| geneid | 10352 |
|---|---|
| ensemblid | ENSG00000116874.12 |
| hgncid | 12730 |
| symbol | WARS2 |
| name | tryptophanyl tRNA synthetase 2, mitochondrial |
| refseq_nuc | NM_015836.4 |
| refseq_prot | NP_056651.1 |
| ensembl_nuc | ENST00000235521.5 |
| ensembl_prot | ENSP00000235521.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 119031216 |
| end | 119140653 |
| strand | - |
| ver | v1.2 |
| region | chr1:119031216-119140653 |
| region5000 | chr1:119026216-119145653 |
| regionname0 | WARS2_chr1_119031216_119140653 |
| regionname5000 | WARS2_chr1_119026216_119145653 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 360 | 282 | 70 | 56 | 118 | 6 | 31 | 90 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0002 | 0/1 | 360 | 64 | 15 | 4 | 42 | 1 | 1 | 32 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0003 | 0/0 | 360 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0004 | 0/0 | 360 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0005 | 0/0 | 360 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0006 | 0/0 | 360 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| 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 | 1083 | 260 | 61 | 52 | 117 | 6 | 23 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| c0002 | 0/1 | 1083 | 64 | 15 | 4 | 42 | 1 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| c0003 | 0/0 | 1083 | 18 | 6 | 4 | 1 | 0 | 7 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| c0004 | 0/0 | 1083 | 4 | 4 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| c0005 | 0/0 | 1083 | 2 | 1 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| c0006 | 0/0 | 1083 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| c0007 | 0/0 | 1083 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| c0008 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| c0009 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| c0010 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1705 | 86 | 3 | 19 | 60 | 2 | 2 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0002 | 0/1 | 1705 | 62 | 13 | 4 | 42 | 1 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0003 | 1/0 | 1705 | 59 | 8 | 12 | 25 | 2 | 11 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0004 | 0/0 | 1705 | 41 | 23 | 1 | 12 | 0 | 5 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0005 | 0/0 | 1705 | 30 | 10 | 8 | 12 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0006 | 0/0 | 1705 | 27 | 7 | 10 | 4 | 1 | 5 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0007 | 0/0 | 1705 | 23 | 2 | 6 | 6 | 2 | 7 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0008 | 0/0 | 1705 | 10 | 10 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0009 | 0/0 | 1705 | 5 | 5 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0010 | 0/0 | 1705 | 4 | 4 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0011 | 0/0 | 1705 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0012 | 0/0 | 1705 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0013 | 0/0 | 1705 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0014 | 0/0 | 1705 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0015 | 0/0 | 1705 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| t0016 | 0/0 | 1705 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1083 | 260 | 61 | 52 | 117 | 6 | 23 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0003 | 0/0 | 1083 | 18 | 6 | 4 | 1 | 0 | 7 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0006 | 0/0 | 1083 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0007 | 0/0 | 1083 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0010 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0002c0002 | 0/1 | 1083 | 64 | 15 | 4 | 42 | 1 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0003c0004 | 0/0 | 1083 | 4 | 4 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0004c0005 | 0/0 | 1083 | 2 | 1 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0005c0008 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0006c0009 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2787 | 83 | 2 | 19 | 59 | 1 | 2 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0003 | 1/0 | 2787 | 58 | 8 | 12 | 24 | 2 | 11 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0004 | 0/0 | 2787 | 37 | 20 | 1 | 12 | 0 | 4 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0005 | 0/0 | 2787 | 26 | 6 | 8 | 12 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0006 | 0/0 | 2787 | 27 | 7 | 10 | 4 | 1 | 5 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0007 | 0/0 | 2787 | 10 | 1 | 2 | 5 | 2 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0008 | 0/0 | 2787 | 10 | 10 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0010 | 0/0 | 2787 | 4 | 4 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0012 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0013 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0014 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0015 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0001t0016 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0003t0007 | 0/0 | 2787 | 13 | 1 | 4 | 1 | 0 | 7 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0003t0009 | 0/0 | 2787 | 5 | 5 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0006t0004 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0007t0004 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0001c0010t0004 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0002c0002t0002 | 0/1 | 2787 | 62 | 13 | 4 | 42 | 1 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0002c0002t0011 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0003c0004t0005 | 0/0 | 2787 | 4 | 4 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0004c0005t0001 | 0/0 | 2787 | 2 | 1 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0005c0008t0001 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| a0006c0009t0003 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | copy fasta | chr1 | 119026216 | 119145653 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0006g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0007g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0010g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0010g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0010g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0013g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0014g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0015g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0001t0016g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0007g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0009g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0003t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0006t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0006t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0007t0004g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0001c0010t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0001 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0002c0002t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0003c0004t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0003c0004t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0003c0004t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0003c0004t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0004c0005t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0004c0005t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0005c0008t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| a0006c0009t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0055 | EUR | GBR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0265 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0205 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0206 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0273 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0207 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0311 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG00741 | hp2 | a0001 | c0003 | t0007 | g0221 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0163 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0331 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01099 | hp2 | a0001 | c0003 | t0007 | g0222 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0202 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0315 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0148 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01168 | hp1 | a0001 | c0003 | t0007 | g0218 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0322 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0321 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0133 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0138 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0314 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0164 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0155 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0204 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0150 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | IBS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0271 | EUR | IBS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0237 | EUR | IBS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0208 | EUR | IBS | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0318 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01978 | hp1 | a0001 | c0003 | t0007 | g0219 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0151 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0137 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0135 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0159 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0278 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | CDX | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CDX | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02165 | hp1 | a0001 | c0003 | t0007 | g0297 | EAS | CDX | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | CDX | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0325 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02258 | hp2 | a0001 | c0003 | t0009 | g0226 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02280 | hp1 | a0001 | c0006 | t0004 | g0025 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02280 | hp2 | a0002 | c0002 | t0011 | g0129 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0334 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0283 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02572 | hp2 | a0001 | c0003 | t0009 | g0021 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0319 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02602 | hp2 | a0001 | c0001 | t0014 | g0063 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0338 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02622 | hp2 | a0002 | c0002 | t0011 | g0130 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0139 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0214 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02647 | hp1 | a0003 | c0004 | t0005 | g0213 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02647 | hp2 | a0001 | c0010 | t0004 | g0287 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02683 | hp1 | a0001 | c0003 | t0007 | g0220 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0327 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0286 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02723 | hp2 | a0003 | c0004 | t0005 | g0307 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02735 | hp2 | a0001 | c0003 | t0007 | g0295 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0329 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0303 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0281 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02896 | hp2 | a0001 | c0003 | t0009 | g0223 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02897 | hp1 | a0001 | c0003 | t0009 | g0225 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0125 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02970 | hp2 | a0003 | c0004 | t0005 | g0211 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02976 | hp1 | a0001 | c0001 | t0015 | g0275 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0153 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0301 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0320 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0276 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03130 | hp2 | a0001 | c0006 | t0004 | g0175 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0337 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0285 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0282 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0136 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03239 | hp1 | a0001 | c0003 | t0007 | g0298 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0292 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0340 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0339 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03490 | hp2 | a0001 | c0003 | t0007 | g0227 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0269 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0152 | AFR | ESN | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0142 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0304 | AFR | GWD | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0309 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03704 | hp2 | a0001 | c0003 | t0007 | g0228 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03710 | hp1 | a0001 | c0003 | t0007 | g0296 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0242 | SAS | PJL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0312 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0267 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0246 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0110 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0308 | SAS | BEB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04115 | hp2 | a0001 | c0007 | t0004 | g0014 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0330 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04204 | hp2 | a0001 | c0003 | t0007 | g0289 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0274 | SAS | STU | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0280 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0332 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0333 | EAS | CHB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | CHB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18906 | hp1 | a0003 | c0004 | t0005 | g0212 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0277 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0201 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18941 | hp1 | a0001 | c0001 | t0007 | g0203 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0162 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0160 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18968 | hp2 | a0006 | c0009 | t0003 | g0326 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18981 | hp1 | a0005 | c0008 | t0001 | g0109 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19004 | hp2 | a0001 | c0001 | t0013 | g0084 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0169 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0144 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0335 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0288 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0266 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0154 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0143 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0300 | AFR | YRI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | ASW | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20129 | hp2 | a0001 | c0003 | t0007 | g0254 | AFR | ASW | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0310 | EUR | TSI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20752 | hp2 | a0004 | c0005 | t0001 | g0015 | EUR | TSI | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0317 | SAS | GIH | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0236 | SAS | GIH | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0316 | AMR | CLM | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0293 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0336 | AFR | ACB | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0132 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | MSL | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG06807 | hp1 | a0001 | c0003 | t0009 | g0224 | AFR | USA | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0328 | AFR | USA | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0016 | AFR | USA | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | USA | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | LWK | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0118 | REF | REF | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0027 | REF | REF | WARS2_chr1_119026216_119145653 | WARS2 | chr1 | 119026216 | 119145653 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119032915
|
A | G | 1 | a0003 | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
missense_variant | MODERATE | c.1079T>C | p.Leu360Pro | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1088/2787 | 1079/1083 | 360/360 | chr1 | 119032915 | ||
| chr1:119033045
|
T | C | 1 | a0006 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.949A>G | p.Ile317Val | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 958/2787 | 949/1083 | 317/360 | chr1 | 119033045 | ||
| chr1:119033135
|
C | T | 1 | a0005 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.859G>A | p.Val287Met | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 868/2787 | 859/1083 | 287/360 | chr1 | 119033135 | ||
| chr1:119033195
|
C | G | 1 | a0002 | 64 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(61): Show |
missense_variant | MODERATE | c.799G>C | p.Ala267Pro | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 808/2787 | 799/1083 | 267/360 | chr1 | 119033195 | ||
| chr1:119140608
|
A | C | 1 | a0004 | 2 | NA20300.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.37T>G | p.Trp13Gly | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/6 | 46/2787 | 37/1083 | 13/360 | chr1 | 119140608 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119033358
|
T | C | 1 | a0001c0010 | 1 | HG02647.hp2 | splice_region_variant&synonymous_variant | LOW | c.636A>G | p.Thr212Thr | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 645/2787 | 636/1083 | 212/360 | chr1 | 119033358 | ||
| chr1:119042326
|
G | A | 1 | a0001c0003 | 18 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(15): Show |
synonymous_variant | LOW | c.453C>T | p.His151His | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/6 | 462/2787 | 453/1083 | 151/360 | chr1 | 119042326 | ||
| chr1:119076551
|
C | G | 1 | a0001c0006 | 2 | HG02280.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.147G>C | p.Leu49Leu | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/6 | 156/2787 | 147/1083 | 49/360 | chr1 | 119076551 | ||
| chr1:119140618
|
C | G | 1 | a0001c0007 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.27G>C | p.Ala9Ala | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/6 | 36/2787 | 27/1083 | 9/360 | chr1 | 119140618 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119031219
|
G | C | 1 | a0001c0001t0015 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1692C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1692 | chr1 | 119031219 | |||||
| chr1:119031233
|
C | T | 1 | a0001c0001t0016 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1678G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1678 | chr1 | 119031233 | |||||
| chr1:119031237
|
T | C | 1 | a0001c0001t0006 | 27 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1674A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1674 | chr1 | 119031237 | |||||
| chr1:119031451
|
G | C | 22 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(19): Show | 295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*1460C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1460 | chr1 | 119031451 | |||||
| chr1:119031659
|
A | T | 1 | a0001c0001t0010 | 4 | HG02818.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1252T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1252 | chr1 | 119031659 | |||||
| chr1:119031666
|
