot | ENSP00000373918.3 |
mane_status | MANE Select |
chr | chr7 |
start | 30594878 |
end | 30634033 |
strand | + |
ver | v1.2 |
region | chr7:30594878-30634033 |
region5000 | chr7:30589878-30639033 |
regionname0 | GARS1_chr7_30594878_30634033 |
regionname5000 | GARS1_chr7_30589878_30639033 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 739 | 233 | 42 | 41 | 110 | 10 | 29 | 83 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0002 | 1/0 | 739 | 158 | 43 | 26 | 69 | 6 | 13 | 55 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0003 | 0/0 | 739 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0004 | 0/0 | 739 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0005 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0006 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0007 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0008 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0009 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2220 | 156 | 43 | 25 | 68 | 6 | 13 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0002 | 0/1 | 2220 | 123 | 8 | 25 | 64 | 10 | 15 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0003 | 0/0 | 2220 | 79 | 9 | 10 | 46 | 0 | 14 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0004 | 0/0 | 2220 | 17 | 15 | 2 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0005 | 0/0 | 2220 | 7 | 6 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0006 | 0/0 | 2220 | 5 | 5 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0007 | 0/0 | 2220 | 5 | 3 | 2 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0008 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0009 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0010 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0011 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0012 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0013 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0014 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0015 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0016 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
c0017 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
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 | 1/0 | 218 | 172 | 54 | 29 | 69 | 6 | 13 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
t0002 | 0/1 | 217 | 149 | 28 | 28 | 67 | 10 | 15 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
t0003 | 0/0 | 216 | 80 | 10 | 10 | 46 | 0 | 14 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
t0004 | 0/0 | 217 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
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 | 0/1 | 32 | 1 | 7 | 19 | 2 | 2 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0002 | 1/0 | 15 | 0 | 0 | 14 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0003 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0004 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0005 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0006 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0007 | 0/0 | 8 | 1 | 6 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0008 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0013 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0015 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0021 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0022 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/1 | 2220 | 123 | 8 | 25 | 64 | 10 | 15 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0003 | 0/0 | 2220 | 79 | 9 | 10 | 46 | 0 | 14 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0004 | 0/0 | 2220 | 17 | 15 | 2 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0005 | 0/0 | 2220 | 7 | 6 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0007 | 0/0 | 2220 | 5 | 3 | 2 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0013 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0015 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0002c0001 | 1/0 | 2220 | 156 | 43 | 25 | 68 | 6 | 13 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0002c0008 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0002c0011 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0003c0006 | 0/0 | 2220 | 5 | 5 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0004c0010 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0005c0014 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0006c0009 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0007c0016 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0008c0012 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0009c0017 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 2437 | 3 | 3 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0002t0002 | 0/1 | 2436 | 119 | 5 | 24 | 64 | 10 | 15 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0002t0004 | 0/0 | 2436 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0003t0002 | 0/0 | 2436 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0003t0003 | 0/0 | 2435 | 78 | 9 | 9 | 46 | 0 | 14 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0004t0002 | 0/0 | 2436 | 17 | 15 | 2 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0005t0002 | 0/0 | 2436 | 7 | 6 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0007t0001 | 0/0 | 2437 | 5 | 3 | 2 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0013t0002 | 0/0 | 2436 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0001c0015t0001 | 0/0 | 2437 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0002c0001t0001 | 1/0 | 2437 | 156 | 43 | 25 | 68 | 6 | 13 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0002c0008t0001 | 0/0 | 2437 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0002c0011t0001 | 0/0 | 2437 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0003c0006t0001 | 0/0 | 2437 | 5 | 5 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0004c0010t0003 | 0/0 | 2435 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0005c0014t0002 | 0/0 | 2436 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0006c0009t0003 | 0/0 | 2435 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0007c0016t0002 | 0/0 | 2436 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0008c0012t0002 | 0/0 | 2436 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
a0009c0017t0002 | 0/0 | 2436 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | copy fasta | chr7 | 30589878 | 30639033 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0001 | 0/1 | 31 | 1 | 7 | 18 | 2 | 2 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0021 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0002t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0006 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0013 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0003t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0004t0002g0005 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0004t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0004t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0004t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0004t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0004t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0004t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0004t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0005t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0005t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0005t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0005t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0005t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0007t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0007t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0007t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0007t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0013t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0001c0015t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0002 | 1/0 | 15 | 0 | 0 | 14 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0003 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0004 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0007 | 0/0 | 8 | 1 | 6 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0008 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0008t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0002c0011t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0003c0006t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0003c0006t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0003c0006t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0003c0006t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0004c0010t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0005c0014t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0006c0009t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0007c0016t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0008c0012t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
a0009c0017t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0085 | EUR | GBR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00099 | hp2 | a0002 | c0001 | t0001 | g0100 | EUR | GBR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0148 | EUR | GBR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0021 | EUR | FIN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00280 | hp2 | a0002 | c0001 | t0001 | g0032 | EUR | FIN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0177 | EUR | FIN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0138 | EUR | FIN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00408 | hp1 | a0002 | c0001 | t0001 | g0107 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00408 | hp2 | a0002 | c0001 | t0001 | g0029 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00438 | hp2 | a0002 | c0001 | t0001 | g0120 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00544 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00558 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00558 | hp2 | a0001 | c0003 | t0003 | g0040 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00597 | hp2 | a0008 | c0012 | t0002 | g0009 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00609 | hp1 | a0001 | c0003 | t0003 | g0039 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00621 | hp2 | a0002 | c0001 | t0001 | g0121 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00639 | hp1 | a0001 | c0015 | t0001 | g0011 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00673 | hp1 | a0001 | c0003 | t0003 | g0039 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00738 | hp1 | a0001 | c0003 | t0003 | g0236 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00738 | hp2 | a0002 | c0001 | t0001 | g0032 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00741 | hp1 | a0002 | c0001 | t0001 | g0131 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01069 | hp2 | a0001 | c0007 | t0001 | g0024 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01070 | hp1 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0132 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01071 | hp1 | a0001 | c0007 | t0001 | g0056 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01071 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01074 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01081 | hp1 | a0001 | c0003 | t0003 | g0235 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01081 | hp2 | a0001 | c0004 | t0002 | g0053 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01099 | hp1 | a0001 | c0003 | t0003 | g0207 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0189 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01106 | hp1 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01106 | hp2 | a0002 | c0001 | t0001 | g0064 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01109 | hp1 | a0001 | c0004 | t0002 | g0005 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01109 | hp2 | a0002 | c0001 | t0001 | g0008 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01167 | hp1 | a0002 | c0001 | t0001 | g0061 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01167 | hp2 | a0004 | c0010 | t0003 | g0216 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01168 | hp1 | a0002 | c0001 | t0001 | g0117 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01168 | hp2 | a0002 | c0001 | t0001 | g0015 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01169 | hp1 | a0002 | c0001 | t0001 | g0065 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01169 | hp2 | a0002 | c0001 | t0001 | g0086 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01175 | hp1 | a0001 | c0003 | t0003 | g0237 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01175 | hp2 | a0002 | c0001 | t0001 | g0109 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01192 | hp1 | a0001 | c0003 | t0002 | g0240 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0157 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01243 | hp1 | a0002 | c0001 | t0001 | g0062 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | PUR | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01255 | hp1 | a0001 | c0003 | t0003 | g0210 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0143 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0158 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0137 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01346 | hp1 | a0002 | c0001 | t0001 | g0083 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01358 | hp1 | a0001 | c0003 | t0003 | g0206 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01358 | hp2 | a0001 | c0003 | t0003 | g0221 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01433 | hp1 | a0001 | c0003 | t0003 | g0038 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0192 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01516 | hp1 | a0002 | c0001 | t0001 | g0015 | EUR | IBS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0022 | EUR | IBS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01517 | hp1 | a0002 | c0001 | t0001 | g0015 | EUR | IBS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01884 | hp1 | a0002 | c0001 | t0001 | g0059 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01884 | hp2 | a0001 | c0004 | t0002 | g0005 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01891 | hp1 | a0002 | c0001 | t0001 | g0010 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01891 | hp2 | a0001 | c0005 | t0002 | g0054 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01928 | hp2 | a0002 | c0001 | t0001 | g0095 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01934 | hp1 | a0002 | c0011 | t0001 | g0003 