G | A | 5 | a0001c0001t0001a0001c0001t0013a0001c0001t0014others(2): Show | 88 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1245C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1245 | chr1 | 119031666 | |||||
| chr1:119031759
|
A | G | 1 | a0002c0002t0011 | 2 | HG02280.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1152T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1152 | chr1 | 119031759 | |||||
| chr1:119031806
|
A | G | 1 | a0001c0001t0014 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1105T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1105 | chr1 | 119031806 | |||||
| chr1:119031830
|
C | T | 2 | a0001c0001t0008a0001c0001t0015 | 11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1081G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1081 | chr1 | 119031830 | |||||
| chr1:119031884
|
C | G | 1 | a0001c0001t0013 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1027G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 1027 | chr1 | 119031884 | |||||
| chr1:119031914
|
G | A | 5 | a0001c0001t0001a0001c0001t0013a0001c0001t0014others(2): Show | 88 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*997C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 997 | chr1 | 119031914 | |||||
| chr1:119031964
|
C | T | 15 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(12): Show | 192 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*947G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 947 | chr1 | 119031964 | |||||
| chr1:119032098
|
G | T | 1 | a0001c0001t0016 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*813C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 813 | chr1 | 119032098 | |||||
| chr1:119032108
|
G | A | 1 | a0001c0003t0009 | 5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*803C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 803 | chr1 | 119032108 | |||||
| chr1:119032308
|
C | T | 1 | a0001c0001t0012 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 603 | chr1 | 119032308 | |||||
| chr1:119032342
|
G | A | 2 | a0001c0001t0008a0001c0001t0015 | 11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*569C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 569 | chr1 | 119032342 | |||||
| chr1:119032547
|
C | A | 7 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(4): Show | 73 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*364G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 364 | chr1 | 119032547 | |||||
| chr1:119032609
|
T | C | 7 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(4): Show | 73 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*302A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 302 | chr1 | 119032609 | |||||
| chr1:119032674
|
C | G | 2 | a0002c0002t0002a0002c0002t0011 | 64 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*237G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 6/6 | 237 | chr1 | 119032674 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:119033552
|
C | T | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.635-193G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 5/5 | chr1 | 119033552 | ||||||
| chr1:119033834
|
T | A | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.634+261A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 5/5 | chr1 | 119033834 | ||||||
| chr1:119033839
|
T | A | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.634+256A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 5/5 | chr1 | 119033839 | ||||||
| chr1:119033967
|
A | G | 2 | a0001c0001t0006g0321a0001c0001t0006g0322 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.634+128T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 5/5 | chr1 | 119033967 | ||||||
| chr1:119034281
|
G | A | 11 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(8): Show | 11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-68C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034281 | ||||||
| chr1:119034579
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(90): Show | 95 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.516-366G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034579 | ||||||
| chr1:119034611
|
T | C | 4 | a0001c0001t0010g0292a0001c0001t0010g0300a0001c0001t0010g0303others(1): Show | 4 | HG02818.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.516-398A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034611 | ||||||
| chr1:119034631
|
C | G | 1 | a0001c0001t0006g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.516-418G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034631 | ||||||
| chr1:119034693
|
T | C | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.516-480A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034693 | ||||||
| chr1:119034787
|
T | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(270): Show | 284 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.516-574A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034787 | ||||||
| chr1:119034869
|
C | T | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.516-656G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119034869 | ||||||
| chr1:119035043
|
G | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(157): Show | 165 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.516-830C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035043 | ||||||
| chr1:119035114
|
T | G | 1 | a0003c0004t0005g0307 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.516-901A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035114 | ||||||
| chr1:119035214
|
A | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(157): Show | 165 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.516-1001T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035214 | ||||||
| chr1:119035294
|
A | T | 1 | a0002c0002t0002g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.516-1081T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035294 | ||||||
| chr1:119035302
|
G | A | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.516-1089C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035302 | ||||||
| chr1:119035324
|
C | G | 27 | a0001c0001t0007g0055a0001c0001t0007g0201a0001c0001t0007g0203others(24): Show | 27 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.516-1111G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035324 | ||||||
| chr1:119035427
|
C | T | 1 | a0001c0003t0009g0021 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.516-1214G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035427 | ||||||
| chr1:119035437
|
C | T | 1 | a0002c0002t0002g0180 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.516-1224G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035437 | ||||||
| chr1:119035695
|
A | G | 58 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(55): Show | 64 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.516-1482T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035695 | ||||||
| chr1:119035789
|
T | C | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.516-1576A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035789 | ||||||
| chr1:119035856
|
A | C | 1 | a0001c0007t0004g0014 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.516-1643T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119035856 | ||||||
| chr1:119036039
|
T | C | 2 | a0002c0002t0002g0122a0002c0002t0002g0126 | 2 | HG02129.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.516-1826A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036039 | ||||||
| chr1:119036054
|
A | G | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.516-1841T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036054 | ||||||
| chr1:119036097
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(87): Show | 92 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.516-1884G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036097 | ||||||
| chr1:119036104
|
T | C | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.516-1891A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036104 | ||||||
| chr1:119036134
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.516-1921G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036134 | ||||||
| chr1:119036208
|
G | GAAAAAT | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(86): Show | 91 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.516-2001_516-1996d others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036208 | ||||||
| chr1:119036306
|
G | A | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.516-2093C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036306 | ||||||
| chr1:119036456
|
C | T | 20 | a0001c0001t0007g0055a0001c0001t0007g0201a0001c0001t0007g0203others(17): Show | 20 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.516-2243G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036456 | ||||||
| chr1:119036653
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0031others(52): Show | 56 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.516-2440T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036653 | ||||||
| chr1:119036689
|
C | T | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.516-2476G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036689 | ||||||
| chr1:119036771
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.516-2558T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119036771 | ||||||
| chr1:119037113
|
C | A | 2 | a0002c0002t0002g0125a0002c0002t0002g0133 | 2 | HG01175.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.516-2900G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037113 | ||||||
| chr1:119037322
|
AC | A | 65 | a0001c0001t0003g0268a0001c0001t0004g0011a0001c0001t0004g0012others(62): Show | 68 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.516-3110delG | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037322 | ||||||
| chr1:119037363
|
G | A | 11 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(8): Show | 11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-3150C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037363 | ||||||
| chr1:119037629
|
T | C | 51 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(48): Show | 57 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.516-3416A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037629 | ||||||
| chr1:119037689
|
C | T | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.516-3476G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037689 | ||||||
| chr1:119037720
|
C | A | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.516-3507G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037720 | ||||||
| chr1:119037923
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.516-3710T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119037923 | ||||||
| chr1:119038140
|
A | T | 1 | a0001c0001t0003g0238 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.516-3927T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038140 | ||||||
| chr1:119038169
|
G | A | 11 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(8): Show | 11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-3956C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038169 | ||||||
| chr1:119038186
|
G | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.516-3973C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038186 | ||||||
| chr1:119038218
|
G | T | 10 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-4005C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038218 | ||||||
| chr1:119038378
|
G | A | 1 | a0002c0002t0002g0128 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.515+3886C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038378 | ||||||
| chr1:119038422
|
A | G | 1 | a0002c0002t0002g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.515+3842T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038422 | ||||||
| chr1:119038528
|
T | C | 22 | a0001c0001t0005g0117a0001c0001t0005g0123a0001c0001t0005g0131others(19): Show | 22 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.515+3736A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038528 | ||||||
| chr1:119038717
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.515+3547C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038717 | ||||||
| chr1:119038760
|
G | A | 1 | a0002c0002t0002g0181 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.515+3504C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038760 | ||||||
| chr1:119038781
|
G | A | 71 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(68): Show | 74 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.515+3483C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038781 | ||||||
| chr1:119038935
|
G | A | 5 | a0001c0003t0009g0021a0001c0003t0009g0223a0001c0003t0009g0224others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.515+3329C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038935 | ||||||
| chr1:119038977
|
C | T | 1 | a0003c0004t0005g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.515+3287G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038977 | ||||||
| chr1:119038987
|
C | T | 59 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(56): Show | 65 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.515+3277G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119038987 | ||||||
| chr1:119039277
|
C | T | 67 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(64): Show | 70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.515+2987G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039277 | ||||||
| chr1:119039314
|
T | C | 59 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(56): Show | 65 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.515+2950A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039314 | ||||||
| chr1:119039501
|
A | G | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+2763T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039501 | ||||||
| chr1:119039625
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.515+2639A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039625 | ||||||
| chr1:119039695
|
C | G | 1 | a0001c0001t0007g0206 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.515+2569G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039695 | ||||||
| chr1:119039714
|
T | G | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.515+2550A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039714 | ||||||
| chr1:119039768
|
C | G | 18 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(15): Show | 18 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.515+2496G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039768 | ||||||
| chr1:119039825
|
G | A | 67 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(64): Show | 70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.515+2439C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119039825 | ||||||
| chr1:119040019
|
C | T | 67 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(64): Show | 70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.515+2245G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040019 | ||||||
| chr1:119040089
|
C | T | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.515+2175G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040089 | ||||||
| chr1:119040198
|
A | C | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.515+2066T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040198 | ||||||
| chr1:119040321
|
C | T | 1 | a0001c0001t0003g0230 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.515+1943G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040321 | ||||||
| chr1:119040341
|
T | C | 1 | a0001c0001t0003g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.515+1923A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040341 | ||||||
| chr1:119040446
|
G | A | 5 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0301others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.515+1818C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040446 | ||||||
| chr1:119040513
|
C | G | 11 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(8): Show | 11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.515+1751G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040513 | ||||||
| chr1:119040558
|
C | T | 1 | a0001c0001t0007g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.515+1706G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040558 | ||||||
| chr1:119040799
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(94): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.515+1465T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040799 | ||||||
| chr1:119040945
|
A | T | 1 | a0001c0001t0004g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.515+1319T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119040945 | ||||||
| chr1:119041100
|
T | A | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.515+1164A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041100 | ||||||
| chr1:119041157
|
A | G | 4 | a0001c0001t0010g0292a0001c0001t0010g0300a0001c0001t0010g0303others(1): Show | 4 | HG02818.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.515+1107T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041157 | ||||||
| chr1:119041183
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.515+1081C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041183 | ||||||
| chr1:119041214
|
A | T | 77 | a0001c0001t0001g0141a0001c0003t0007g0218a0001c0003t0007g0219others(74): Show | 83 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.515+1050T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041214 | ||||||
| chr1:119041231
|
C | A | 99 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(96): Show | 102 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.515+1033G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041231 | ||||||
| chr1:119041303
|
C | T | 18 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(15): Show | 18 | HG00558.hp1 HG00609.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.515+961G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041303 | ||||||
| chr1:119041315
|
A | G | 1 | a0001c0001t0005g0166 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.515+949T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041315 | ||||||
| chr1:119041345
|
T | A | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(270): Show | 284 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.515+919A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041345 | ||||||
| chr1:119041704
|
T | C | 3 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213 | 3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.515+560A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041704 | ||||||
| chr1:119041773
|
G | A | 71 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(68): Show | 74 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.515+491C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041773 | ||||||
| chr1:119041868
|
T | C | 3 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0010t0004g0287 | 3 | HG01891.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.515+396A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119041868 | ||||||
| chr1:119042037
|
A | G | 59 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(56): Show | 65 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.515+227T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119042037 | ||||||
| chr1:119042102
|
C | A | 1 | a0001c0001t0004g0171 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.515+162G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119042102 | ||||||
| chr1:119042129
|
T | C | 1 | a0001c0007t0004g0014 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.515+135A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119042129 | ||||||
| chr1:119042156
|
C | T | 7 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(4): Show | 7 | HG00408.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+108G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 4/5 | chr1 | 119042156 | ||||||
| chr1:119042366
|
G | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-17C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042366 | ||||||
| chr1:119042527
|
A | G | 4 | a0002c0002t0002g0182a0002c0002t0002g0187a0002c0002t0002g0189others(1): Show | 4 | HG00423.hp2 NA18747.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-178T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042527 | ||||||
| chr1:119042692
|
G | A | 4 | a0001c0001t0006g0158a0001c0001t0006g0159a0001c0001t0006g0160others(1): Show | 4 | HG02056.hp2 HG02071.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-343C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042692 | ||||||
| chr1:119042848
|
T | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG00673.hp2 NA19003.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.430-499A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042848 | ||||||
| chr1:119042874
|
A | G | 67 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(64): Show | 70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.430-525T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042874 | ||||||
| chr1:119042875
|
G | A | 1 | a0001c0001t0003g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.430-526C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042875 | ||||||
| chr1:119042959
|
C | G | 5 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0301others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-610G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119042959 | ||||||
| chr1:119043119
|
C | T | 1 | a0003c0004t0005g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.430-770G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043119 | ||||||
| chr1:119043216
|
CTAAGGTA others(17): Show |
C | 1 | a0001c0001t0006g0309 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.430-891_430-868del others(24): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043216 | ||||||
| chr1:119043371
|
C | T | 5 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0301others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-1022G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043371 | ||||||
| chr1:119043454
|
C | T | 8 | a0002c0002t0002g0132a0002c0002t0002g0135a0002c0002t0002g0136others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-1105G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043454 | ||||||
| chr1:119043653
|
C | T | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.430-1304G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043653 | ||||||
| chr1:119043668
|
A | G | 1 | a0001c0001t0012g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.430-1319T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043668 | ||||||
| chr1:119043769
|
G | C | 16 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(13): Show | 16 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-1420C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119043769 | ||||||
| chr1:119044049
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.429+1533C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044049 | ||||||
| chr1:119044064
|
G | A | 64 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0022others(61): Show | 67 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.429+1518C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044064 | ||||||
| chr1:119044506
|
T | C | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.429+1076A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044506 | ||||||
| chr1:119044588
|
A | T | 1 | a0001c0001t0001g0085 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.429+994T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044588 | ||||||
| chr1:119044653
|
G | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+929C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044653 | ||||||
| chr1:119044683
|
T | G | 1 | a0001c0001t0005g0157 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.429+899A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044683 | ||||||
| chr1:119044705
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.429+877T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044705 | ||||||
| chr1:119044817
|
T | C | 67 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(64): Show | 70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.429+765A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044817 | ||||||
| chr1:119044857
|
A | G | 1 | a0001c0001t0004g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.429+725T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119044857 | ||||||
| chr1:119045014
|
G | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(10): Show | 13 | HG00558.hp1 HG00609.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+568C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119045014 | ||||||
| chr1:119045040
|
G | A | 1 | a0001c0001t0004g0317 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.429+542C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119045040 | ||||||
| chr1:119045060
|
G | A | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+522C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119045060 | ||||||
| chr1:119045427
|
C | T | 1 | a0001c0003t0007g0289 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.429+155G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 3/5 | chr1 | 119045427 | ||||||
| chr1:119045730
|
A | G | 16 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0179others(13): Show | 18 | HG00423.hp2 HG02015.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.349-68T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119045730 | ||||||
| chr1:119045937
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.349-275C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119045937 | ||||||
| chr1:119046005
|
A | ACT | 11 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(8): Show | 11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.349-345_349-344dup others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046005 | ||||||
| chr1:119046021
|
TCACACAC others(11): Show |
T | 1 | a0001c0001t0004g0171 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.349-377_349-360del others(18): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046021 | ||||||
| chr1:119046054
|
C | T | 4 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0251others(1): Show | 4 | HG00408.hp2 NA18948.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-392G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046054 | ||||||
| chr1:119046060
|
C | T | 1 | a0002c0002t0002g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349-398G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046060 | ||||||
| chr1:119046068
|
C | T | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.349-406G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046068 | ||||||
| chr1:119046152
|
G | A | 5 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0301others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-490C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046152 | ||||||
| chr1:119046285
|
GT | G | 41 | a0001c0001t0003g0008a0001c0001t0003g0069a0001c0001t0003g0093others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.349-624delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | ||||||
| chr1:119046285
|
GTT | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0040others(36): Show | 42 | HG00642.hp1 HG00673.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.349-625_349-624del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | ||||||
| chr1:119046285
|
GTTT | G | 72 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(69): Show | 73 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.349-626_349-624del others(3): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | ||||||
| chr1:119046285
|
GTTTT | G | 27 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0061others(24): Show | 29 | HG01167.hp1 HG01169.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.349-627_349-624del others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | ||||||
| chr1:119046285
|
GTTTTT | G | 38 | a0001c0001t0001g0141a0001c0003t0007g0218a0001c0003t0007g0219others(35): Show | 42 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.349-628_349-624del others(5): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | ||||||
| chr1:119046285
|
GTTTTTT | G | 46 | a0001c0001t0005g0117a0001c0001t0005g0123a0001c0001t0005g0131others(43): Show | 46 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.349-629_349-624del others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | ||||||
| chr1:119046285
|
GTTTTTTT | G | 70 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(67): Show | 73 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.349-630_349-624del others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046285 | ||||||
| chr1:119046508
|
C | T | 1 | a0001c0001t0003g0302 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.349-846G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046508 | ||||||
| chr1:119046514
|
A | AT | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(94): Show | 99 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.349-853dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046514 | ||||||
| chr1:119046514
|
AT | A | 80 | a0001c0001t0003g0069a0001c0001t0003g0271a0001c0001t0004g0011others(77): Show | 83 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.349-853delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046514 | ||||||
| chr1:119046614
|
C | T | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-952G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046614 | ||||||
| chr1:119046660
|
ATTTG | A | 7 | a0002c0002t0002g0195a0002c0002t0002g0197a0002c0002t0002g0198others(4): Show | 7 | HG02027.hp2 NA18950.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-1002_349-999de others(5): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046660 | ||||||
| chr1:119046720
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.349-1058G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046720 | ||||||
| chr1:119046774
|
C | CT | 22 | a0001c0001t0005g0117a0001c0001t0005g0123a0001c0001t0005g0131others(19): Show | 22 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.349-1113dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046774 | ||||||
| chr1:119046774
|
CT | C | 76 | a0001c0001t0001g0043a0001c0001t0001g0067a0001c0001t0001g0073others(73): Show | 79 | HG00408.hp1 HG00609.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.349-1113delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046774 | ||||||
| chr1:119046840
|
T | G | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.349-1178A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046840 | ||||||
| chr1:119046938
|
G | C | 1 | a0001c0003t0007g0220 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.349-1276C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119046938 | ||||||
| chr1:119047096
|
A | G | 1 | a0001c0001t0007g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.349-1434T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047096 | ||||||
| chr1:119047207
|
A | G | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG00558.hp1 NA18981.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-1545T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047207 | ||||||
| chr1:119047283
|
AT | A | 286 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(283): Show | 297 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.349-1622delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047283 | ||||||
| chr1:119047409
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0070 | 2 | NA19057.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.349-1747G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047409 | ||||||
| chr1:119047775
|
A | C | 79 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(76): Show | 82 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.349-2113T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047775 | ||||||
| chr1:119047797
|
C | T | 67 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(64): Show | 70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.349-2135G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047797 | ||||||
| chr1:119047842
|
T | C | 1 | a0001c0001t0006g0331 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.349-2180A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119047842 | ||||||
| chr1:119048021
|
T | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-2359A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048021 | ||||||
| chr1:119048140
|
A | G | 1 | a0001c0001t0015g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.349-2478T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048140 | ||||||
| chr1:119048238
|
G | A | 3 | a0001c0001t0005g0149a0001c0001t0005g0150a0001c0001t0005g0155 | 3 | HG01358.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.349-2576C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048238 | ||||||
| chr1:119048423
|
C | T | 74 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(71): Show | 77 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.349-2761G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048423 | ||||||
| chr1:119048562
|
A | G | 1 | a0002c0002t0002g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.349-2900T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048562 | ||||||
| chr1:119048794
|
G | C | 1 | a0001c0001t0004g0339 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.349-3132C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048794 | ||||||
| chr1:119048812
|
T | TCC | 70 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(67): Show | 73 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.349-3151_349-3150i others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048812 | ||||||
| chr1:119048881
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.349-3219A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048881 | ||||||
| chr1:119048923
|
T | C | 74 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(71): Show | 77 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.349-3261A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119048923 | ||||||
| chr1:119049196
|
C | A | 5 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0301others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-3534G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049196 | ||||||
| chr1:119049198
|
A | G | 7 | a0002c0002t0002g0180a0002c0002t0002g0182a0002c0002t0002g0186others(4): Show | 7 | HG00423.hp2 HG02040.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-3536T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049198 | ||||||
| chr1:119049317
|
C | A | 1 | a0001c0001t0006g0310 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.349-3655G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049317 | ||||||
| chr1:119049542
|
C | G | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(10): Show | 13 | HG00558.hp1 HG00609.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-3880G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049542 | ||||||
| chr1:119049564
|
T | C | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | NA18944.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.349-3902A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049564 | ||||||
| chr1:119049612
|
A | G | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.349-3950T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049612 | ||||||
| chr1:119049651
|
C | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-3989G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049651 | ||||||
| chr1:119049706
|
C | G | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.349-4044G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049706 | ||||||
| chr1:119049759
|
G | A | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-4097C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119049759 | ||||||
| chr1:119050048
|
A | C | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.349-4386T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050048 | ||||||
| chr1:119050150
|
C | G | 2 | a0001c0001t0003g0262a0001c0001t0003g0302 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.349-4488G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050150 | ||||||
| chr1:119050213
|
G | C | 8 | a0002c0002t0002g0132a0002c0002t0002g0135a0002c0002t0002g0136others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-4551C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050213 | ||||||
| chr1:119050342
|
T | C | 2 | a0001c0001t0006g0285a0001c0001t0006g0320 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.349-4680A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050342 | ||||||
| chr1:119050582
|
C | G | 67 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(64): Show | 70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.349-4920G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050582 | ||||||
| chr1:119050620
|
C | G | 1 | a0001c0001t0007g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.349-4958G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050620 | ||||||
| chr1:119050645
|
T | G | 67 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(64): Show | 70 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.349-4983A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050645 | ||||||
| chr1:119050651
|
G | A | 4 | a0001c0001t0006g0158a0001c0001t0006g0159a0001c0001t0006g0160others(1): Show | 4 | HG02056.hp2 HG02071.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-4989C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050651 | ||||||
| chr1:119050678
|
T | C | 71 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(68): Show | 74 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.349-5016A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050678 | ||||||
| chr1:119050683
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.349-5021A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050683 | ||||||
| chr1:119050776
|
C | T | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.349-5114G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119050776 | ||||||
| chr1:119051021
|
A | G | 77 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(74): Show | 80 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.349-5359T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051021 | ||||||
| chr1:119051036
|
T | A | 71 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0022others(68): Show | 74 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.349-5374A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051036 | ||||||
| chr1:119051188
|
G | T | 8 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(5): Show | 8 | HG00408.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-5526C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051188 | ||||||
| chr1:119051198
|
A | T | 74 | a0001c0001t0001g0141a0001c0001t0005g0117a0001c0001t0005g0145others(71): Show | 80 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.349-5536T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051198 | ||||||
| chr1:119051244
|
T | A | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | HG02080.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.349-5582A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051244 | ||||||
| chr1:119051288
|
T | C | 1 | a0002c0002t0002g0191 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.349-5626A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051288 | ||||||
| chr1:119051295
|
A | G | 82 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(79): Show | 85 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-5633T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051295 | ||||||
| chr1:119051332
|
C | T | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(10): Show | 13 | HG00558.hp1 HG00609.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-5670G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051332 | ||||||
| chr1:119051336
|
G | A | 82 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(79): Show | 85 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-5674C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051336 | ||||||
| chr1:119051337
|
T | A | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-5675A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051337 | ||||||
| chr1:119051582
|
A | G | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-5920T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051582 | ||||||
| chr1:119051613
|
A | G | 47 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0168others(44): Show | 50 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.349-5951T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051613 | ||||||
| chr1:119051721
|
C | A | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.349-6059G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051721 | ||||||
| chr1:119051762
|
A | AT | 34 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0073others(31): Show | 34 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.349-6101dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | ||||||
| chr1:119051762
|
A | ATT | 71 | a0001c0001t0001g0104a0001c0001t0001g0141a0001c0001t0005g0117others(68): Show | 77 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.349-6102_349-6101d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | ||||||