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0164 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01943 | hp2 | a0002 | c0001 | t0001 | g0084 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01978 | hp1 | a0001 | c0005 | t0002 | g0045 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01981 | hp1 | a0001 | c0002 | t0004 | g0042 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01981 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0166 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02004 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02015 | hp1 | a0001 | c0003 | t0003 | g0243 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02027 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02040 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02055 | hp1 | a0001 | c0004 | t0002 | g0005 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02055 | hp2 | a0002 | c0001 | t0001 | g0010 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02071 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02074 | hp1 | a0001 | c0003 | t0003 | g0231 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02074 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02080 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02129 | hp1 | a0001 | c0003 | t0003 | g0228 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02145 | hp1 | a0001 | c0003 | t0003 | g0246 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02145 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02155 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | CDX | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02155 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | CDX | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0108 | EAS | CDX | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | CDX | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02257 | hp1 | a0003 | c0006 | t0001 | g0079 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02257 | hp2 | a0002 | c0001 | t0001 | g0018 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02258 | hp1 | a0002 | c0001 | t0001 | g0027 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02258 | hp2 | a0002 | c0001 | t0001 | g0089 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02273 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02280 | hp1 | a0003 | c0006 | t0001 | g0028 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02280 | hp2 | a0001 | c0004 | t0002 | g0051 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0165 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02293 | hp2 | a0002 | c0001 | t0001 | g0087 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0090 | AMR | PEL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02523 | hp1 | a0001 | c0003 | t0003 | g0232 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | KHV | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02572 | hp1 | a0002 | c0001 | t0001 | g0027 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02572 | hp2 | a0002 | c0001 | t0001 | g0081 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02602 | hp1 | a0001 | c0003 | t0003 | g0229 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0182 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02615 | hp2 | a0002 | c0001 | t0001 | g0010 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02622 | hp2 | a0002 | c0001 | t0001 | g0018 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02630 | hp1 | a0002 | c0001 | t0001 | g0025 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02630 | hp2 | a0001 | c0004 | t0002 | g0200 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02647 | hp1 | a0001 | c0007 | t0001 | g0024 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02647 | hp2 | a0002 | c0001 | t0001 | g0077 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02683 | hp2 | a0001 | c0003 | t0003 | g0006 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02698 | hp1 | a0001 | c0003 | t0003 | g0220 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0020 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02717 | hp1 | a0001 | c0003 | t0003 | g0212 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02717 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02723 | hp1 | a0002 | c0001 | t0001 | g0067 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02735 | hp1 | a0001 | c0003 | t0003 | g0013 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02735 | hp2 | a0002 | c0001 | t0001 | g0102 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02738 | hp1 | a0001 | c0003 | t0003 | g0242 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0150 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02809 | hp2 | a0002 | c0001 | t0001 | g0074 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02818 | hp1 | a0003 | c0006 | t0001 | g0078 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02818 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02886 | hp1 | a0001 | c0003 | t0003 | g0209 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02886 | hp2 | a0002 | c0001 | t0001 | g0072 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02895 | hp1 | a0002 | c0001 | t0001 | g0073 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02895 | hp2 | a0001 | c0007 | t0001 | g0058 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02896 | hp1 | a0002 | c0001 | t0001 | g0025 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02896 | hp2 | a0001 | c0004 | t0002 | g0049 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02897 | hp1 | a0001 | c0004 | t0002 | g0050 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02897 | hp2 | a0002 | c0001 | t0001 | g0071 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0134 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02922 | hp2 | a0001 | c0003 | t0003 | g0211 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02970 | hp1 | a0001 | c0013 | t0002 | g0048 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02970 | hp2 | a0002 | c0001 | t0001 | g0082 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0088 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02976 | hp2 | a0001 | c0003 | t0003 | g0214 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03041 | hp1 | a0001 | c0004 | t0002 | g0005 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03041 | hp2 | a0002 | c0001 | t0001 | g0055 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03098 | hp1 | a0002 | c0001 | t0001 | g0017 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03098 | hp2 | a0002 | c0001 | t0001 | g0026 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03130 | hp1 | a0001 | c0004 | t0002 | g0005 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03130 | hp2 | a0002 | c0001 | t0001 | g0018 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03139 | hp1 | a0001 | c0004 | t0002 | g0005 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03139 | hp2 | a0002 | c0001 | t0001 | g0060 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03195 | hp1 | a0006 | c0009 | t0003 | g0213 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03195 | hp2 | a0002 | c0001 | t0001 | g0063 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03209 | hp1 | a0001 | c0005 | t0002 | g0016 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03209 | hp2 | a0007 | c0016 | t0002 | g0184 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03225 | hp1 | a0001 | c0004 | t0002 | g0005 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03225 | hp2 | a0001 | c0003 | t0003 | g0215 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0174 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03239 | hp2 | a0001 | c0003 | t0003 | g0249 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03453 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03453 | hp2 | a0002 | c0001 | t0001 | g0017 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03486 | hp1 | a0003 | c0006 | t0001 | g0091 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03486 | hp2 | a0002 | c0001 | t0001 | g0066 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03490 | hp1 | a0001 | c0003 | t0003 | g0040 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03490 | hp2 | a0002 | c0001 | t0001 | g0031 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03491 | hp1 | a0002 | c0001 | t0001 | g0122 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0159 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03492 | hp1 | a0002 | c0001 | t0001 | g0031 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03492 | hp2 | a0002 | c0001 | t0001 | g0123 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03516 | hp1 | a0001 | c0005 | t0002 | g0016 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03516 | hp2 | a0002 | c0001 | t0001 | g0070 | AFR | ESN | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03540 | hp1 | a0002 | c0001 | t0001 | g0075 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03540 | hp2 | a0001 | c0004 | t0002 | g0005 | AFR | GWD | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03579 | hp1 | a0001 | c0004 | t0002 | g0005 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03579 | hp2 | a0001 | c0003 | t0003 | g0205 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03654 | hp1 | a0002 | c0001 | t0001 | g0020 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03654 | hp2 | a0001 | c0003 | t0003 | g0239 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03669 | hp1 | a0001 | c0003 | t0003 | g0248 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0151 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0141 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0197 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0156 | SAS | PJL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03831 | hp1 | a0002 | c0001 | t0001 | g0130 | SAS | BEB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | BEB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03834 | hp1 | a0001 | c0003 | t0003 | g0241 | SAS | BEB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03834 | hp2 | a0001 | c0003 | t0003 | g0247 | SAS | BEB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03942 | hp1 | a0001 | c0003 | t0003 | g0041 | SAS | BEB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03942 | hp2 | a0002 | c0001 | t0001 | g0114 | SAS | BEB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0188 | SAS | STU | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG04115 | hp2 | a0001 | c0003 | t0003 | g0226 | SAS | STU | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG04184 | hp1 | a0002 | c0001 | t0001 | g0129 | SAS | BEB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG04204 | hp1 | a0001 | c0003 | t0003 | g0013 | SAS | STU | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG04204 | hp2 | a0002 | c0001 | t0001 | g0020 | SAS | STU | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0007 | SAS | STU | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0021 | SAS | STU | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18522 | hp1 | a0001 | c0004 | t0002 | g0005 | AFR | YRI | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18522 | hp2 | a0002 | c0001 | t0001 | g0092 | AFR | YRI | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | CHB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18612 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | CHB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | CHB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18747 | hp2 | a0002 | c0001 | t0001 | g0118 | EAS | CHB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0183 | AFR | YRI | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18906 | hp2 | a0002 | c0001 | t0001 | g0080 | AFR | YRI | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18940 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18941 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18942 | hp2 | a0001 | c0003 | t0003 | g0225 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18943 | hp1 | a0001 | c0003 | t0003 | g0233 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18946 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18947 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18947 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18949 | hp1 | a0001 | c0003 | t0003 | g0219 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18949 | hp2 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18951 | hp2 | a0001 | c0003 | t0003 | g0203 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18954 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18956 | hp2 | a0001 | c0003 | t0003 | g0222 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18957 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18957 | hp2 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18959 | hp1 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18959 | hp2 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18960 | hp1 | a0001 | c0003 | t0003 | g0204 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18962 | hp2 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18963 | hp1 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18963 | hp2 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18964 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18967 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18967 | hp2 | a0001 | c0003 | t0003 | g0218 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18968 | hp1 | a0001 | c0003 | t0003 | g0245 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18970 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18971 | hp1 | a0002 | c0001 | t0001 | g0119 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18972 | hp1 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18973 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18973 | hp2 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18974 | hp1 | a0001 | c0003 | t0003 | g0037 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18977 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18979 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18981 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18983 | hp1 | a0001 | c0003 | t0003 | g0224 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18984 | hp2 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18985 | hp1 | a0002 | c0001 | t0001 | g0116 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18985 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18986 | hp1 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18987 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18987 | hp2 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18988 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18989 | hp2 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18991 | hp1 | a0001 | c0003 | t0003 | g0244 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18991 | hp2 | a0009 | c0017 | t0002 | g0194 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18992 | hp2 | a0002 | c0001 | t0001 | g0069 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18993 | hp1 | a0001 | c0003 | t0003 | g0227 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18993 | hp2 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18994 | hp1 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18995 | hp1 | a0001 | c0003 | t0003 | g0223 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18995 | hp2 | a0002 | c0001 | t0001 | g0097 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18999 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19000 | hp1 | a0002 | c0001 | t0001 | g0125 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19000 | hp2 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19001 | hp1 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19004 | hp1 | a0002 | c0001 | t0001 | g0044 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19005 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19006 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19006 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19009 | hp1 | a0005 | c0014 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19009 | hp2 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19010 | hp1 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19011 | hp1 | a0001 | c0003 | t0003 | g0041 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19011 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19012 | hp1 | a0002 | c0001 | t0001 | g0098 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19012 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19030 | hp1 | a0001 | c0004 | t0002 | g0199 | AFR | LWK | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19030 | hp2 | a0002 | c0001 | t0001 | g0101 | AFR | LWK | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19043 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | LWK | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19043 | hp2 | a0001 | c0007 | t0001 | g0057 | AFR | LWK | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19054 | hp2 | a0001 | c0003 | t0003 | g0037 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19055 | hp1 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19055 | hp2 | a0002 | c0001 | t0001 | g0096 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19057 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19057 | hp2 | a0001 | c0003 | t0003 | g0217 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19058 | hp1 | a0002 | c0001 | t0001 | g0115 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19058 | hp2 | a0001 | c0003 | t0003 | g0230 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19062 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19063 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19066 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19067 | hp1 | a0001 | c0003 | t0003 | g0234 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19070 | hp2 | a0002 | c0001 | t0001 | g0105 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19072 | hp1 | a0001 | c0003 | t0003 | g0238 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19072 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19075 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19077 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19078 | hp1 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19082 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19083 | hp1 | a0002 | c0008 | t0001 | g0113 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19084 | hp2 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19085 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19086 | hp1 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19089 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19091 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19240 | hp1 | a0002 | c0001 | t0001 | g0076 | AFR | YRI | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA19240 | hp2 | a0001 | c0003 | t0003 | g0208 | AFR | YRI | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA20129 | hp1 | a0003 | c0006 | t0001 | g0028 | AFR | ASW | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ASW | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0187 | EUR | TSI | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0160 | EUR | TSI | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA20805 | hp1 | a0002 | c0001 | t0001 | g0111 | EUR | TSI | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0180 | EUR | TSI | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0144 | SAS | GIH | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA20905 | hp2 | a0002 | c0001 | t0001 | g0014 | SAS | GIH | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01123 | hp1 | a0001 | c0003 | t0003 | g0038 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG01123 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | CLM | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02109 | hp1 | a0002 | c0001 | t0001 | g0010 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02109 | hp2 | a0001 | c0005 | t0002 | g0047 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02486 | hp1 | a0002 | c0001 | t0001 | g0017 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02486 | hp2 | a0001 | c0005 | t0002 | g0046 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02559 | hp1 | a0001 | c0004 | t0002 | g0052 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG02559 | hp2 | a0002 | c0001 | t0001 | g0026 | AFR | ACB | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03471 | hp1 | a0001 | c0003 | t0003 | g0201 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
HG03471 | hp2 | a0002 | c0001 | t0001 | g0010 | AFR | MSL | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA20300 | hp1 | a0002 | c0001 | t0001 | g0007 | AFR | USA | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
NA20300 | hp2 | a0001 | c0005 | t0002 | g0016 | AFR | USA | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0001 | REF | REF | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
homoSapiens_grch38 | hp1 | a0002 | c0001 | t0001 | g0002 | REF | REF | GARS1_chr7_30589878_30639033 | GARS1 | chr7 | 30589878 | 30639033 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30595045
|
C | G | 7 | a0001a0004a0005others(4): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
missense_variant | MODERATE | c.124C>G | p.Pro42Ala | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/17 | 168/2437 | 124/2220 | 42/739 | chr7 | 30595045 | ||
chr7:30595049
|
C | G | 1 | a0009 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.128C>G | p.Pro43Arg | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/17 | 172/2437 | 128/2220 | 43/739 | chr7 | 30595049 | ||
chr7:30595096
|
G | A | 1 | a0008 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.175G>A | p.Gly59Arg | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/17 | 219/2437 | 175/2220 | 59/739 | chr7 | 30595096 | ||
chr7:30609652
|
C | T | 1 | a0004 | 1 | HG01167.hp2 | missense_variant | MODERATE | c.803C>T | p.Thr268Ile | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/17 | 847/2437 | 803/2220 | 268/739 | chr7 | 30609652 | ||
chr7:30616027
|
G | A | 1 | a0003 | 5 | HG02257.hp1 HG02280.hp1 HG02818.hp1 others(2): Show |
missense_variant | MODERATE | c.1163G>A | p.Arg388Gln | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 9/17 | 1207/2437 | 1163/2220 | 388/739 | chr7 | 30616027 | ||
chr7:30621484
|
A | C | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1451A>C | p.Lys484Thr | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 11/17 | 1495/2437 | 1451/2220 | 484/739 | chr7 | 30621484 | ||
chr7:30633843
|
G | C | 1 | a0006 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.2203G>C | p.Glu735Gln | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 17/17 | 2247/2437 | 2203/2220 | 735/739 | chr7 | 30633843 | ||
chr7:30633852
|
G | A | 1 | a0005 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.2212G>A | p.Glu738Lys | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 17/17 | 2256/2437 | 2212/2220 | 738/739 | chr7 | 30633852 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30594966
|
T | G | 1 | a0002c0008 | 1 | NA19083.hp1 | synonymous_variant | LOW | c.45T>G | p.Ala15Ala | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/17 | 89/2437 | 45/2220 | 15/739 | chr7 | 30594966 | ||
chr7:30595014
|
G | C | 3 | a0001c0003a0004c0010a0006c0009 | 81 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(78): Show |
synonymous_variant | LOW | c.93G>C | p.Leu31Leu | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/17 | 137/2437 | 93/2220 | 31/739 | chr7 | 30595014 | ||
chr7:30601144
|
A | G | 1 | a0002c0011 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.513A>G | p.Gln171Gln | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/17 | 557/2437 | 513/2220 | 171/739 | chr7 | 30601144 | ||
chr7:30609596
|
T | C | 1 | a0001c0007 | 5 | HG01069.hp2 HG01071.hp1 HG02647.hp1 others(2): Show |
synonymous_variant | LOW | c.747T>C | p.Tyr249Tyr | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/17 | 791/2437 | 747/2220 | 249/739 | chr7 | 30609596 | ||
chr7:30615926
|
T | C | 2 | a0001c0005a0001c0013 | 8 | HG01891.hp2 HG01978.hp1 HG02109.hp2 others(5): Show |
synonymous_variant | LOW | c.1062T>C | p.Phe354Phe | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 9/17 | 1106/2437 | 1062/2220 | 354/739 | chr7 | 30615926 | ||
chr7:30628621
|
G | A | 1 | a0001c0007 | 5 | HG01069.hp2 HG01071.hp1 HG02647.hp1 others(2): Show |
synonymous_variant | LOW | c.1761G>A | p.Thr587Thr | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/17 | 1805/2437 | 1761/2220 | 587/739 | chr7 | 30628621 | ||
chr7:30631471
|
T | C | 2 | a0001c0005a0001c0013 | 8 | HG01891.hp2 HG01978.hp1 HG02109.hp2 others(5): Show |
synonymous_variant | LOW | c.1833T>C | p.Val611Val | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 15/17 | 1877/2437 | 1833/2220 | 611/739 | chr7 | 30631471 | ||
chr7:30632305
|
C | T | 1 | a0001c0015 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.1962C>T | p.Ile654Ile | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/17 | 2006/2437 | 1962/2220 | 654/739 | chr7 | 30632305 | ||
chr7:30633785
|
A | G | 3 | a0001c0004a0001c0005a0001c0013 | 25 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(22): Show |
synonymous_variant | LOW | c.2145A>G | p.Thr715Thr | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 17/17 | 2189/2437 | 2145/2220 | 715/739 | chr7 | 30633785 | ||
chr7:30633830
|
G | A | 1 | a0001c0013 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.2190G>A | p.Glu730Glu | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 17/17 | 2234/2437 | 2190/2220 | 730/739 | chr7 | 30633830 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30633896
|
TA | T | 10 | a0001c0002t0002a0001c0002t0004a0001c0003t0002others(7): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*51delA | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 17/17 | 51 | INFO_REALIGN_3_PRIME | chr7 | 30633896 | ||||
chr7:30633896
|
TAA | T | 3 | a0001c0003t0003a0004c0010t0003a0006c0009t0003 | 80 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*50_*51delAA | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 17/17 | 50 | INFO_REALIGN_3_PRIME | chr7 | 30633896 | ||||
chr7:30633933
|
A | G | 1 | a0001c0002t0004 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*73A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 17/17 | 73 | chr7 | 30633933 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30595148
|
C | T | 58 | a0001c0003t0002g0240a0001c0003t0003g0006a0001c0003t0003g0012others(55): Show | 81 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(78): Show |
splice_region_variant&intron_variant | LOW | c.222+5C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30595148 | ||||||
chr7:30595166
|
G | C | 1 | a0001c0003t0003g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.222+23G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30595166 | ||||||
chr7:30595591
|
G | A | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.222+448G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30595591 | ||||||
chr7:30595747
|
G | A | 1 | a0001c0002t0002g0043 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.222+604G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30595747 | ||||||
chr7:30595748
|
G | A | 1 | a0001c0002t0002g0043 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.222+605G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30595748 | ||||||
chr7:30595750
|
G | A | 1 | a0001c0002t0002g0043 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.222+607G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30595750 | ||||||
chr7:30595905
|
G | C | 4 | a0001c0003t0003g0012a0001c0003t0003g0202a0001c0003t0003g0203others(1): Show | 8 | NA18951.hp2 NA18957.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+762G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30595905 | ||||||
chr7:30595949
|
A | C | 2 | a0001c0004t0002g0199a0001c0004t0002g0200 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.222+806A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30595949 | ||||||
chr7:30595984
|
C | T | 79 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(76): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.222+841C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30595984 | ||||||
chr7:30596155
|
C | G | 1 | a0001c0003t0003g0249 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.222+1012C>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30596155 | ||||||
chr7:30596405
|
G | T | 1 | a0001c0003t0003g0248 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.222+1262G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30596405 | ||||||
chr7:30596486
|
GA | G | 3 | a0001c0004t0002g0005a0001c0004t0002g0199a0001c0004t0002g0200 | 12 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.222+1354delA | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 30596486 | |||||
chr7:30596497
|
A | C | 1 | a0001c0003t0003g0247 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.222+1354A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30596497 | ||||||
chr7:30596710
|
T | G | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.222+1567T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30596710 | ||||||
chr7:30596784
|