| chr1:119051762
|
AT | A | 14 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0098others(11): Show | 16 | HG00099.hp2 HG02080.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.349-6101delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | ||||||
| chr1:119051762
|
ATTT | A | 9 | a0001c0001t0004g0019a0001c0001t0004g0290a0001c0001t0005g0123others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-6103_349-6101d others(5): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | ||||||
| chr1:119051762
|
ATTTT | A | 58 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(55): Show | 61 | HG00408.hp1 HG00738.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.349-6104_349-6101d others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | ||||||
| chr1:119051762
|
ATTTTT | A | 14 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(11): Show | 14 | HG00558.hp1 HG00609.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.349-6105_349-6101d others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051762 | ||||||
| chr1:119051829
|
G | A | 2 | a0001c0001t0006g0010a0001c0001t0006g0315 | 3 | HG01070.hp1 HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.349-6167C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051829 | ||||||
| chr1:119051863
|
A | G | 1 | a0001c0001t0004g0330 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.349-6201T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119051863 | ||||||
| chr1:119052040
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(82): Show | 87 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.349-6378C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119052040 | ||||||
| chr1:119052373
|
T | C | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.349-6711A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119052373 | ||||||
| chr1:119052427
|
C | G | 1 | a0001c0001t0004g0019 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.349-6765G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119052427 | ||||||
| chr1:119052720
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.349-7058C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119052720 | ||||||
| chr1:119053036
|
A | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-7374T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053036 | ||||||
| chr1:119053097
|
G | A | 2 | a0001c0001t0003g0262a0001c0001t0003g0302 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.349-7435C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053097 | ||||||
| chr1:119053244
|
G | A | 1 | a0001c0001t0003g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.349-7582C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053244 | ||||||
| chr1:119053313
|
T | G | 74 | a0001c0001t0001g0141a0001c0001t0005g0117a0001c0001t0005g0145others(71): Show | 80 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.349-7651A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053313 | ||||||
| chr1:119053325
|
G | A | 3 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213 | 3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.349-7663C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053325 | ||||||
| chr1:119053326
|
C | T | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-7664G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053326 | ||||||
| chr1:119053408
|
A | C | 10 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.349-7746T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053408 | ||||||
| chr1:119053413
|
C | T | 1 | a0003c0004t0005g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.349-7751G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053413 | ||||||
| chr1:119053551
|
T | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-7889A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119053551 | ||||||
| chr1:119054015
|
C | T | 1 | a0002c0002t0002g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.349-8353G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054015 | ||||||
| chr1:119054206
|
C | T | 1 | a0001c0001t0012g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349-8544G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054206 | ||||||
| chr1:119054375
|
C | CAT | 7 | a0001c0001t0003g0255a0001c0001t0003g0257a0001c0001t0003g0261others(4): Show | 7 | HG00408.hp1 NA18941.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-8715_349-8714d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054375 | ||||||
| chr1:119054772
|
T | C | 82 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(79): Show | 85 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-9110A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054772 | ||||||
| chr1:119054811
|
A | G | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-9149T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054811 | ||||||
| chr1:119054948
|
G | A | 5 | a0001c0003t0009g0021a0001c0003t0009g0223a0001c0003t0009g0224others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-9286C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119054948 | ||||||
| chr1:119055050
|
A | G | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-9388T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055050 | ||||||
| chr1:119055075
|
G | T | 1 | a0001c0001t0005g0154 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.349-9413C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055075 | ||||||
| chr1:119055169
|
A | C | 82 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(79): Show | 85 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-9507T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055169 | ||||||
| chr1:119055414
|
G | A | 287 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(284): Show | 299 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(296): Show |
intron_variant | MODIFIER | c.349-9752C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055414 | ||||||
| chr1:119055568
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.349-9906C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055568 | ||||||
| chr1:119055682
|
CAAGAAAG others(6): Show |
C | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-10033_349-1002 others(17): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055682 | ||||||
| chr1:119055717
|
G | T | 2 | a0002c0002t0002g0143a0002c0002t0002g0144 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.349-10055C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119055717 | ||||||
| chr1:119056011
|
C | CT | 129 | a0001c0001t0001g0079a0001c0001t0001g0101a0001c0001t0001g0141others(126): Show | 138 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.349-10350dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056011 | ||||||
| chr1:119056011
|
C | CTT | 9 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(6): Show | 9 | HG01433.hp2 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-10351_349-1035 others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056011 | ||||||
| chr1:119056186
|
A | AT | 55 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0066others(52): Show | 55 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.349-10525dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056186 | ||||||
| chr1:119056186
|
A | ATT | 7 | a0001c0001t0004g0023a0001c0001t0004g0171a0001c0001t0007g0201others(4): Show | 7 | HG00609.hp1 HG02145.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-10526_349-1052 others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056186 | ||||||
| chr1:119056186
|
AT | A | 41 | a0001c0001t0001g0102a0001c0001t0004g0011a0001c0001t0004g0012others(38): Show | 44 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.349-10525delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056186 | ||||||
| chr1:119056365
|
A | G | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(10): Show | 13 | HG00558.hp1 HG00609.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-10703T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056365 | ||||||
| chr1:119056409
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.349-10747G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056409 | ||||||
| chr1:119056426
|
TAAC | T | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-10767_349-1076 others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056426 | ||||||
| chr1:119056504
|
A | T | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-10842T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056504 | ||||||
| chr1:119056536
|
AAT | A | 84 | a0001c0001t0003g0274a0001c0001t0004g0011a0001c0001t0004g0012others(81): Show | 87 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.349-10876_349-1087 others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056536 | ||||||
| chr1:119056584
|
C | T | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-10922G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056584 | ||||||
| chr1:119056605
|
C | T | 1 | a0001c0003t0007g0218 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.349-10943G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056605 | ||||||
| chr1:119056665
|
A | C | 8 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(5): Show | 8 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-11003T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056665 | ||||||
| chr1:119056674
|
C | T | 5 | a0001c0001t0003g0009a0001c0001t0003g0240a0001c0001t0003g0241others(2): Show | 6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-11012G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056674 | ||||||
| chr1:119056690
|
T | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(99): Show | 104 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.349-11028A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056690 | ||||||
| chr1:119056920
|
G | A | 1 | a0001c0001t0003g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.349-11258C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119056920 | ||||||
| chr1:119057142
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.349-11480A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057142 | ||||||
| chr1:119057185
|
C | T | 58 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(55): Show | 64 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.349-11523G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057185 | ||||||
| chr1:119057205
|
G | A | 1 | a0001c0001t0007g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.349-11543C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057205 | ||||||
| chr1:119057209
|
G | C | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-11547C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057209 | ||||||
| chr1:119057347
|
C | T | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-11685G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057347 | ||||||
| chr1:119057552
|
G | A | 22 | a0001c0001t0006g0010a0001c0001t0006g0158a0001c0001t0006g0159others(19): Show | 23 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.349-11890C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057552 | ||||||
| chr1:119057561
|
G | A | 1 | a0002c0002t0002g0124 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.349-11899C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057561 | ||||||
| chr1:119057644
|
G | A | 2 | a0002c0002t0002g0187a0002c0002t0002g0190 | 2 | NA18747.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.349-11982C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057644 | ||||||
| chr1:119057661
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349-11999C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057661 | ||||||
| chr1:119057664
|
C | T | 47 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0168others(44): Show | 50 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.349-12002G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057664 | ||||||
| chr1:119057738
|
C | T | 5 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(2): Show | 5 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-12076G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057738 | ||||||
| chr1:119057845
|
A | T | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-12183T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119057845 | ||||||
| chr1:119058189
|
C | T | 82 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(79): Show | 85 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.349-12527G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058189 | ||||||
| chr1:119058286
|
C | A | 1 | a0001c0001t0005g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.349-12624G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058286 | ||||||
| chr1:119058307
|
C | CT | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(232): Show | 246 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.349-12646dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058307 | ||||||
| chr1:119058307
|
C | CTT | 14 | a0001c0001t0003g0056a0001c0001t0005g0154a0001c0001t0008g0276others(11): Show | 14 | HG02004.hp2 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-12647_349-1264 others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058307 | ||||||
| chr1:119058322
|
T | A | 10 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(7): Show | 10 | HG00408.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.349-12660A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058322 | ||||||
| chr1:119058322
|
T | TA | 73 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(70): Show | 76 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.349-12661dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058322 | ||||||
| chr1:119058332
|
G | A | 1 | a0001c0001t0006g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.349-12670C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058332 | ||||||
| chr1:119058397
|
G | A | 75 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(72): Show | 78 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.349-12735C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058397 | ||||||
| chr1:119058408
|
TA | T | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-12747delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058408 | ||||||
| chr1:119058468
|
C | T | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-12806G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058468 | ||||||
| chr1:119058516
|
A | T | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-12854T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058516 | ||||||
| chr1:119058545
|
G | A | 79 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(76): Show | 82 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.349-12883C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058545 | ||||||
| chr1:119058554
|
C | T | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-12892G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058554 | ||||||
| chr1:119058662
|
G | T | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13000C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058662 | ||||||
| chr1:119058668
|
A | G | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13006T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058668 | ||||||
| chr1:119058714
|
G | A | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13052C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058714 | ||||||
| chr1:119058753
|
G | A | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13091C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058753 | ||||||
| chr1:119058758
|
G | A | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13096C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058758 | ||||||
| chr1:119058775
|
A | G | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13113T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058775 | ||||||
| chr1:119058868
|
C | T | 1 | a0002c0002t0002g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349-13206G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058868 | ||||||
| chr1:119058930
|
G | A | 1 | a0001c0003t0007g0219 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.349-13268C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119058930 | ||||||
| chr1:119059136
|
G | A | 1 | a0001c0001t0007g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.349-13474C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059136 | ||||||
| chr1:119059179
|
G | A | 4 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(1): Show | 4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-13517C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059179 | ||||||
| chr1:119059187
|
T | G | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-13525A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059187 | ||||||
| chr1:119059249
|
G | C | 1 | a0001c0001t0007g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.349-13587C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059249 | ||||||
| chr1:119059441
|
C | A | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | HG02080.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.349-13779G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059441 | ||||||
| chr1:119059535
|
C | T | 18 | a0001c0001t0007g0020a0001c0003t0007g0218a0001c0003t0007g0219others(15): Show | 18 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.349-13873G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059535 | ||||||
| chr1:119059591
|
C | A | 1 | a0005c0008t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.349-13929G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059591 | ||||||
| chr1:119059592
|
A | G | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-13930T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059592 | ||||||
| chr1:119059690
|
G | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-14028C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059690 | ||||||
| chr1:119059758
|
A | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.349-14096T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059758 | ||||||
| chr1:119059792
|
T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(96): Show | 101 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.349-14130A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059792 | ||||||
| chr1:119059981
|
T | C | 10 | a0001c0001t0007g0055a0001c0001t0007g0201a0001c0001t0007g0203others(7): Show | 10 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.349-14319A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119059981 | ||||||
| chr1:119060353
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.349-14691G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060353 | ||||||
| chr1:119060402
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349-14740G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060402 | ||||||
| chr1:119060444
|
C | A | 83 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(80): Show | 86 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.349-14782G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060444 | ||||||
| chr1:119060479
|
A | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0057a0001c0001t0001g0080others(3): Show | 6 | NA18946.hp2 NA18948.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-14817T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060479 | ||||||
| chr1:119060653
|
T | C | 1 | a0006c0009t0003g0326 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.349-14991A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060653 | ||||||
| chr1:119060686
|
C | T | 1 | a0001c0001t0003g0302 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.349-15024G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060686 | ||||||
| chr1:119060699
|
T | C | 86 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(83): Show | 89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.349-15037A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060699 | ||||||
| chr1:119060782
|
A | G | 86 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(83): Show | 89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.349-15120T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060782 | ||||||
| chr1:119060794
|
T | C | 78 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(75): Show | 81 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.349-15132A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060794 | ||||||
| chr1:119060807
|
G | C | 5 | a0001c0001t0003g0247a0001c0001t0003g0248a0001c0001t0003g0249others(2): Show | 5 | HG00408.hp2 HG00642.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-15145C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060807 | ||||||