T | A | 1 | a0002c0001t0001g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.222+1641T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30596784 | ||||||
chr7:30596800
|
T | C | 5 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(2): Show | 7 | HG01978.hp1 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+1657T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30596800 | ||||||
chr7:30596830
|
A | G | 2 | a0001c0002t0002g0197a0001c0002t0002g0198 | 2 | HG00735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.222+1687A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30596830 | ||||||
chr7:30596885
|
A | G | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.222+1742A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30596885 | ||||||
chr7:30597171
|
C | T | 5 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(2): Show | 7 | HG01978.hp1 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.223-1625C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30597171 | ||||||
chr7:30597223
|
G | A | 73 | a0001c0002t0004g0042a0001c0003t0002g0240a0001c0003t0003g0006others(70): Show | 107 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.223-1573G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30597223 | ||||||
chr7:30597271
|
G | C | 1 | a0002c0001t0001g0055 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.223-1525G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30597271 | ||||||
chr7:30597423
|
G | A | 1 | a0001c0003t0003g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.223-1373G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30597423 | ||||||
chr7:30597452
|
T | C | 1 | a0001c0004t0002g0005 | 10 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-1344T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30597452 | ||||||
chr7:30598289
|
G | A | 1 | a0002c0001t0001g0017 | 3 | HG02486.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223-507G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30598289 | ||||||
chr7:30598377
|
C | CT | 16 | a0001c0002t0002g0190a0001c0002t0002g0191a0001c0002t0002g0192others(13): Show | 16 | HG00609.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.223-396dupT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 30598377 | |||||
chr7:30598377
|
CT | C | 96 | a0001c0002t0001g0019a0001c0002t0002g0088a0001c0002t0002g0132others(93): Show | 146 | HG00099.hp1 HG00558.hp2 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.223-396delT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 30598377 | |||||
chr7:30598377
|
CTT | C | 19 | a0001c0003t0003g0206a0001c0007t0001g0024a0001c0007t0001g0056others(16): Show | 27 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.223-397_223-396del others(2): Show |
GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 30598377 | |||||
chr7:30598481
|
C | T | 1 | a0001c0003t0003g0241 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.223-315C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30598481 | ||||||
chr7:30598492
|
G | A | 5 | a0001c0004t0002g0005a0001c0004t0002g0049a0001c0004t0002g0050others(2): Show | 14 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.223-304G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30598492 | ||||||
chr7:30598630
|
G | A | 10 | a0002c0001t0001g0003a0002c0001t0001g0068a0002c0001t0001g0069others(7): Show | 18 | HG01928.hp2 HG01934.hp1 HG02273.hp1 others(15): Show |
intron_variant | MODIFIER | c.223-166G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30598630 | ||||||
chr7:30598664
|
G | A | 2 | a0001c0002t0002g0136a0001c0002t0002g0137 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.223-132G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30598664 | ||||||
chr7:30598675
|
C | T | 1 | a0002c0001t0001g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.223-121C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30598675 | ||||||
chr7:30598676
|
G | A | 15 | a0001c0002t0004g0042a0001c0004t0002g0005a0001c0004t0002g0049others(12): Show | 26 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.223-120G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 1/16 | chr7 | 30598676 | ||||||
chr7:30599031
|
C | A | 8 | a0002c0001t0001g0014a0002c0001t0001g0029a0002c0001t0001g0096others(5): Show | 12 | HG00408.hp2 NA18942.hp1 NA18963.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+134C>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 2/16 | chr7 | 30599031 | ||||||
chr7:30599112
|
C | T | 2 | a0001c0004t0002g0049a0001c0004t0002g0050 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.324+215C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 2/16 | chr7 | 30599112 | ||||||
chr7:30599156
|
T | G | 12 | a0001c0004t0002g0005a0001c0004t0002g0049a0001c0004t0002g0050others(9): Show | 23 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.324+259T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 2/16 | chr7 | 30599156 | ||||||
chr7:30599261
|
C | T | 1 | a0002c0001t0001g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.324+364C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 2/16 | chr7 | 30599261 | ||||||
chr7:30599489
|
G | C | 1 | a0001c0002t0002g0138 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.325-458G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 2/16 | chr7 | 30599489 | ||||||
chr7:30599655
|
G | T | 1 | a0001c0002t0002g0189 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.325-292G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 2/16 | chr7 | 30599655 | ||||||
chr7:30599656
|
G | A | 2 | a0001c0002t0002g0139a0001c0002t0002g0140 | 2 | NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.325-291G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 2/16 | chr7 | 30599656 | ||||||
chr7:30599783
|
G | A | 1 | a0001c0002t0002g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.325-164G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 2/16 | chr7 | 30599783 | ||||||
chr7:30599885
|
T | C | 1 | a0002c0001t0001g0129 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.325-62T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 2/16 | chr7 | 30599885 | ||||||
chr7:30599913
|
T | C | 1 | a0002c0001t0001g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.325-34T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 2/16 | chr7 | 30599913 | ||||||
chr7:30600225
|
C | G | 49 | a0001c0003t0002g0240a0001c0003t0003g0006a0001c0003t0003g0012others(46): Show | 72 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.427+176C>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 3/16 | chr7 | 30600225 | ||||||
chr7:30600270
|
T | C | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.427+221T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 3/16 | chr7 | 30600270 | ||||||
chr7:30600359
|
A | G | 1 | a0003c0006t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.427+310A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 3/16 | chr7 | 30600359 | ||||||
chr7:30600472
|
C | A | 1 | a0001c0002t0002g0132 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.427+423C>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 3/16 | chr7 | 30600472 | ||||||
chr7:30600739
|
G | T | 73 | a0001c0002t0004g0042a0001c0003t0002g0240a0001c0003t0003g0006others(70): Show | 107 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.428-320G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 3/16 | chr7 | 30600739 | ||||||
chr7:30600765
|
C | T | 1 | a0002c0001t0001g0090 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.428-294C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 3/16 | chr7 | 30600765 | ||||||
chr7:30600882
|
CT | C | 4 | a0001c0007t0001g0024a0001c0007t0001g0056a0001c0007t0001g0057others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-171delT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 30600882 | |||||
chr7:30600899
|
C | T | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.428-160C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 3/16 | chr7 | 30600899 | ||||||
chr7:30600920
|
G | A | 13 | a0002c0001t0001g0025a0002c0001t0001g0026a0002c0001t0001g0027others(10): Show | 16 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.428-139G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 3/16 | chr7 | 30600920 | ||||||
chr7:30601028
|
A | G | 1 | a0001c0003t0003g0246 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.428-31A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 3/16 | chr7 | 30601028 | ||||||
chr7:30601373
|
T | C | 23 | a0001c0002t0004g0042a0001c0004t0002g0005a0001c0004t0002g0049others(20): Show | 38 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.569+173T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30601373 | ||||||
chr7:30601683
|
C | T | 6 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(3): Show | 8 | HG01891.hp2 HG01978.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+483C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30601683 | ||||||
chr7:30601684
|
T | G | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.569+484T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30601684 | ||||||
chr7:30601898
|
C | G | 2 | a0001c0002t0002g0188a0001c0002t0002g0196 | 2 | HG00735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.569+698C>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30601898 | ||||||
chr7:30601944
|
A | G | 8 | a0002c0001t0001g0014a0002c0001t0001g0029a0002c0001t0001g0096others(5): Show | 12 | HG00408.hp2 NA18942.hp1 NA18963.hp2 others(9): Show |
intron_variant | MODIFIER | c.569+744A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30601944 | ||||||
chr7:30602119
|
C | T | 1 | a0001c0002t0002g0187 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.570-915C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30602119 | ||||||
chr7:30602181
|
C | T | 1 | a0002c0001t0001g0076 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.570-853C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30602181 | ||||||
chr7:30602233
|
C | T | 1 | a0001c0002t0002g0186 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.570-801C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30602233 | ||||||
chr7:30602356
|
C | T | 1 | a0002c0001t0001g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.570-678C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30602356 | ||||||
chr7:30602372
|
C | T | 14 | a0001c0004t0002g0005a0001c0004t0002g0049a0001c0004t0002g0050others(11): Show | 25 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.570-662C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30602372 | ||||||
chr7:30602418
|
A | G | 8 | a0002c0001t0001g0010a0002c0001t0001g0066a0002c0001t0001g0071others(5): Show | 12 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.570-616A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30602418 | ||||||
chr7:30602490
|
A | G | 80 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(77): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.570-544A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30602490 | ||||||
chr7:30602716
|
A | G | 1 | a0001c0004t0002g0005 | 10 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.570-318A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30602716 | ||||||
chr7:30602883
|
C | A | 192 | a0001c0002t0001g0019a0001c0002t0002g0001a0001c0002t0002g0009others(189): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.570-151C>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | chr7 | 30602883 | ||||||
chr7:30602961
|
ATTATC | A | 13 | a0002c0001t0001g0025a0002c0001t0001g0026a0002c0001t0001g0027others(10): Show | 16 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.570-68_570-64delCT others(3): Show |
GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr7 | 30602961 | |||||
chr7:30603258
|
T | C | 1 | a0002c0001t0001g0102 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.658+136T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 5/16 | chr7 | 30603258 | ||||||
chr7:30603453
|
C | A | 78 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(75): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.659-43C>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 5/16 | chr7 | 30603453 | ||||||
chr7:30603636
|
A | G | 2 | a0001c0002t0002g0183a0007c0016t0002g0184 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.735+64A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30603636 | ||||||
chr7:30603665
|
C | A | 2 | a0001c0003t0003g0207a0001c0003t0003g0242 | 2 | HG01099.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.735+93C>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30603665 | ||||||
chr7:30603675
|
T | C | 1 | a0001c0002t0002g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.735+103T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30603675 | ||||||
chr7:30603914
|
T | G | 1 | a0002c0001t0001g0025 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.735+342T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30603914 | ||||||
chr7:30604132
|
T | C | 58 | a0001c0003t0002g0240a0001c0003t0003g0006a0001c0003t0003g0012others(55): Show | 81 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.735+560T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30604132 | ||||||
chr7:30604430
|
A | ATC | 3 | a0001c0004t0002g0051a0001c0004t0002g0052a0001c0004t0002g0053 | 3 | HG01081.hp2 HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.735+874_735+875dup others(2): Show |
GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 30604430 | |||||
chr7:30604485
|
G | A | 1 | a0002c0001t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.735+913G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30604485 | ||||||
chr7:30604519
|
A | AT | 58 | a0001c0003t0002g0240a0001c0003t0003g0006a0001c0003t0003g0012others(55): Show | 81 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.735+957dupT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 30604519 | |||||
chr7:30604557
|
A | G | 1 | a0002c0001t0001g0033 | 2 | HG00558.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.735+985A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30604557 | ||||||
chr7:30604602
|
T | C | 5 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(2): Show | 7 | HG01978.hp1 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+1030T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30604602 | ||||||
chr7:30604650
|
A | T | 5 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(2): Show | 7 | HG01978.hp1 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+1078A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30604650 | ||||||
chr7:30604688
|
C | T | 1 | a0001c0002t0002g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.735+1116C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30604688 | ||||||