| chr1:119060917
|
C | T | 4 | a0001c0001t0003g0231a0001c0001t0003g0232a0001c0001t0003g0233others(1): Show | 4 | HG00735.hp2 HG00741.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-15255G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119060917 | ||||||
| chr1:119061077
|
A | T | 86 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(83): Show | 89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.348+15273T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061077 | ||||||
| chr1:119061280
|
G | A | 3 | a0001c0001t0008g0276a0001c0001t0008g0278a0001c0001t0008g0283 | 3 | HG02145.hp2 HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.348+15070C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061280 | ||||||
| chr1:119061485
|
T | C | 1 | a0001c0001t0005g0145 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.348+14865A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061485 | ||||||
| chr1:119061637
|
A | C | 27 | a0001c0001t0007g0055a0001c0001t0007g0201a0001c0001t0007g0203others(24): Show | 27 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.348+14713T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061637 | ||||||
| chr1:119061755
|
T | C | 1 | a0001c0001t0005g0157 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.348+14595A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061755 | ||||||
| chr1:119061827
|
C | T | 3 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213 | 3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.348+14523G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061827 | ||||||
| chr1:119061845
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0103 | 2 | NA18948.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.348+14505C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061845 | ||||||
| chr1:119061850
|
A | T | 86 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(83): Show | 89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.348+14500T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119061850 | ||||||
| chr1:119062032
|
T | C | 86 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(83): Show | 89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.348+14318A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062032 | ||||||
| chr1:119062196
|
G | A | 1 | a0001c0001t0007g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.348+14154C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062196 | ||||||
| chr1:119062321
|
G | A | 1 | a0001c0001t0006g0334 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.348+14029C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062321 | ||||||
| chr1:119062399
|
G | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+13951C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062399 | ||||||
| chr1:119062431
|
A | T | 78 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(75): Show | 81 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.348+13919T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062431 | ||||||
| chr1:119062466
|
T | TA | 73 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0168others(70): Show | 76 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+13883dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062466 | ||||||
| chr1:119062468
|
A | T | 1 | a0002c0002t0002g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.348+13882T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062468 | ||||||
| chr1:119062573
|
A | C | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.348+13777T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062573 | ||||||
| chr1:119062595
|
C | T | 54 | a0001c0001t0001g0141a0001c0001t0005g0263a0001c0001t0005g0264others(51): Show | 60 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.348+13755G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062595 | ||||||
| chr1:119062604
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(279): Show | 293 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.348+13746A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062604 | ||||||
| chr1:119062679
|
A | G | 2 | a0001c0001t0004g0023a0001c0001t0004g0024 | 2 | NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.348+13671T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062679 | ||||||
| chr1:119062771
|
G | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+13579C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062771 | ||||||
| chr1:119062776
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.348+13574A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062776 | ||||||
| chr1:119062829
|
C | T | 1 | a0001c0003t0007g0297 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.348+13521G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062829 | ||||||
| chr1:119062864
|
G | A | 4 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(1): Show | 4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+13486C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119062864 | ||||||
| chr1:119063249
|
G | A | 1 | a0001c0001t0007g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.348+13101C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063249 | ||||||
| chr1:119063374
|
A | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(288): Show | 303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.348+12976T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063374 | ||||||
| chr1:119063507
|
T | C | 74 | a0001c0001t0001g0141a0001c0001t0005g0117a0001c0001t0005g0145others(71): Show | 80 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.348+12843A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063507 | ||||||
| chr1:119063547
|
A | G | 1 | a0001c0001t0006g0314 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.348+12803T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063547 | ||||||
| chr1:119063638
|
C | T | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348+12712G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063638 | ||||||
| chr1:119063656
|
A | C | 1 | a0001c0001t0007g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.348+12694T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063656 | ||||||
| chr1:119063676
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.348+12674C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063676 | ||||||
| chr1:119063760
|
C | T | 3 | a0001c0001t0005g0162a0001c0001t0005g0165a0001c0001t0005g0167 | 3 | NA18946.hp1 NA18959.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.348+12590G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063760 | ||||||
| chr1:119063980
|
T | C | 1 | a0001c0001t0012g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.348+12370A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063980 | ||||||
| chr1:119063989
|
C | T | 10 | a0001c0001t0001g0141a0002c0002t0002g0122a0002c0002t0002g0126others(7): Show | 10 | HG02027.hp2 HG02129.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+12361G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063989 | ||||||
| chr1:119063994
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.348+12356C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119063994 | ||||||
| chr1:119064128
|
C | T | 1 | a0002c0002t0002g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348+12222G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064128 | ||||||
| chr1:119064129
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0064 | 3 | NA18960.hp2 NA18994.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.348+12221C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064129 | ||||||
| chr1:119064196
|
T | TG | 86 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(83): Show | 89 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.348+12153dupC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064196 | ||||||
| chr1:119064337
|
G | T | 82 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0017others(79): Show | 85 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.348+12013C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064337 | ||||||
| chr1:119064364
|
G | A | 1 | a0001c0003t0007g0254 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.348+11986C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064364 | ||||||
| chr1:119064382
|
T | C | 5 | a0001c0001t0004g0011a0001c0001t0004g0335a0001c0001t0004g0336others(2): Show | 6 | HG01884.hp1 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+11968A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064382 | ||||||
| chr1:119064570
|
T | C | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(287): Show | 302 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.348+11780A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064570 | ||||||
| chr1:119064571
|
G | A | 74 | a0001c0001t0001g0141a0001c0001t0005g0117a0001c0001t0005g0145others(71): Show | 80 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.348+11779C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064571 | ||||||
| chr1:119064596
|
G | A | 4 | a0001c0001t0005g0148a0001c0001t0005g0149a0001c0001t0005g0150others(1): Show | 4 | HG01167.hp2 HG01358.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+11754C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064596 | ||||||
| chr1:119064693
|
G | A | 13 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(10): Show | 13 | HG00558.hp1 HG00609.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.348+11657C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064693 | ||||||
| chr1:119064727
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.348+11623C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064727 | ||||||
| chr1:119064784
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.348+11566G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064784 | ||||||
| chr1:119064792
|
G | A | 1 | a0002c0002t0002g0134 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.348+11558C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064792 | ||||||
| chr1:119064830
|
C | T | 15 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(12): Show | 15 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.348+11520G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064830 | ||||||
| chr1:119064868
|
T | TCAAAAAT others(314): Show |
1 | a0001c0001t0004g0019 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.348+11481_348+1148 others(325): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064868 | ||||||
| chr1:119064868
|
T | TCAAAAAT others(327): Show |
1 | a0001c0001t0004g0017 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.348+11481_348+1148 others(338): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064868 | ||||||
| chr1:119064868
|
T | TCAAAAAT others(328): Show |
1 | a0001c0001t0004g0018 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.348+11481_348+1148 others(339): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119064868 | ||||||
| chr1:119065069
|
A | T | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+11281T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065069 | ||||||
| chr1:119065073
|
A | C | 1 | a0001c0001t0005g0146 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.348+11277T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065073 | ||||||
| chr1:119065158
|
G | A | 1 | a0002c0002t0002g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.348+11192C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065158 | ||||||
| chr1:119065192
|
G | GA | 10 | a0001c0001t0007g0055a0001c0001t0007g0201a0001c0001t0007g0203others(7): Show | 10 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+11157dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065192 | ||||||
| chr1:119065211
|
A | C | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348+11139T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065211 | ||||||
| chr1:119065453
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.348+10897C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065453 | ||||||
| chr1:119065576
|
A | G | 3 | a0001c0001t0003g0008a0001c0001t0003g0229a0001c0001t0003g0230 | 4 | NA19001.hp1 NA19004.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+10774T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065576 | ||||||
| chr1:119065599
|
C | T | 2 | a0001c0006t0004g0025a0001c0006t0004g0175 | 2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.348+10751G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065599 | ||||||
| chr1:119065626
|
C | T | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+10724G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065626 | ||||||
| chr1:119065634
|
C | CA | 22 | a0001c0001t0001g0043a0001c0001t0003g0242a0001c0001t0003g0246others(19): Show | 22 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.348+10715dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065634 | ||||||
| chr1:119065634
|
CA | C | 92 | a0001c0001t0001g0077a0001c0001t0004g0011a0001c0001t0004g0012others(89): Show | 95 | HG00558.hp1 HG00609.hp1 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.348+10715delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119065634 | ||||||
| chr1:119066109
|
T | C | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.348+10241A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066109 | ||||||
| chr1:119066136
|
C | A | 2 | a0001c0001t0006g0285a0001c0001t0006g0320 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.348+10214G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066136 | ||||||
| chr1:119066203
|
T | C | 25 | a0001c0001t0001g0032a0001c0001t0001g0080a0001c0001t0004g0017others(22): Show | 25 | HG00621.hp1 HG01074.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.348+10147A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066203 | ||||||
| chr1:119066253
|
G | A | 1 | a0001c0001t0006g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.348+10097C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066253 | ||||||
| chr1:119066260
|
A | G | 2 | a0001c0006t0004g0025a0001c0006t0004g0175 | 2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.348+10090T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066260 | ||||||
| chr1:119066273
|
C | T | 2 | a0001c0006t0004g0025a0001c0006t0004g0175 | 2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.348+10077G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066273 | ||||||
| chr1:119066289
|
T | C | 1 | a0002c0002t0002g0181 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.348+10061A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066289 | ||||||
| chr1:119066292
|
T | C | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(291): Show | 307 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.348+10058A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066292 | ||||||
| chr1:119066295
|
G | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(181): Show | 193 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.348+10055C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066295 | ||||||
| chr1:119066346
|
T | C | 27 | a0001c0001t0001g0034a0001c0001t0001g0178a0001c0001t0004g0022others(24): Show | 27 | HG00558.hp1 HG00609.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.348+10004A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066346 | ||||||
| chr1:119066451
|
A | C | 2 | a0001c0001t0004g0305a0001c0001t0004g0306 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.348+9899T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066451 | ||||||
| chr1:119066477
|
C | CA | 16 | a0001c0001t0001g0043a0001c0001t0001g0073a0001c0001t0001g0085others(13): Show | 16 | HG00621.hp2 HG01123.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.348+9872dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066477 | ||||||
| chr1:119066477
|
CA | C | 65 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0077others(62): Show | 71 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.348+9872delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066477 | ||||||
| chr1:119066523
|
ATAATG | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0333a0006c0009t0003g0326 | 4 | NA18612.hp1 NA18968.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+9822_348+9826d others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066523 | ||||||
| chr1:119066565
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0014g0063 | 2 | HG02602.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.348+9785G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066565 | ||||||
| chr1:119066705
|
G | T | 2 | a0002c0002t0011g0129a0002c0002t0011g0130 | 2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.348+9645C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066705 | ||||||
| chr1:119066741
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.348+9609A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066741 | ||||||
| chr1:119066751
|
A | G | 1 | a0002c0002t0002g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.348+9599T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119066751 | ||||||
| chr1:119067129
|
C | CA | 77 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(74): Show | 81 | HG00438.hp1 HG00621.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.348+9220dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119067129 | ||||||
| chr1:119067560
|
C | T | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+8790G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119067560 | ||||||
| chr1:119067647
|
T | C | 42 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0005others(39): Show | 47 | HG00423.hp2 HG01257.hp2 HG01258.hp1 others(44): Show |
intron_variant | MODIFIER | c.348+8703A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119067647 | ||||||
| chr1:119067811
|
A | ATT | 55 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(52): Show | 61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.348+8537_348+8538d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119067811 | ||||||
| chr1:119067989
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.348+8361C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119067989 | ||||||
| chr1:119068001
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.348+8349A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068001 | ||||||
| chr1:119068141
|
G | A | 56 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(53): Show | 62 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.348+8209C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068141 | ||||||
| chr1:119068164
|
C | T | 55 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(52): Show | 59 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.348+8186G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068164 | ||||||
| chr1:119068226
|
C | G | 56 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(53): Show | 62 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.348+8124G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068226 | ||||||
| chr1:119068579
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.348+7771G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068579 | ||||||
| chr1:119068606
|
G | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+7744C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068606 | ||||||
| chr1:119068728
|
A | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0035others(18): Show | 22 | HG00621.hp2 HG00673.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.348+7622T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068728 | ||||||
| chr1:119068808
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.348+7542C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068808 | ||||||
| chr1:119068825
|
A | ACT | 150 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(147): Show | 160 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.348+7523_348+7524d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068825 | ||||||
| chr1:119068825
|
A | ACTCT | 8 | a0002c0002t0002g0132a0002c0002t0002g0135a0002c0002t0002g0136others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+7521_348+7524d others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068825 | ||||||
| chr1:119068841
|
A | T | 154 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(151): Show | 164 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.348+7509T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068841 | ||||||
| chr1:119068854
|
T | C | 154 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(151): Show | 164 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.348+7496A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068854 | ||||||
| chr1:119068854
|
T | TAC | 3 | a0001c0001t0001g0053a0001c0003t0007g0219a0001c0003t0007g0220 | 3 | HG01978.hp1 HG02129.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.348+7494_348+7495d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068854 | ||||||
| chr1:119068856
|
C | T | 154 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(151): Show | 164 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.348+7494G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119068856 | ||||||
| chr1:119069378
|
C | T | 56 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(53): Show | 62 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.348+6972G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119069378 | ||||||
| chr1:119069489
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+6861A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119069489 | ||||||
| chr1:119069782
|
G | C | 1 | a0001c0001t0003g0107 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.348+6568C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119069782 | ||||||
| chr1:119070009
|
C | T | 162 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(159): Show | 172 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.348+6341G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070009 | ||||||
| chr1:119070478
|
G | C | 1 | a0001c0001t0006g0309 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.348+5872C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070478 | ||||||
| chr1:119070605
|
AG | A | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(336): Show | 353 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.348+5744delC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070605 | ||||||
| chr1:119070744
|
A | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0099 | 2 | NA18991.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.348+5606T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070744 | ||||||
| chr1:119070806
|
A | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(83): Show | 88 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.348+5544T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070806 | ||||||
| chr1:119070935
|
C | T | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 6 | HG01258.hp2 NA18939.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+5415G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119070935 | ||||||
| chr1:119071106
|
C | T | 1 | a0001c0001t0010g0300 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.348+5244G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071106 | ||||||
| chr1:119071318
|
G | A | 162 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(159): Show | 172 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.348+5032C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071318 | ||||||
| chr1:119071448
|
T | G | 47 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(44): Show | 51 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.348+4902A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071448 | ||||||
| chr1:119071496
|
G | A | 1 | a0001c0001t0005g0166 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.348+4854C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071496 | ||||||
| chr1:119071545
|
T | C | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+4805A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071545 | ||||||
| chr1:119071648
|
T | A | 4 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+4702A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071648 | ||||||
| chr1:119071714
|
A | T | 55 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(52): Show | 59 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.348+4636T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071714 | ||||||
| chr1:119071761
|
A | G | 5 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(2): Show | 5 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+4589T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119071761 | ||||||
| chr1:119072020
|
A | G | 1 | a0002c0002t0002g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.348+4330T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072020 | ||||||
| chr1:119072025
|
T | C | 1 | a0001c0006t0004g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.348+4325A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072025 | ||||||
| chr1:119072060
|
T | C | 1 | a0001c0001t0006g0320 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.348+4290A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072060 | ||||||
| chr1:119072232
|
A | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | NA18944.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.348+4118T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072232 | ||||||
| chr1:119072352
|
A | T | 1 | a0001c0001t0004g0339 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.348+3998T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072352 | ||||||
| chr1:119072500
|
G | A | 1 | a0001c0001t0006g0331 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.348+3850C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072500 | ||||||
| chr1:119072642
|
T | C | 8 | a0002c0002t0002g0132a0002c0002t0002g0135a0002c0002t0002g0136others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+3708A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072642 | ||||||
| chr1:119072838
|
CT | C | 98 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(95): Show | 102 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.348+3511delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119072838 | ||||||
| chr1:119073036
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.348+3314T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073036 | ||||||
| chr1:119073153
|
CAAAAAAG others(7): Show |
C | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(85): Show | 90 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.348+3183_348+3196d others(16): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073153 | ||||||
| chr1:119073160
|
G | GA | 6 | a0001c0001t0003g0262a0001c0001t0004g0168a0001c0001t0005g0263others(3): Show | 6 | HG00408.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+3189dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073160 | ||||||
| chr1:119073245
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.348+3105A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073245 | ||||||
| chr1:119073333
|
A | C | 41 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(38): Show | 45 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.348+3017T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073333 | ||||||
| chr1:119073595
|
G | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+2755C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073595 | ||||||
| chr1:119073622
|
A | G | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+2728T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073622 | ||||||
| chr1:119073655
|
A | G | 97 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(94): Show | 101 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.348+2695T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073655 | ||||||
| chr1:119073789
|
A | G | 1 | a0002c0002t0002g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.348+2561T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073789 | ||||||
| chr1:119073817
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.348+2533A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073817 | ||||||
| chr1:119073885
|
T | C | 1 | a0001c0001t0004g0022 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.348+2465A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119073885 | ||||||
| chr1:119074183
|
T | C | 1 | a0001c0001t0004g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.348+2167A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074183 | ||||||
| chr1:119074250
|
G | C | 1 | a0001c0001t0006g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.348+2100C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074250 | ||||||
| chr1:119074315
|
G | A | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | HG02080.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.348+2035C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074315 | ||||||
| chr1:119074321
|
C | T | 17 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(14): Show | 17 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.348+2029G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074321 | ||||||
| chr1:119074504
|
C | T | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.348+1846G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074504 | ||||||
| chr1:119074684
|
C | T | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348+1666G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074684 | ||||||
| chr1:119074826
|
C | A | 1 | a0001c0001t0006g0314 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.348+1524G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119074826 | ||||||
| chr1:119075154
|
G | GTATATAT others(5): Show |
3 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0266 | 3 | NA18962.hp1 NA19005.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.348+1195_348+1196i others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075154 | ||||||
| chr1:119075154
|
G | GTATATAT others(7): Show |
37 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(34): Show | 41 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.348+1195_348+1196i others(16): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075154 | ||||||
| chr1:119075154
|
G | GTATATAT others(9): Show |
18 | a0001c0001t0005g0265a0002c0002t0002g0005a0002c0002t0002g0007others(15): Show | 20 | HG00408.hp1 HG02055.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.348+1195_348+1196i others(18): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075154 | ||||||
| chr1:119075154
|
G | GTATATAT others(11): Show |
2 | a0002c0002t0002g0121a0002c0002t0002g0191 | 2 | HG02040.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.348+1195_348+1196i others(20): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075154 | ||||||
| chr1:119075165
|
C | T | 60 | a0001c0001t0001g0141a0001c0001t0005g0263a0001c0001t0005g0264others(57): Show | 66 | HG00408.hp1 HG00423.hp2 HG01175.hp1 others(63): Show |
intron_variant | MODIFIER | c.348+1185G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075165 | ||||||
| chr1:119075215
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.348+1135G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075215 | ||||||
| chr1:119075733
|
G | T | 1 | a0001c0007t0004g0014 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.348+617C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075733 | ||||||
| chr1:119075895
|
TAA | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(81): Show | 86 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.348+453_348+454del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075895 | ||||||
| chr1:119075981
|
G | T | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.348+369C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119075981 | ||||||
| chr1:119076057
|
T | G | 48 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(45): Show | 54 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(51): Show |
intron_variant | MODIFIER | c.348+293A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119076057 | ||||||
| chr1:119076069
|
T | A | 1 | a0001c0001t0001g0071 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.348+281A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119076069 | ||||||
| chr1:119076296
|
T | C | 1 | a0001c0001t0005g0146 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.348+54A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119076296 | ||||||
| chr1:119076307
|
T | C | 2 | a0001c0001t0006g0318a0001c0001t0006g0332 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.348+43A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 2/5 | chr1 | 119076307 | ||||||
| chr1:119076731
|
A | G | 2 | a0001c0001t0006g0285a0001c0001t0006g0320 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.91-124T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076731 | ||||||
| chr1:119076798
|
T | C | 2 | a0001c0001t0004g0168a0001c0001t0008g0338 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.91-191A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076798 | ||||||
| chr1:119076825
|
G | T | 165 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(162): Show | 175 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.91-218C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076825 | ||||||
| chr1:119076888
|
C | T | 28 | a0001c0001t0007g0055a0001c0001t0007g0201a0001c0001t0007g0203others(25): Show | 28 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.91-281G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076888 | ||||||
| chr1:119076889
|
C | T | 6 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0305others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-282G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076889 | ||||||
| chr1:119076890
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.91-283C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119076890 | ||||||
| chr1:119077020
|
G | C | 293 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(290): Show | 306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.91-413C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077020 | ||||||
| chr1:119077031
|
C | A | 56 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(53): Show | 62 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.91-424G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077031 | ||||||
| chr1:119077051
|
T | C | 6 | a0001c0001t0003g0302a0001c0001t0004g0301a0001c0001t0010g0292others(3): Show | 6 | HG02818.hp2 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-444A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077051 | ||||||
| chr1:119077137
|
C | CAAAAAAA others(4): Show |
62 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0141others(59): Show | 68 | HG00408.hp1 HG00423.hp2 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.91-541_91-531dupTT others(9): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077137 | ||||||
| chr1:119077137
|
C | CAAAAAAA others(5): Show |
114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.91-531_91-530insTT others(10): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077137 | ||||||
| chr1:119077137
|
C | CAAAAAAA others(6): Show |
94 | a0001c0001t0001g0032a0001c0001t0001g0066a0001c0001t0001g0075others(91): Show | 98 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.91-531_91-530insTT others(11): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077137 | ||||||
| chr1:119077137
|
C | CAAAAAAA others(7): Show |
7 | a0001c0001t0004g0037a0001c0001t0004g0177a0001c0001t0004g0325others(4): Show | 7 | HG01168.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.91-531_91-530insTT others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077137 | ||||||
| chr1:119077157
|
T | C | 1 | a0001c0001t0003g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.91-550A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077157 | ||||||
| chr1:119077207
|
A | G | 14 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(11): Show | 14 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.91-600T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077207 | ||||||
| chr1:119077326
|
C | T | 1 | a0001c0001t0008g0338 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.91-719G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077326 | ||||||
| chr1:119077584
|
C | T | 56 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(53): Show | 62 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.91-977G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077584 | ||||||
| chr1:119077593
|
C | T | 1 | a0001c0001t0003g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.91-986G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077593 | ||||||
| chr1:119077630
|
T | A | 2 | a0002c0002t0002g0195a0002c0002t0002g0198 | 2 | NA18963.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.91-1023A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077630 | ||||||
| chr1:119077658
|
T | C | 1 | a0001c0001t0004g0336 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.91-1051A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077658 | ||||||
| chr1:119077734
|
C | T | 293 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(290): Show | 306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.91-1127G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119077734 | ||||||
| chr1:119078183
|
C | T | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-1576G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078183 | ||||||
| chr1:119078213
|
A | G | 1 | a0001c0001t0008g0280 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.91-1606T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078213 | ||||||
| chr1:119078591
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.91-1984T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078591 | ||||||
| chr1:119078718
|
C | T | 56 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(53): Show | 62 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.91-2111G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078718 | ||||||
| chr1:119078887
|
T | C | 28 | a0001c0001t0007g0055a0001c0001t0007g0201a0001c0001t0007g0203others(25): Show | 28 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.91-2280A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078887 | ||||||
| chr1:119078897
|
C | CGT | 35 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(32): Show | 37 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.91-2292_91-2291dup others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078897 | ||||||
| chr1:119078947
|
GAC | G | 162 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(159): Show | 172 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.91-2342_91-2341del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119078947 | ||||||
| chr1:119079058
|
A | G | 4 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(1): Show | 4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-2451T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119079058 | ||||||
| chr1:119079169
|
G | A | 56 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(53): Show | 62 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.91-2562C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119079169 | ||||||
| chr1:119079271
|
T | C | 55 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(52): Show | 59 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.91-2664A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119079271 | ||||||
| chr1:119079426
|
T | C | 1 | a0001c0001t0004g0294 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91-2819A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119079426 | ||||||
| chr1:119079861
|
T | C | 3 | a0002c0002t0002g0142a0002c0002t0011g0129a0002c0002t0011g0130 | 3 | HG02280.hp2 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.91-3254A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119079861 | ||||||
| chr1:119080198
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.91-3591C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119080198 | ||||||
| chr1:119080335
|
G | A | 1 | a0001c0001t0005g0166 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.91-3728C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119080335 | ||||||
| chr1:119081054
|
C | G | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91-4447G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081054 | ||||||
| chr1:119081178
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.91-4571G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081178 | ||||||
| chr1:119081275
|
G | A | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-4668C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081275 | ||||||
| chr1:119081298
|
A | G | 56 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(53): Show | 62 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.91-4691T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081298 | ||||||
| chr1:119081325
|
A | G | 1 | a0002c0002t0002g0114 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.91-4718T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081325 | ||||||
| chr1:119081540
|
T | C | 105 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(102): Show | 109 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.91-4933A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081540 | ||||||
| chr1:119081804