chr7:30605046
|
A | G | 5 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(2): Show | 7 | HG01978.hp1 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+1474A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30605046 | ||||||
chr7:30605175
|
A | G | 1 | a0001c0004t0002g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.735+1603A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30605175 | ||||||
chr7:30605333
|
C | T | 79 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(76): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.735+1761C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30605333 | ||||||
chr7:30605581
|
G | T | 1 | a0001c0003t0002g0240 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.735+2009G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30605581 | ||||||
chr7:30605586
|
T | C | 5 | a0001c0004t0002g0005a0001c0004t0002g0049a0001c0004t0002g0050others(2): Show | 14 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.735+2014T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30605586 | ||||||
chr7:30605607
|
T | C | 1 | a0001c0004t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.735+2035T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30605607 | ||||||
chr7:30605677
|
C | G | 1 | a0002c0001t0001g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.735+2105C>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30605677 | ||||||
chr7:30605712
|
A | G | 1 | a0002c0001t0001g0131 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.735+2140A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30605712 | ||||||
chr7:30605979
|
C | T | 1 | a0001c0003t0003g0239 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.735+2407C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30605979 | ||||||
chr7:30605994
|
C | T | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.735+2422C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30605994 | ||||||
chr7:30606001
|
G | A | 3 | a0001c0003t0003g0214a0001c0003t0003g0215a0006c0009t0003g0213 | 3 | HG02976.hp2 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.735+2429G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606001 | ||||||
chr7:30606020
|
T | C | 8 | a0001c0004t0002g0005a0001c0004t0002g0049a0001c0004t0002g0050others(5): Show | 17 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.735+2448T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606020 | ||||||
chr7:30606112
|
T | G | 1 | a0001c0003t0003g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.735+2540T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606112 | ||||||
chr7:30606123
|
A | G | 1 | a0001c0002t0002g0181 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.735+2551A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606123 | ||||||
chr7:30606156
|
G | A | 2 | a0001c0004t0002g0052a0001c0004t0002g0053 | 2 | HG01081.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.735+2584G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606156 | ||||||
chr7:30606252
|
G | C | 5 | a0001c0004t0002g0005a0001c0004t0002g0049a0001c0004t0002g0050others(2): Show | 14 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.735+2680G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606252 | ||||||
chr7:30606305
|
C | CT | 140 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(137): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.735+2751dupT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 30606305 | |||||
chr7:30606305
|
CT | C | 7 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(4): Show | 9 | HG01978.hp1 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.735+2751delT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr7 | 30606305 | |||||
chr7:30606561
|
T | A | 26 | a0001c0007t0001g0024a0001c0007t0001g0056a0001c0007t0001g0057others(23): Show | 33 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.735+2989T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606561 | ||||||
chr7:30606736
|
C | A | 1 | a0001c0002t0002g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.736-2849C>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606736 | ||||||
chr7:30606756
|
G | A | 80 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(77): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.736-2829G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606756 | ||||||
chr7:30606757
|
T | C | 2 | a0001c0002t0002g0145a0001c0002t0002g0146 | 2 | NA18988.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.736-2828T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606757 | ||||||
chr7:30606820
|
A | G | 1 | a0001c0004t0002g0005 | 10 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.736-2765A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30606820 | ||||||
chr7:30607163
|
C | G | 5 | a0002c0001t0001g0018a0002c0001t0001g0077a0002c0001t0001g0080others(2): Show | 7 | HG02257.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.736-2422C>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607163 | ||||||
chr7:30607297
|
C | T | 1 | a0001c0002t0002g0180 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.736-2288C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607297 | ||||||
chr7:30607301
|
T | C | 160 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(157): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.736-2284T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607301 | ||||||
chr7:30607302
|
G | A | 2 | a0001c0004t0002g0199a0001c0004t0002g0200 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.736-2283G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607302 | ||||||
chr7:30607514
|
A | G | 1 | a0002c0001t0001g0017 | 3 | HG02486.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.736-2071A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607514 | ||||||
chr7:30607521
|
G | A | 1 | a0001c0004t0002g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.736-2064G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607521 | ||||||
chr7:30607578
|
A | G | 1 | a0001c0003t0003g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.736-2007A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607578 | ||||||
chr7:30607603
|
G | C | 1 | a0002c0001t0001g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.736-1982G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607603 | ||||||
chr7:30607688
|
A | G | 8 | a0002c0001t0001g0010a0002c0001t0001g0066a0002c0001t0001g0071others(5): Show | 12 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.736-1897A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607688 | ||||||
chr7:30607835
|
G | A | 13 | a0002c0001t0001g0025a0002c0001t0001g0026a0002c0001t0001g0027others(10): Show | 16 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.736-1750G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607835 | ||||||
chr7:30607884
|
A | G | 58 | a0001c0003t0002g0240a0001c0003t0003g0006a0001c0003t0003g0012others(55): Show | 81 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.736-1701A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30607884 | ||||||
chr7:30608137
|
A | G | 1 | a0001c0002t0002g0179 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.736-1448A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30608137 | ||||||
chr7:30608435
|
G | A | 81 | a0001c0002t0004g0042a0001c0003t0002g0240a0001c0003t0003g0006others(78): Show | 119 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(116): Show |
intron_variant | MODIFIER | c.736-1150G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30608435 | ||||||
chr7:30608492
|
A | T | 1 | a0001c0003t0003g0238 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.736-1093A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30608492 | ||||||
chr7:30608493
|
T | A | 1 | a0001c0003t0003g0238 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.736-1092T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30608493 | ||||||
chr7:30608495
|
A | T | 1 | a0001c0003t0003g0238 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.736-1090A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30608495 | ||||||
chr7:30608569
|
T | C | 3 | a0001c0004t0002g0051a0001c0004t0002g0052a0001c0004t0002g0053 | 3 | HG01081.hp2 HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.736-1016T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30608569 | ||||||
chr7:30608657
|
T | C | 1 | a0002c0001t0001g0096 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.736-928T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30608657 | ||||||
chr7:30608677
|
A | G | 1 | a0001c0003t0003g0239 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.736-908A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30608677 | ||||||
chr7:30608682
|
G | A | 1 | a0001c0002t0002g0147 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.736-903G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30608682 | ||||||
chr7:30608864
|
C | T | 1 | a0001c0003t0003g0204 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.736-721C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30608864 | ||||||
chr7:30609003
|
T | A | 3 | a0001c0003t0003g0037a0001c0003t0003g0219a0001c0003t0003g0238 | 4 | NA18949.hp1 NA18974.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-582T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30609003 | ||||||
chr7:30609164
|
G | T | 1 | a0002c0001t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.736-421G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30609164 | ||||||
chr7:30609267
|
C | T | 1 | a0001c0002t0002g0178 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.736-318C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 6/16 | chr7 | 30609267 | ||||||
chr7:30609800
|
T | C | 1 | a0001c0002t0001g0019 | 3 | HG02622.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.881+70T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30609800 | ||||||
chr7:30609869
|
A | T | 1 | a0001c0004t0002g0053 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.881+139A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30609869 | ||||||
chr7:30609970
|
A | G | 1 | a0001c0002t0002g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.881+240A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30609970 | ||||||
chr7:30610094
|
A | T | 1 | a0002c0001t0001g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.881+364A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30610094 | ||||||
chr7:30610281
|
T | C | 2 | a0002c0001t0001g0030a0002c0001t0001g0104 | 3 | HG00544.hp1 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.881+551T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30610281 | ||||||
chr7:30610442
|
A | G | 1 | a0001c0002t0002g0176 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.881+712A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30610442 | ||||||
chr7:30610753
|
G | A | 20 | a0002c0001t0001g0003a0002c0001t0001g0004a0002c0001t0001g0033others(17): Show | 38 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.881+1023G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30610753 | ||||||
chr7:30610802
|
A | G | 1 | a0001c0004t0002g0053 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.881+1072A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30610802 | ||||||
chr7:30611147
|
T | C | 1 | a0001c0003t0003g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.882-949T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30611147 | ||||||
chr7:30611247
|
A | G | 2 | a0002c0001t0001g0122a0002c0001t0001g0123 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.882-849A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30611247 | ||||||
chr7:30611514
|
C | T | 3 | a0001c0002t0002g0175a0001c0002t0002g0176a0001c0002t0002g0195 | 3 | NA18940.hp2 NA18941.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.882-582C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30611514 | ||||||
chr7:30611554
|
G | A | 1 | a0001c0002t0002g0197 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.882-542G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30611554 | ||||||
chr7:30611727
|
G | A | 1 | a0001c0004t0002g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.882-369G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30611727 | ||||||
chr7:30611769
|
C | T | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.882-327C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30611769 | ||||||
chr7:30611778
|
G | A | 1 | a0001c0002t0002g0148 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.882-318G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30611778 | ||||||
chr7:30612004
|
T | A | 1 | a0001c0003t0003g0238 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.882-92T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 7/16 | chr7 | 30612004 | ||||||
chr7:30612322
|
G | A | 188 | a0001c0002t0001g0019a0001c0002t0002g0001a0001c0002t0002g0009others(185): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1031+77G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30612322 | ||||||
chr7:30612474
|
C | T | 7 | a0001c0002t0002g0011a0001c0002t0002g0036a0001c0002t0002g0132others(4): Show | 11 | HG00609.hp2 HG00639.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1031+229C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30612474 | ||||||
chr7:30612512
|
T | C | 1 | a0002c0001t0001g0059 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1031+267T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30612512 | ||||||
chr7:30612545
|
A | T | 1 | a0001c0003t0003g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1031+300A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30612545 | ||||||
chr7:30612653
|
C | G | 1 | a0002c0001t0001g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1031+408C>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30612653 | ||||||
chr7:30612789
|
C | T | 66 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(63): Show | 108 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1031+544C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30612789 | ||||||
chr7:30613082
|
C | T | 1 | a0001c0002t0002g0195 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1031+837C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30613082 | ||||||
chr7:30613096
|
A | G | 5 | a0001c0002t0001g0019a0003c0006t0001g0028a0003c0006t0001g0078others(2): Show | 8 | HG02257.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1031+851A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30613096 | ||||||
chr7:30613239
|
G | A | 1 | a0001c0003t0003g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1031+994G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30613239 | ||||||
chr7:30613324
|
G | C | 1 | a0001c0005t0002g0045 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1031+1079G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30613324 | ||||||
chr7:30613334
|
A | G | 1 | a0001c0004t0002g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1031+1089A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30613334 | ||||||
chr7:30613623
|
T | C | 6 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(3): Show | 8 | HG01891.hp2 HG01978.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031+1378T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30613623 | ||||||
chr7:30613686
|
T | C | 1 | a0001c0002t0002g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1031+1441T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30613686 | ||||||
chr7:30614196
|
C | A | 1 | a0001c0005t0002g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1032-1700C>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614196 | ||||||
chr7:30614228
|
CT | C | 4 | a0002c0001t0001g0018a0002c0001t0001g0080a0002c0001t0001g0081others(1): Show | 6 | HG02257.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1032-1655delT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 30614228 | |||||
chr7:30614245
|
G | A | 1 | a0001c0002t0002g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1032-1651G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614245 | ||||||
chr7:30614441
|
A | G | 2 | a0001c0004t0002g0052a0001c0004t0002g0053 | 2 | HG01081.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1032-1455A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614441 | ||||||
chr7:30614447
|
G | C | 1 | a0001c0002t0002g0149 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1032-1449G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614447 | ||||||
chr7:30614491
|
A | G | 71 | a0001c0002t0004g0042a0001c0003t0002g0240a0001c0003t0003g0006others(68): Show | 105 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.1032-1405A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614491 | ||||||
chr7:30614514
|
G | A | 6 | a0001c0004t0002g0005a0001c0004t0002g0049a0001c0004t0002g0050others(3): Show | 15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1032-1382G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614514 | ||||||
chr7:30614530
|
A | G | 1 | a0001c0002t0002g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1032-1366A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614530 | ||||||
chr7:30614602
|
G | A | 1 | a0002c0001t0001g0105 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1032-1294G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614602 | ||||||
chr7:30614604
|
A | G | 15 | a0001c0002t0004g0042a0001c0004t0002g0005a0001c0004t0002g0049others(12): Show | 26 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1032-1292A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614604 | ||||||
chr7:30614688
|
A | G | 3 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237 | 3 | HG00738.hp1 HG01081.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1032-1208A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614688 | ||||||
chr7:30614727
|
T | G | 1 | a0002c0001t0001g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1032-1169T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614727 | ||||||
chr7:30614800
|
C | T | 3 | a0001c0003t0003g0040a0001c0003t0003g0233a0001c0003t0003g0234 | 4 | HG00558.hp2 HG03490.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032-1096C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614800 | ||||||
chr7:30614853
|
G | A | 1 | a0002c0001t0001g0097 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1032-1043G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30614853 | ||||||
chr7:30614871
|
C | CA | 63 | a0001c0002t0002g0150a0001c0002t0002g0153a0001c0002t0002g0154others(60): Show | 89 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1032-1006dupA | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 30614871 | |||||
chr7:30614871
|
C | CAA | 13 | a0001c0003t0002g0240a0001c0003t0003g0208a0001c0003t0003g0222others(10): Show | 17 | HG01192.hp1 HG01891.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1032-1007_1032-100 others(6): Show |
GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 30614871 | |||||
chr7:30614871
|
CA | C | 7 | a0001c0002t0002g0141a0001c0002t0002g0143a0001c0002t0002g0173others(4): Show | 7 | HG01069.hp1 HG01169.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032-1006delA | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr7 | 30614871 | |||||
chr7:30615061
|
G | A | 1 | a0001c0002t0002g0149 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1032-835G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615061 | ||||||
chr7:30615115
|
G | A | 1 | a0002c0001t0001g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1032-781G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615115 | ||||||
chr7:30615126
|
C | T | 1 | a0001c0004t0002g0053 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1032-770C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615126 | ||||||
chr7:30615127
|
G | A | 1 | a0001c0005t0002g0016 | 3 | HG03209.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1032-769G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615127 | ||||||
chr7:30615218
|
A | G | 1 | a0002c0001t0001g0106 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1032-678A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615218 | ||||||
chr7:30615239
|
A | G | 4 | a0003c0006t0001g0028a0003c0006t0001g0078a0003c0006t0001g0079others(1): Show | 5 | HG02257.hp1 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032-657A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615239 | ||||||
chr7:30615611
|
A | G | 2 | a0002c0001t0001g0063a0002c0001t0001g0064 | 2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1032-285A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615611 | ||||||
chr7:30615676
|
A | T | 1 | a0002c0001t0001g0033 | 2 | HG00558.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1032-220A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615676 | ||||||
chr7:30615747
|
A | T | 5 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(2): Show | 7 | HG01978.hp1 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032-149A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615747 | ||||||
chr7:30615778
|
C | T | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1032-118C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615778 | ||||||
chr7:30615832
|
T | A | 1 | a0001c0005t0002g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1032-64T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615832 | ||||||
chr7:30615873
|
A | T | 54 | a0001c0003t0002g0240a0001c0003t0003g0006a0001c0003t0003g0012others(51): Show | 77 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1032-23A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 8/16 | chr7 | 30615873 | ||||||
chr7:30616270
|
C | G | 1 | a0001c0004t0002g0005 | 10 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1194+212C>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 9/16 | chr7 | 30616270 | ||||||
chr7:30616281
|
A | C | 1 | a0001c0002t0002g0178 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194+223A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 9/16 | chr7 | 30616281 | ||||||
chr7:30616396
|
A | T | 1 | a0001c0003t0003g0232 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1194+338A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 9/16 | chr7 | 30616396 | ||||||
chr7:30616400
|
G | A | 1 | a0001c0002t0002g0155 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1194+342G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 9/16 | chr7 | 30616400 | ||||||
chr7:30616811
|
T | A | 1 | a0001c0002t0002g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1195-303T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 9/16 | chr7 | 30616811 | ||||||
chr7:30617034
|
G | A | 13 | a0001c0002t0002g0021a0001c0002t0002g0136a0001c0002t0002g0137others(10): Show | 15 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.1195-80G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 9/16 | chr7 | 30617034 | ||||||
chr7:30617067
|
T | C | 1 | a0001c0003t0003g0246 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1195-47T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 9/16 | chr7 | 30617067 | ||||||
chr7:30617375
|
A | G | 17 | a0001c0003t0003g0006a0001c0003t0003g0037a0001c0003t0003g0039others(14): Show | 28 | HG00609.hp1 HG00673.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1359+97A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30617375 | ||||||
chr7:30617416
|
A | G | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1359+138A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30617416 | ||||||
chr7:30617466
|
G | A | 1 | a0001c0002t0002g0173 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1359+188G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30617466 | ||||||
chr7:30617531
|
C | T | 1 | a0001c0004t0002g0200 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1359+253C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30617531 | ||||||
chr7:30617577
|
A | G | 81 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(78): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1359+299A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30617577 | ||||||
chr7:30617652
|
A | G | 32 | a0001c0003t0003g0205a0002c0001t0001g0010a0002c0001t0001g0017others(29): Show | 44 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1359+374A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30617652 | ||||||
chr7:30617676
|
A | C | 1 | a0002c0001t0001g0064 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1359+398A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30617676 | ||||||
chr7:30617794
|
C | A | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1359+516C>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30617794 | ||||||
chr7:30617851
|
C | T | 55 | a0001c0003t0003g0006a0001c0003t0003g0012a0001c0003t0003g0013others(52): Show | 78 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.1359+573C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30617851 | ||||||
chr7:30618286
|
C | T | 1 | a0002c0001t0001g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1359+1008C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618286 | ||||||
chr7:30618486
|
T | C | 15 | a0001c0002t0004g0042a0001c0004t0002g0005a0001c0004t0002g0049others(12): Show | 26 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1359+1208T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618486 | ||||||
chr7:30618508
|
C | T | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1359+1230C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618508 | ||||||
chr7:30618618
|
A | G | 1 | a0001c0002t0002g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1359+1340A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618618 | ||||||
chr7:30618645
|
C | T | 1 | a0002c0001t0001g0121 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1359+1367C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618645 | ||||||
chr7:30618757
|
T | A | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+1479T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618757 | ||||||
chr7:30618762
|
A | C | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+1484A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618762 | ||||||
chr7:30618784
|
T | G | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+1506T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618784 | ||||||
chr7:30618840
|
A | G | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+1562A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618840 | ||||||
chr7:30618841
|
T | A | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+1563T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618841 | ||||||
chr7:30618890
|
T | A | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+1612T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618890 | ||||||
chr7:30618977
|
T | G | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+1699T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618977 | ||||||
chr7:30618978
|
G | T | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+1700G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618978 | ||||||
chr7:30618980
|
T | G | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+1702T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30618980 | ||||||
chr7:30619058
|
C | G | 1 | a0002c0001t0001g0129 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1359+1780C>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619058 | ||||||
chr7:30619073
|
A | C | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1359+1795A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619073 | ||||||
chr7:30619084
|
T | A | 1 | a0002c0001t0001g0083 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1359+1806T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619084 | ||||||
chr7:30619290
|
C | T | 1 | a0002c0001t0001g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1359+2012C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619290 | ||||||
chr7:30619343
|
G | A | 2 | a0001c0002t0002g0157a0001c0002t0002g0190 | 2 | HG01192.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1360-2050G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619343 | ||||||
chr7:30619469
|
A | G | 2 | a0002c0001t0001g0120a0002c0001t0001g0121 | 2 | HG00438.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1360-1924A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619469 | ||||||
chr7:30619483
|
A | G | 15 | a0001c0002t0004g0042a0001c0004t0002g0005a0001c0004t0002g0049others(12): Show | 26 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1360-1910A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619483 | ||||||
chr7:30619488
|
C | T | 1 | a0002c0001t0001g0032 | 2 | HG00280.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1360-1905C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619488 | ||||||
chr7:30619509
|
C | T | 7 | a0001c0002t0004g0042a0001c0005t0002g0016a0001c0005t0002g0045others(4): Show | 9 | HG01891.hp2 HG01978.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360-1884C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619509 | ||||||
chr7:30619633
|
T | G | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1360-1760T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619633 | ||||||
chr7:30619707
|
G | A | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1360-1686G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619707 | ||||||
chr7:30619721
|