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.91-5197C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119081804 | ||||||
| chr1:119082017
|
T | G | 2 | a0001c0001t0004g0305a0001c0001t0004g0306 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.91-5410A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082017 | ||||||
| chr1:119082028
|
A | G | 5 | a0001c0001t0003g0009a0001c0001t0003g0240a0001c0001t0003g0241others(2): Show | 6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-5421T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082028 | ||||||
| chr1:119082055
|
A | G | 14 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(11): Show | 14 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.91-5448T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082055 | ||||||
| chr1:119082210
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.91-5603A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082210 | ||||||
| chr1:119082326
|
C | T | 1 | a0001c0001t0008g0279 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.91-5719G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082326 | ||||||
| chr1:119082344
|
C | T | 10 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-5737G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082344 | ||||||
| chr1:119082366
|
T | G | 1 | a0001c0001t0003g0238 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.91-5759A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082366 | ||||||
| chr1:119082373
|
C | G | 162 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(159): Show | 172 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.91-5766G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082373 | ||||||
| chr1:119082561
|
TG | T | 11 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(8): Show | 11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.91-5955delC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082561 | ||||||
| chr1:119082940
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0086a0001c0001t0001g0102 | 3 | NA18939.hp1 NA18955.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.91-6333C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082940 | ||||||
| chr1:119082971
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.91-6364C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119082971 | ||||||
| chr1:119083018
|
CA | C | 5 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0305others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-6412delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083018 | ||||||
| chr1:119083058
|
G | T | 8 | a0002c0002t0002g0119a0002c0002t0002g0120a0002c0002t0002g0121others(5): Show | 8 | NA18939.hp2 NA18940.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.91-6451C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083058 | ||||||
| chr1:119083119
|
C | T | 17 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(14): Show | 17 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.91-6512G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083119 | ||||||
| chr1:119083154
|
G | A | 2 | a0002c0002t0002g0143a0002c0002t0002g0144 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.91-6547C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083154 | ||||||
| chr1:119083186
|
G | A | 3 | a0001c0001t0003g0008a0001c0001t0003g0229a0001c0001t0003g0230 | 4 | NA19001.hp1 NA19004.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-6579C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083186 | ||||||
| chr1:119083268
|
T | A | 3 | a0001c0001t0003g0268a0001c0001t0003g0269a0001c0001t0003g0271 | 3 | HG01361.hp2 HG01515.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.91-6661A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083268 | ||||||
| chr1:119083273
|
ACT | A | 6 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0305others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-6668_91-6667del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083273 | ||||||
| chr1:119083884
|
C | T | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-7277G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119083884 | ||||||
| chr1:119084181
|
A | AT | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(336): Show | 353 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.91-7575dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084181 | ||||||
| chr1:119084349
|
TAGAC | T | 11 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(8): Show | 11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.91-7746_91-7743del others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084349 | ||||||
| chr1:119084359
|
C | T | 1 | a0001c0003t0007g0218 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.91-7752G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084359 | ||||||
| chr1:119084437
|
A | G | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-7830T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084437 | ||||||
| chr1:119084502
|
C | A | 6 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0305others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-7895G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084502 | ||||||
| chr1:119084525
|
T | G | 56 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(53): Show | 62 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.91-7918A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084525 | ||||||
| chr1:119084604
|
C | T | 46 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(43): Show | 50 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.91-7997G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084604 | ||||||
| chr1:119084747
|
G | A | 1 | a0001c0001t0003g0268 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.91-8140C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084747 | ||||||
| chr1:119084811
|
T | C | 1 | a0002c0002t0002g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91-8204A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119084811 | ||||||
| chr1:119085056
|
C | T | 15 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(12): Show | 15 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-8449G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085056 | ||||||
| chr1:119085233
|
C | T | 162 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(159): Show | 172 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.91-8626G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085233 | ||||||
| chr1:119085331
|
T | C | 56 | a0001c0001t0001g0141a0002c0002t0002g0001a0002c0002t0002g0004others(53): Show | 62 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.91-8724A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085331 | ||||||
| chr1:119085375
|
C | A | 4 | a0001c0001t0004g0012a0001c0001t0004g0317a0001c0001t0004g0330others(1): Show | 5 | HG03490.hp1 HG03492.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-8768G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085375 | ||||||
| chr1:119085473
|
C | CT | 98 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(95): Show | 102 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.91-8867dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085473 | ||||||
| chr1:119085751
|
C | A | 1 | a0001c0001t0005g0264 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.91-9144G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085751 | ||||||
| chr1:119085833
|
C | T | 1 | a0002c0002t0002g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91-9226G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085833 | ||||||
| chr1:119085849
|
C | T | 6 | a0001c0001t0003g0302a0001c0001t0004g0301a0001c0001t0010g0292others(3): Show | 6 | HG02818.hp2 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-9242G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085849 | ||||||
| chr1:119085887
|
G | C | 6 | a0001c0001t0003g0302a0001c0001t0004g0301a0001c0001t0010g0292others(3): Show | 6 | HG02818.hp2 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-9280C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085887 | ||||||
| chr1:119085917
|
A | G | 2 | a0001c0001t0006g0318a0001c0001t0006g0332 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.91-9310T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085917 | ||||||
| chr1:119085979
|
C | A | 1 | a0001c0001t0008g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.91-9372G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119085979 | ||||||
| chr1:119086064
|
T | G | 6 | a0001c0001t0001g0043a0001c0001t0001g0067a0001c0001t0001g0073others(3): Show | 6 | HG01261.hp1 HG01934.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-9457A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086064 | ||||||
| chr1:119086100
|
T | A | 1 | a0001c0001t0001g0060 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.91-9493A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086100 | ||||||
| chr1:119086187
|
T | G | 1 | a0001c0001t0006g0329 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91-9580A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086187 | ||||||
| chr1:119086255
|
C | T | 5 | a0001c0001t0003g0231a0001c0001t0003g0232a0001c0001t0003g0233others(2): Show | 5 | HG00735.hp2 HG00741.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-9648G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086255 | ||||||
| chr1:119086414
|
C | G | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-9807G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086414 | ||||||
| chr1:119086849
|
G | A | 1 | a0001c0001t0008g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.91-10242C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086849 | ||||||
| chr1:119086926
|
T | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-10319A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086926 | ||||||
| chr1:119086948
|
G | C | 1 | a0001c0001t0004g0294 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91-10341C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119086948 | ||||||
| chr1:119087081
|
T | C | 276 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(273): Show | 288 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.91-10474A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087081 | ||||||
| chr1:119087160
|
T | C | 1 | a0001c0001t0006g0161 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.91-10553A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087160 | ||||||
| chr1:119087198
|
G | A | 46 | a0001c0001t0001g0141a0001c0001t0006g0158a0001c0001t0006g0159others(43): Show | 51 | HG00423.hp2 HG01257.hp2 HG01258.hp1 others(48): Show |
intron_variant | MODIFIER | c.91-10591C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087198 | ||||||
| chr1:119087210
|
A | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-10603T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087210 | ||||||
| chr1:119087326
|
C | T | 1 | a0001c0001t0006g0319 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.91-10719G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087326 | ||||||
| chr1:119087374
|
T | G | 6 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0001t0004g0305others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-10767A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087374 | ||||||
| chr1:119087924
|
A | T | 1 | a0001c0001t0006g0310 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.91-11317T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119087924 | ||||||
| chr1:119088273
|
C | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0333a0006c0009t0003g0326 | 4 | NA18612.hp1 NA18968.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-11666G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088273 | ||||||
| chr1:119088435
|
A | AAC | 78 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0036others(75): Show | 80 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.91-11830_91-11829d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | AACAC | 14 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0079others(11): Show | 15 | HG00423.hp1 HG00642.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-11832_91-11829d others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | AACACAC | 48 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0034others(45): Show | 49 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.91-11834_91-11829d others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | AACACACA others(1): Show |
13 | a0001c0001t0001g0031a0001c0001t0001g0065a0001c0001t0001g0072others(10): Show | 14 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.91-11836_91-11829d others(10): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | AACACACA others(3): Show |
19 | a0001c0001t0004g0022a0001c0001t0004g0024a0001c0001t0004g0030others(16): Show | 19 | HG00558.hp1 HG00609.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.91-11838_91-11829d others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | AACACACA others(5): Show |
5 | a0001c0001t0004g0023a0002c0002t0002g0001a0002c0002t0002g0132others(2): Show | 7 | HG01257.hp2 HG01258.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.91-11840_91-11829d others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | AACACACA others(7): Show |
15 | a0001c0001t0001g0141a0001c0001t0006g0158a0001c0001t0006g0161others(12): Show | 16 | HG02056.hp2 HG02129.hp1 NA18949.hp1 others(13): Show |
intron_variant | MODIFIER | c.91-11842_91-11829d others(16): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | AACACACA others(9): Show |
3 | a0001c0001t0006g0160a0002c0002t0002g0121a0002c0002t0002g0200 | 3 | HG02027.hp2 NA18940.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.91-11844_91-11829d others(18): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | AACACACA others(11): Show |
3 | a0002c0002t0002g0119a0002c0002t0002g0120a0002c0002t0002g0127 | 3 | NA18968.hp1 NA18988.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.91-11846_91-11829d others(20): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | AACACACA others(13): Show |
4 | a0002c0002t0002g0124a0002c0002t0002g0128a0002c0002t0002g0134others(1): Show | 4 | NA18939.hp2 NA18978.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-11848_91-11829d others(22): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0004g0173 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.91-11829_91-11828i others(13): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0006g0159 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.91-11829_91-11828i others(17): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
AAC | A | 17 | a0001c0001t0003g0232a0001c0001t0003g0235a0001c0003t0007g0218others(14): Show | 17 | HG00735.hp2 HG00741.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.91-11830_91-11829d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088435
|
AACACACA others(5): Show |
A | 49 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(46): Show | 53 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.91-11840_91-11829d others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088435 | ||||||
| chr1:119088468
|
A | ACACACAC others(10): Show |
1 | a0002c0002t0002g0140 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.91-11862_91-11861i others(19): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088468 | ||||||
| chr1:119088551
|
T | C | 95 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(92): Show | 99 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.91-11944A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088551 | ||||||
| chr1:119088652
|
T | C | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.91-12045A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088652 | ||||||
| chr1:119088679
|
G | T | 10 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-12072C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119088679 | ||||||
| chr1:119089175
|
C | T | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-12568G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089175 | ||||||
| chr1:119089465
|
C | T | 4 | a0001c0001t0006g0158a0001c0001t0006g0159a0001c0001t0006g0160others(1): Show | 4 | HG02056.hp2 HG02071.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-12858G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089465 | ||||||
| chr1:119089541
|
A | T | 1 | a0001c0003t0007g0218 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.91-12934T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089541 | ||||||
| chr1:119089561
|
C | T | 1 | a0001c0001t0004g0339 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.91-12954G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089561 | ||||||
| chr1:119089761
|
C | T | 3 | a0001c0001t0003g0092a0001c0001t0003g0106a0001c0001t0007g0055 | 3 | HG00099.hp1 HG01123.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.91-13154G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089761 | ||||||
| chr1:119089876
|
C | A | 1 | a0001c0001t0004g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91-13269G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089876 | ||||||
| chr1:119089911
|
T | C | 5 | a0001c0001t0003g0009a0001c0001t0003g0240a0001c0001t0003g0241others(2): Show | 6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-13304A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089911 | ||||||
| chr1:119089935
|
T | G | 1 | a0002c0002t0002g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.91-13328A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119089935 | ||||||
| chr1:119090064
|
T | C | 2 | a0001c0001t0007g0204a0001c0001t0007g0208 | 2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.91-13457A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090064 | ||||||
| chr1:119090129
|
G | GA | 8 | a0001c0001t0001g0066a0001c0001t0006g0010a0001c0001t0006g0308others(5): Show | 9 | HG00738.hp2 HG01070.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.91-13523dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090129 | ||||||
| chr1:119090129
|
GA | G | 18 | a0001c0001t0005g0210a0001c0003t0007g0218a0001c0003t0007g0219others(15): Show | 18 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.91-13523delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090129 | ||||||
| chr1:119090192
|
T | C | 61 | a0001c0001t0001g0141a0001c0001t0004g0168a0001c0001t0006g0158others(58): Show | 67 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(64): Show |
intron_variant | MODIFIER | c.91-13585A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090192 | ||||||
| chr1:119090232
|
C | T | 4 | a0001c0001t0003g0009a0001c0001t0003g0240a0001c0001t0003g0241others(1): Show | 5 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-13625G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090232 | ||||||
| chr1:119090344
|
T | G | 4 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-13737A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090344 | ||||||
| chr1:119090360
|
C | T | 1 | a0001c0001t0004g0037 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.91-13753G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090360 | ||||||
| chr1:119090919
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.91-14312G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090919 | ||||||
| chr1:119090924
|
T | C | 101 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(98): Show | 105 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.91-14317A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119090924 | ||||||
| chr1:119091088
|
A | G | 1 | a0002c0002t0011g0129 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91-14481T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091088 | ||||||
| chr1:119091356
|
G | T | 1 | a0001c0001t0016g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.91-14749C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091356 | ||||||
| chr1:119091451
|
T | C | 1 | a0002c0002t0002g0006 | 2 | HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.91-14844A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091451 | ||||||
| chr1:119091588
|
C | G | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-14981G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091588 | ||||||
| chr1:119091601
|
C | T | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.91-14994G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091601 | ||||||
| chr1:119091738
|
G | A | 5 | a0001c0003t0009g0021a0001c0003t0009g0223a0001c0003t0009g0224others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-15131C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091738 | ||||||
| chr1:119091829
|
C | T | 1 | a0001c0001t0007g0204 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.91-15222G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091829 | ||||||