A | G | 1 | a0002c0001t0001g0017 | 3 | HG02486.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1360-1672A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619721 | ||||||
chr7:30619730
|
A | G | 1 | a0001c0007t0001g0058 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1360-1663A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619730 | ||||||
chr7:30619776
|
C | CT | 17 | a0001c0002t0002g0035a0001c0002t0002g0150a0001c0002t0002g0170others(14): Show | 28 | HG01109.hp1 HG01433.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1360-1598dupT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 30619776 | |||||
chr7:30619776
|
CT | C | 55 | a0001c0002t0002g0133a0001c0002t0004g0042a0001c0003t0003g0006others(52): Show | 79 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1360-1598delT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 30619776 | |||||
chr7:30619780
|
T | A | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1360-1613T>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619780 | ||||||
chr7:30619781
|
T | C | 1 | a0002c0001t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1360-1612T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619781 | ||||||
chr7:30619809
|
A | G | 1 | a0001c0002t0001g0019 | 3 | HG02622.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1360-1584A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619809 | ||||||
chr7:30619934
|
C | T | 81 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(78): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1360-1459C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30619934 | ||||||
chr7:30620128
|
CA | C | 187 | a0001c0002t0001g0019a0001c0002t0002g0001a0001c0002t0002g0009others(184): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1360-1253delA | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 30620128 | |||||
chr7:30620129
|
A | C | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1360-1264A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30620129 | ||||||
chr7:30620217
|
C | T | 1 | a0001c0002t0002g0148 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1360-1176C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30620217 | ||||||
chr7:30620345
|
A | G | 14 | a0001c0003t0003g0205a0002c0001t0001g0025a0002c0001t0001g0026others(11): Show | 17 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1360-1048A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30620345 | ||||||
chr7:30620348
|
G | A | 1 | a0002c0001t0001g0029 | 2 | HG00408.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1360-1045G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30620348 | ||||||
chr7:30620545
|
G | A | 1 | a0002c0001t0001g0084 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1360-848G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30620545 | ||||||
chr7:30620624
|
T | G | 1 | a0001c0002t0002g0133 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1360-769T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30620624 | ||||||
chr7:30620661
|
A | G | 5 | a0001c0004t0002g0005a0001c0004t0002g0049a0001c0004t0002g0050others(2): Show | 14 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360-732A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30620661 | ||||||
chr7:30620801
|
G | A | 1 | a0002c0001t0001g0059 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1360-592G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30620801 | ||||||
chr7:30621046
|
TTTTC | T | 5 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(2): Show | 7 | HG01978.hp1 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1360-339_1360-336d others(6): Show |
GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 30621046 | |||||
chr7:30621054
|
CT | C | 13 | a0001c0002t0002g0132a0001c0002t0002g0139a0001c0002t0002g0158others(10): Show | 13 | HG01070.hp2 HG01169.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1360-322delT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 30621054 | |||||
chr7:30621058
|
T | C | 5 | a0001c0007t0001g0024a0001c0007t0001g0056a0001c0007t0001g0057others(2): Show | 7 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1360-335T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30621058 | ||||||
chr7:30621126
|
G | C | 1 | a0001c0002t0002g0160 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1360-267G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30621126 | ||||||
chr7:30621208
|
A | T | 1 | a0001c0002t0002g0149 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1360-185A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30621208 | ||||||
chr7:30621278
|
T | C | 1 | a0001c0002t0002g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1360-115T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30621278 | ||||||
chr7:30621322
|
A | C | 66 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(63): Show | 108 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1360-71A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 10/16 | chr7 | 30621322 | ||||||
chr7:30621613
|
G | A | 1 | a0002c0001t0001g0008 | 6 | HG01109.hp2 HG02145.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1467+113G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 11/16 | chr7 | 30621613 | ||||||
chr7:30621621
|
G | A | 1 | a0002c0001t0001g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1467+121G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 11/16 | chr7 | 30621621 | ||||||
chr7:30621810
|
C | T | 1 | a0001c0007t0001g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1467+310C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 11/16 | chr7 | 30621810 | ||||||
chr7:30621814
|
C | T | 1 | a0001c0003t0003g0228 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1467+314C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 11/16 | chr7 | 30621814 | ||||||
chr7:30621830
|
A | C | 7 | a0001c0002t0004g0042a0001c0005t0002g0016a0001c0005t0002g0045others(4): Show | 9 | HG01891.hp2 HG01978.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1467+330A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 11/16 | chr7 | 30621830 | ||||||
chr7:30621884
|
C | T | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1467+384C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 11/16 | chr7 | 30621884 | ||||||
chr7:30622032
|
T | C | 57 | a0001c0003t0003g0006a0001c0003t0003g0012a0001c0003t0003g0013others(54): Show | 80 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.1468-285T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 11/16 | chr7 | 30622032 | ||||||
chr7:30622471
|
T | C | 7 | a0001c0002t0004g0042a0001c0005t0002g0016a0001c0005t0002g0045others(4): Show | 9 | HG01891.hp2 HG01978.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1613+9T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30622471 | ||||||
chr7:30622558
|
C | T | 7 | a0001c0002t0004g0042a0001c0005t0002g0016a0001c0005t0002g0045others(4): Show | 9 | HG01891.hp2 HG01978.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1613+96C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30622558 | ||||||
chr7:30622560
|
G | A | 1 | a0001c0002t0002g0148 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1613+98G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30622560 | ||||||
chr7:30622621
|
G | A | 81 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(78): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1613+159G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30622621 | ||||||
chr7:30622732
|
A | G | 1 | a0002c0001t0001g0119 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1613+270A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30622732 | ||||||
chr7:30622782
|
C | T | 1 | a0001c0003t0003g0023 | 3 | NA18972.hp1 NA18986.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1613+320C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30622782 | ||||||
chr7:30622830
|
G | A | 13 | a0002c0001t0001g0025a0002c0001t0001g0026a0002c0001t0001g0027others(10): Show | 16 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1613+368G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30622830 | ||||||
chr7:30622858
|
T | C | 1 | a0001c0003t0002g0240 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1613+396T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30622858 | ||||||
chr7:30622928
|
G | A | 1 | a0001c0002t0002g0132 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1613+466G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30622928 | ||||||
chr7:30623083
|
A | G | 1 | a0001c0003t0003g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1613+621A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623083 | ||||||
chr7:30623095
|
C | T | 1 | a0007c0016t0002g0184 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1613+633C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623095 | ||||||
chr7:30623100
|
C | CA | 15 | a0001c0002t0002g0195a0001c0004t0002g0052a0002c0001t0001g0025others(12): Show | 18 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.1613+651dupA | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 30623100 | |||||
chr7:30623114
|
C | A | 2 | a0001c0004t0002g0199a0002c0008t0001g0113 | 2 | NA19030.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1613+652C>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623114 | ||||||
chr7:30623114
|
C | CA | 6 | a0001c0002t0002g0141a0001c0004t0002g0005a0001c0004t0002g0049others(3): Show | 15 | HG01109.hp1 HG01169.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1613+664dupA | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 30623114 | |||||
chr7:30623132
|
A | G | 3 | a0001c0004t0002g0051a0001c0004t0002g0052a0001c0004t0002g0053 | 3 | HG01081.hp2 HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1613+670A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623132 | ||||||
chr7:30623209
|
T | C | 4 | a0002c0001t0001g0018a0002c0001t0001g0080a0002c0001t0001g0081others(1): Show | 6 | HG02257.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1613+747T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623209 | ||||||
chr7:30623287
|
A | G | 1 | a0001c0003t0003g0227 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1613+825A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623287 | ||||||
chr7:30623317
|
T | C | 3 | a0001c0004t0002g0005a0001c0004t0002g0199a0001c0004t0002g0200 | 12 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1613+855T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623317 | ||||||
chr7:30623346
|
G | A | 1 | a0001c0004t0002g0200 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1613+884G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623346 | ||||||
chr7:30623520
|
A | G | 8 | a0001c0004t0002g0005a0001c0004t0002g0049a0001c0004t0002g0050others(5): Show | 17 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1613+1058A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623520 | ||||||
chr7:30623598
|
C | T | 4 | a0002c0001t0001g0018a0002c0001t0001g0080a0002c0001t0001g0081others(1): Show | 6 | HG02257.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1613+1136C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623598 | ||||||
chr7:30623620
|
T | C | 1 | a0001c0002t0002g0161 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1613+1158T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623620 | ||||||
chr7:30623661
|
T | C | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1613+1199T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623661 | ||||||
chr7:30623807
|
G | T | 1 | a0001c0002t0002g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1613+1345G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30623807 | ||||||
chr7:30624109
|
A | AT | 7 | a0001c0002t0001g0019a0001c0003t0003g0231a0002c0001t0001g0066others(4): Show | 10 | HG02074.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1613+1657dupT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 30624109 | |||||
chr7:30624164
|
G | T | 13 | a0002c0001t0001g0025a0002c0001t0001g0026a0002c0001t0001g0027others(10): Show | 16 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1613+1702G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30624164 | ||||||
chr7:30624382
|
T | G | 3 | a0001c0004t0002g0051a0001c0004t0002g0052a0001c0004t0002g0053 | 3 | HG01081.hp2 HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1614-1852T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30624382 | ||||||
chr7:30624559
|
A | G | 57 | a0001c0003t0003g0006a0001c0003t0003g0012a0001c0003t0003g0013others(54): Show | 80 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.1614-1675A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30624559 | ||||||
chr7:30624609
|
C | G | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1614-1625C>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30624609 | ||||||
chr7:30624673
|
A | C | 1 | a0001c0003t0003g0244 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1614-1561A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30624673 | ||||||
chr7:30624713
|
A | G | 1 | a0001c0002t0002g0172 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1614-1521A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30624713 | ||||||
chr7:30624772
|
C | T | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1614-1462C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30624772 | ||||||
chr7:30624798
|
C | T | 6 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(3): Show | 8 | HG01891.hp2 HG01978.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1614-1436C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30624798 | ||||||
chr7:30624950
|
C | CT | 7 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(4): Show | 9 | HG00408.hp1 HG01891.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1614-1274dupT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr7 | 30624950 | |||||
chr7:30625062
|
C | T | 5 | a0002c0001t0001g0018a0002c0001t0001g0077a0002c0001t0001g0080others(2): Show | 7 | HG02257.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1614-1172C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625062 | ||||||
chr7:30625100
|
G | A | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1614-1134G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625100 | ||||||
chr7:30625133
|
G | A | 1 | a0001c0003t0003g0239 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1614-1101G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625133 | ||||||
chr7:30625263
|
G | A | 80 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(77): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1614-971G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625263 | ||||||
chr7:30625271
|
C | T | 1 | a0001c0003t0003g0039 | 2 | HG00609.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.1614-963C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625271 | ||||||
chr7:30625344
|
T | G | 2 | a0001c0002t0002g0142a0001c0002t0002g0162 | 2 | NA18970.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1614-890T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625344 | ||||||
chr7:30625366
|
A | T | 80 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(77): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1614-868A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625366 | ||||||
chr7:30625425
|
G | A | 14 | a0001c0002t0004g0042a0001c0004t0002g0005a0001c0004t0002g0049others(11): Show | 25 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1614-809G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625425 | ||||||
chr7:30625644
|
A | G | 2 | a0002c0001t0001g0061a0002c0001t0001g0065 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1614-590A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625644 | ||||||
chr7:30625735
|
A | C | 6 | a0001c0003t0003g0038a0001c0003t0003g0220a0001c0003t0003g0221others(3): Show | 7 | HG01123.hp1 HG01167.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1614-499A>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625735 | ||||||
chr7:30625816
|
T | C | 2 | a0001c0004t0002g0049a0001c0004t0002g0050 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1614-418T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625816 | ||||||
chr7:30625963
|
A | G | 2 | a0002c0001t0001g0020a0002c0001t0001g0131 | 4 | HG00741.hp1 HG02698.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614-271A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 12/16 | chr7 | 30625963 | ||||||
chr7:30626439
|
C | T | 2 | a0001c0003t0003g0222a0001c0003t0003g0224 | 2 | NA18956.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1699+120C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30626439 | ||||||
chr7:30626474
|
G | A | 1 | a0002c0001t0001g0102 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1699+155G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30626474 | ||||||
chr7:30626559
|
C | T | 1 | a0003c0006t0001g0079 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1699+240C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30626559 | ||||||
chr7:30626604
|
G | A | 15 | a0001c0002t0004g0042a0001c0004t0002g0005a0001c0004t0002g0049others(12): Show | 26 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1699+285G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30626604 | ||||||
chr7:30626800
|
G | A | 1 | a0001c0002t0002g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1699+481G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30626800 | ||||||
chr7:30626810
|
G | A | 2 | a0001c0002t0002g0143a0001c0002t0002g0163 | 2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1699+491G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30626810 | ||||||
chr7:30626851
|
C | T | 11 | a0001c0002t0002g0009a0001c0002t0002g0135a0001c0002t0002g0142others(8): Show | 15 | HG00597.hp2 HG01192.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.1699+532C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30626851 | ||||||
chr7:30626938
|
G | T | 1 | a0002c0001t0001g0118 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1699+619G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30626938 | ||||||
chr7:30626960
|
G | A | 1 | a0002c0001t0001g0129 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1699+641G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30626960 | ||||||
chr7:30626980
|
C | CA | 11 | a0001c0002t0002g0136a0001c0002t0002g0158a0001c0002t0002g0164others(8): Show | 20 | HG01109.hp1 HG01256.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.1699+677dupA | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 30626980 | |||||
chr7:30626980
|
CA | C | 9 | a0001c0002t0002g0088a0001c0003t0003g0203a0001c0005t0002g0016others(6): Show | 11 | HG01168.hp1 HG01891.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1699+677delA | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 30626980 | |||||
chr7:30627014
|
T | G | 2 | a0001c0004t0002g0052a0001c0004t0002g0053 | 2 | HG01081.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1699+695T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30627014 | ||||||
chr7:30627022
|
G | A | 1 | a0001c0013t0002g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1699+703G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30627022 | ||||||
chr7:30627029
|
T | G | 1 | a0001c0013t0002g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1699+710T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30627029 | ||||||
chr7:30627045
|
G | A | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1699+726G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30627045 | ||||||
chr7:30627323
|
A | T | 3 | a0001c0002t0002g0145a0001c0002t0002g0146a0001c0002t0002g0167 | 3 | NA18988.hp1 NA19006.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1699+1004A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30627323 | ||||||
chr7:30627817
|
A | G | 226 | a0001c0002t0001g0019a0001c0002t0002g0001a0001c0002t0002g0009others(223): Show | 354 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.1700-743A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30627817 | ||||||
chr7:30627956
|
C | T | 1 | a0001c0002t0002g0149 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1700-604C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30627956 | ||||||
chr7:30628057
|
C | T | 4 | a0001c0007t0001g0024a0001c0007t0001g0056a0001c0007t0001g0057others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1700-503C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30628057 | ||||||
chr7:30628199
|
T | C | 1 | a0001c0003t0003g0246 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1700-361T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30628199 | ||||||
chr7:30628243
|
G | A | 1 | a0001c0002t0002g0165 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1700-317G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30628243 | ||||||
chr7:30628433
|
C | T | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1700-127C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30628433 | ||||||
chr7:30628475
|
G | A | 1 | a0001c0005t0002g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1700-85G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30628475 | ||||||
chr7:30628515
|
T | C | 1 | a0001c0002t0002g0022 | 3 | HG01516.hp2 HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1700-45T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 13/16 | chr7 | 30628515 | ||||||
chr7:30628913
|
T | G | 1 | a0001c0002t0002g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1809+244T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30628913 | ||||||
chr7:30629184
|
G | T | 1 | a0002c0001t0001g0017 | 3 | HG02486.hp1 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1809+515G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629184 | ||||||
chr7:30629192
|
A | T | 1 | a0001c0004t0002g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1809+523A>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629192 | ||||||
chr7:30629233
|
G | C | 1 | a0001c0002t0004g0042 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1809+564G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629233 | ||||||
chr7:30629266
|
G | A | 80 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(77): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1809+597G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629266 | ||||||
chr7:30629345
|
T | C | 2 | a0001c0004t0002g0049a0001c0004t0002g0050 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1809+676T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629345 | ||||||
chr7:30629375
|
C | G | 1 | a0001c0003t0003g0241 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1809+706C>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629375 | ||||||
chr7:30629541
|
CT | C | 6 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(3): Show | 8 | HG01891.hp2 HG01978.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1809+874delT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 30629541 | |||||
chr7:30629638
|
C | T | 2 | a0002c0001t0001g0061a0002c0001t0001g0065 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1809+969C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629638 | ||||||
chr7:30629792
|
G | C | 1 | a0002c0001t0001g0126 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1809+1123G>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629792 | ||||||
chr7:30629821
|
G | T | 3 | a0001c0002t0002g0145a0001c0002t0002g0146a0001c0002t0002g0167 | 3 | NA18988.hp1 NA19006.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1809+1152G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629821 | ||||||
chr7:30629888
|
G | T | 1 | a0001c0002t0002g0166 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1809+1219G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629888 | ||||||
chr7:30629889
|
C | T | 1 | a0001c0002t0002g0166 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1809+1220C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629889 | ||||||
chr7:30629903
|
A | G | 1 | a0002c0001t0001g0110 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1809+1234A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30629903 | ||||||
chr7:30630183
|
G | T | 2 | a0001c0002t0002g0034a0001c0002t0002g0154 | 3 | NA18943.hp2 NA19066.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1810-1265G>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30630183 | ||||||
chr7:30630190
|
G | A | 14 | a0001c0002t0004g0042a0001c0004t0002g0005a0001c0004t0002g0049others(11): Show | 25 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1810-1258G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30630190 | ||||||
chr7:30630202
|
T | C | 7 | a0001c0004t0002g0005a0001c0004t0002g0049a0001c0004t0002g0050others(4): Show | 16 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1810-1246T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30630202 | ||||||
chr7:30630517
|
C | CT | 21 | a0001c0002t0002g0036a0001c0002t0002g0146a0001c0002t0002g0163others(18): Show | 23 | HG00544.hp1 HG01346.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1810-912dupT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 30630517 | |||||
chr7:30630517
|
CT | C | 25 | a0001c0003t0003g0006a0001c0003t0003g0037a0001c0003t0003g0039others(22): Show | 39 | HG00609.hp1 HG00673.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1810-912delT | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 30630517 | |||||
chr7:30630543
|
G | A | 1 | a0002c0001t0001g0060 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1810-905G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30630543 | ||||||
chr7:30630717
|
C | A | 4 | a0002c0001t0001g0031a0002c0001t0001g0109a0002c0001t0001g0111others(1): Show | 5 | HG01175.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1810-731C>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30630717 | ||||||
chr7:30630908
|
T | C | 1 | a0001c0002t0002g0168 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1810-540T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30630908 | ||||||
chr7:30631298
|
T | C | 1 | a0001c0003t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1810-150T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30631298 | ||||||
chr7:30631340
|
G | A | 1 | a0002c0001t0001g0063 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1810-108G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30631340 | ||||||
chr7:30631341
|
T | G | 1 | a0001c0013t0002g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1810-107T>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 14/16 | chr7 | 30631341 | ||||||
chr7:30631925
|
C | T | 15 | a0001c0002t0004g0042a0001c0004t0002g0005a0001c0004t0002g0049others(12): Show | 26 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1904-322C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 15/16 | chr7 | 30631925 | ||||||
chr7:30632003
|
C | T | 1 | a0001c0002t0002g0146 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1904-244C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 15/16 | chr7 | 30632003 | ||||||
chr7:30632566
|
G | A | 1 | a0001c0004t0002g0005 | 10 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2094+129G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/16 | chr7 | 30632566 | ||||||
chr7:30632646
|
A | G | 1 | a0002c0001t0001g0111 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2094+209A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/16 | chr7 | 30632646 | ||||||
chr7:30632713
|
A | AC | 3 | a0002c0001t0001g0008a0002c0001t0001g0082a0002c0001t0001g0092 | 8 | HG01109.hp2 HG02145.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+276_2094+277i others(3): Show |
GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/16 | chr7 | 30632713 | ||||||
chr7:30632714
|
G | A | 3 | a0002c0001t0001g0008a0002c0001t0001g0082a0002c0001t0001g0092 | 8 | HG01109.hp2 HG02145.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2094+277G>A | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/16 | chr7 | 30632714 | ||||||
chr7:30632748
|
T | C | 1 | a0002c0001t0001g0115 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2094+311T>C | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/16 | chr7 | 30632748 | ||||||
chr7:30633028
|
A | G | 1 | a0001c0002t0002g0169 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2094+591A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/16 | chr7 | 30633028 | ||||||
chr7:30633135
|
A | G | 57 | a0001c0003t0003g0006a0001c0003t0003g0012a0001c0003t0003g0013others(54): Show | 80 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.2095-600A>G | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/16 | chr7 | 30633135 | ||||||
chr7:30633245
|
C | T | 6 | a0001c0005t0002g0016a0001c0005t0002g0045a0001c0005t0002g0046others(3): Show | 8 | HG01891.hp2 HG01978.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2095-490C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/16 | chr7 | 30633245 | ||||||
chr7:30633307
|
C | T | 15 | a0001c0002t0004g0042a0001c0004t0002g0005a0001c0004t0002g0049others(12): Show | 26 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.2095-428C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/16 | chr7 | 30633307 | ||||||
chr7:30633729
|
C | T | 81 | a0001c0002t0002g0001a0001c0002t0002g0009a0001c0002t0002g0011others(78): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
splice_region_variant&intron_variant | LOW | c.2095-6C>T | GARS1 | ENSG00000106105.15 | transcript | ENST00000389266.8 | protein_coding | 16/16 | chr7 | 30633729 |