| chr1:119091889
|
T | C | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.91-15282A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091889 | ||||||
| chr1:119091951
|
C | T | 1 | a0001c0001t0004g0317 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.91-15344G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119091951 | ||||||
| chr1:119092046
|
G | C | 1 | a0001c0001t0001g0029 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.91-15439C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119092046 | ||||||
| chr1:119092243
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0111 | 2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.91-15636C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119092243 | ||||||
| chr1:119092604
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.91-15997G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119092604 | ||||||
| chr1:119092655
|
C | T | 1 | a0001c0001t0005g0156 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.91-16048G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119092655 | ||||||
| chr1:119093100
|
T | C | 92 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(89): Show | 96 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.91-16493A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093100 | ||||||
| chr1:119093110
|
A | T | 100 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(97): Show | 104 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.91-16503T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093110 | ||||||
| chr1:119093184
|
T | C | 1 | a0002c0002t0002g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.91-16577A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093184 | ||||||
| chr1:119093328
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0103 | 2 | NA18948.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.91-16721A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093328 | ||||||
| chr1:119093470
|
A | G | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(287): Show | 303 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.91-16863T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093470 | ||||||
| chr1:119093474
|
A | ATACTAGA others(13): Show |
290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(287): Show | 303 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.91-16868_91-16867i others(22): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093474 | ||||||
| chr1:119093918
|
A | C | 164 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(161): Show | 174 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.91-17311T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093918 | ||||||
| chr1:119093998
|
T | C | 2 | a0001c0001t0003g0258a0001c0001t0003g0259 | 2 | NA18942.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.91-17391A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119093998 | ||||||
| chr1:119094055
|
A | G | 3 | a0001c0001t0003g0092a0001c0001t0003g0106a0001c0001t0007g0055 | 3 | HG00099.hp1 HG01123.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.91-17448T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094055 | ||||||
| chr1:119094113
|
G | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-17506C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094113 | ||||||
| chr1:119094302
|
T | G | 1 | a0001c0001t0001g0067 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.91-17695A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094302 | ||||||
| chr1:119094373
|
CT | C | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-17767delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094373 | ||||||
| chr1:119094511
|
T | G | 61 | a0001c0001t0001g0141a0001c0001t0004g0168a0001c0001t0006g0158others(58): Show | 67 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(64): Show |
intron_variant | MODIFIER | c.91-17904A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094511 | ||||||
| chr1:119094781
|
G | C | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-18174C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094781 | ||||||
| chr1:119094863
|
C | T | 1 | a0002c0002t0002g0187 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.91-18256G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119094863 | ||||||
| chr1:119095095
|
G | A | 1 | a0002c0002t0002g0192 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.91-18488C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095095 | ||||||
| chr1:119095268
|
G | A | 61 | a0001c0001t0001g0141a0001c0001t0004g0168a0001c0001t0006g0158others(58): Show | 67 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(64): Show |
intron_variant | MODIFIER | c.91-18661C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095268 | ||||||
| chr1:119095461
|
T | G | 1 | a0002c0002t0002g0121 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.91-18854A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095461 | ||||||
| chr1:119095484
|
C | T | 92 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(89): Show | 96 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.91-18877G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095484 | ||||||
| chr1:119095577
|
C | T | 23 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(20): Show | 25 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.91-18970G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095577 | ||||||
| chr1:119095763
|
G | A | 17 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(14): Show | 17 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.91-19156C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095763 | ||||||
| chr1:119095930
|
G | A | 88 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(85): Show | 92 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.91-19323C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095930 | ||||||
| chr1:119095941
|
T | C | 1 | a0003c0004t0005g0307 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.91-19334A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095941 | ||||||
| chr1:119095958
|
AC | A | 96 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(93): Show | 100 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.91-19352delG | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119095958 | ||||||
| chr1:119096232
|
T | C | 92 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(89): Show | 96 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.91-19625A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096232 | ||||||
| chr1:119096402
|
C | T | 1 | a0003c0004t0005g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.91-19795G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096402 | ||||||
| chr1:119096410
|
T | C | 4 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(1): Show | 4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-19803A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096410 | ||||||
| chr1:119096421
|
C | T | 15 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(12): Show | 15 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-19814G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096421 | ||||||
| chr1:119096470
|
T | A | 1 | a0003c0004t0005g0213 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.91-19863A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096470 | ||||||
| chr1:119096529
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.91-19922A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096529 | ||||||
| chr1:119096699
|
T | C | 1 | a0001c0003t0007g0221 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.91-20092A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096699 | ||||||
| chr1:119096935
|
C | T | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-20328G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119096935 | ||||||
| chr1:119097052
|
T | C | 99 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(96): Show | 103 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.91-20445A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097052 | ||||||
| chr1:119097068
|
G | T | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-20461C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097068 | ||||||
| chr1:119097270
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91-20663G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097270 | ||||||
| chr1:119097376
|
G | T | 1 | a0002c0002t0002g0127 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.91-20769C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097376 | ||||||
| chr1:119097464
|
A | C | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(336): Show | 353 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.91-20857T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097464 | ||||||
| chr1:119097496
|
G | A | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-20889C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097496 | ||||||
| chr1:119097551
|
C | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0115 | 2 | HG01261.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.91-20944G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097551 | ||||||
| chr1:119097716
|
G | A | 61 | a0001c0001t0001g0141a0001c0001t0004g0168a0001c0001t0006g0158others(58): Show | 67 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(64): Show |
intron_variant | MODIFIER | c.91-21109C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097716 | ||||||
| chr1:119097773
|
C | T | 1 | a0001c0001t0003g0302 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.91-21166G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097773 | ||||||
| chr1:119097778
|
C | G | 164 | a0001c0001t0001g0141a0001c0001t0001g0313a0001c0001t0001g0323others(161): Show | 174 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.91-21171G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119097778 | ||||||
| chr1:119098105
|
C | T | 88 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(85): Show | 92 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.91-21498G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098105 | ||||||
| chr1:119098202
|
T | A | 10 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-21595A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098202 | ||||||
| chr1:119098204
|
G | A | 2 | a0001c0001t0004g0017a0001c0001t0004g0018 | 2 | HG01433.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-21597C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098204 | ||||||
| chr1:119098227
|
C | G | 1 | a0002c0002t0002g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.91-21620G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098227 | ||||||
| chr1:119098362
|
C | T | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-21755G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098362 | ||||||
| chr1:119098488
|
A | G | 1 | a0002c0002t0002g0193 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.91-21881T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098488 | ||||||
| chr1:119098576
|
T | C | 7 | a0002c0002t0002g0120a0002c0002t0002g0121a0002c0002t0002g0124others(4): Show | 7 | NA18939.hp2 NA18940.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.91-21969A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098576 | ||||||
| chr1:119098582
|
C | T | 1 | a0001c0001t0007g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91-21975G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098582 | ||||||
| chr1:119098862
|
G | A | 1 | a0002c0002t0002g0191 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.91-22255C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098862 | ||||||
| chr1:119098997
|
A | G | 95 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(92): Show | 99 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.91-22390T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119098997 | ||||||
| chr1:119099033
|
G | A | 1 | a0001c0001t0007g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91-22426C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099033 | ||||||
| chr1:119099208
|
C | T | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-22601G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099208 | ||||||
| chr1:119099399
|
T | C | 25 | a0001c0001t0007g0201a0001c0001t0007g0203a0001c0001t0007g0204others(22): Show | 25 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.91-22792A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099399 | ||||||
| chr1:119099567
|
C | T | 8 | a0002c0002t0002g0132a0002c0002t0002g0135a0002c0002t0002g0136others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.91-22960G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099567 | ||||||
| chr1:119099673
|
T | C | 49 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(46): Show | 53 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.91-23066A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099673 | ||||||
| chr1:119099743
|
G | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-23136C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099743 | ||||||
| chr1:119099938
|
A | G | 5 | a0001c0001t0004g0286a0001c0001t0004g0290a0001c0001t0004g0291others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-23331T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119099938 | ||||||
| chr1:119100084
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.91-23477T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100084 | ||||||
| chr1:119100119
|
CA | C | 15 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(12): Show | 15 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-23513delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100119 | ||||||
| chr1:119100158
|
T | C | 9 | a0001c0001t0003g0250a0001c0001t0003g0253a0001c0001t0003g0255others(6): Show | 9 | HG00438.hp2 HG02071.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.91-23551A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100158 | ||||||
| chr1:119100162
|
T | G | 2 | a0001c0001t0006g0318a0001c0001t0006g0332 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.91-23555A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100162 | ||||||
| chr1:119100272
|
CAGAAAAG others(2): Show |
C | 3 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0010t0004g0287 | 3 | HG01891.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.91-23674_91-23666d others(11): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100272 | ||||||
| chr1:119100328
|
A | G | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-23721T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100328 | ||||||
| chr1:119100356
|
T | C | 9 | a0001c0001t0004g0011a0001c0001t0004g0012a0001c0001t0004g0317others(6): Show | 11 | HG01884.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.91-23749A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100356 | ||||||
| chr1:119100491
|
G | C | 1 | a0001c0003t0007g0218 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.91-23884C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100491 | ||||||
| chr1:119100573
|
A | T | 2 | a0001c0001t0006g0321a0001c0001t0006g0322 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.91-23966T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100573 | ||||||
| chr1:119100730
|
G | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-24123C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100730 | ||||||
| chr1:119100765
|
A | AT | 4 | a0002c0002t0002g0121a0002c0002t0002g0124a0002c0002t0002g0128others(1): Show | 4 | NA18939.hp2 NA18940.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-24159dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100765 | ||||||
| chr1:119100822
|
G | A | 1 | a0001c0001t0007g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91-24215C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100822 | ||||||
| chr1:119100886
|
C | G | 11 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(8): Show | 11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.91-24279G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100886 | ||||||
| chr1:119100901
|
G | T | 1 | a0002c0002t0002g0196 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.91-24294C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100901 | ||||||
| chr1:119100923
|
C | A | 54 | a0001c0001t0001g0141a0001c0001t0004g0168a0001c0001t0006g0158others(51): Show | 60 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(57): Show |
intron_variant | MODIFIER | c.91-24316G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100923 | ||||||
| chr1:119100928
|
G | A | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-24321C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100928 | ||||||
| chr1:119100997
|
C | T | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-24390G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119100997 | ||||||
| chr1:119101074
|
G | A | 1 | a0002c0002t0011g0130 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.91-24467C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119101074 | ||||||
| chr1:119101151
|
A | G | 63 | a0001c0001t0001g0067a0001c0001t0001g0141a0001c0001t0004g0017others(60): Show | 69 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(66): Show |
intron_variant | MODIFIER | c.91-24544T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119101151 | ||||||
| chr1:119101197
|
T | C | 54 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(51): Show | 58 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.91-24590A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119101197 | ||||||
| chr1:119101285
|
C | G | 1 | a0001c0001t0004g0325 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91-24678G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119101285 | ||||||
| chr1:119101643
|
A | G | 1 | a0001c0001t0004g0339 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.91-25036T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119101643 | ||||||
| chr1:119102070
|
T | TG | 13 | a0001c0001t0001g0066a0001c0001t0001g0089a0001c0001t0001g0178others(10): Show | 13 | HG01175.hp2 HG01433.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.91-25464dupC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102070 | ||||||
| chr1:119102111
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.91-25504T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102111 | ||||||
| chr1:119102376
|
AC | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-25770delG | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102376 | ||||||
| chr1:119102483
|
C | T | 5 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(2): Show | 5 | HG00408.hp1 HG01099.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-25876G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102483 | ||||||
| chr1:119102543
|
T | C | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.91-25936A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102543 | ||||||
| chr1:119102859
|
G | T | 1 | a0001c0001t0004g0017 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.91-26252C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102859 | ||||||
| chr1:119102912
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(179): Show | 190 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.91-26305G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102912 | ||||||
| chr1:119102918
|
T | C | 4 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(1): Show | 4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-26311A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119102918 | ||||||
| chr1:119103072
|
A | G | 1 | a0001c0001t0007g0203 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.91-26465T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103072 | ||||||
| chr1:119103234
|
T | C | 1 | a0001c0001t0003g0269 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.91-26627A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103234 | ||||||
| chr1:119103278
|
C | T | 4 | a0001c0003t0007g0289a0001c0003t0007g0295a0001c0003t0007g0296others(1): Show | 4 | HG02735.hp2 HG03239.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-26671G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103278 | ||||||
| chr1:119103395
|
G | C | 4 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0001t0004g0293others(1): Show | 4 | HG02486.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-26788C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103395 | ||||||
| chr1:119103412
|
T | C | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(287): Show | 303 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.91-26805A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103412 | ||||||
| chr1:119103449
|
G | A | 1 | a0001c0003t0007g0254 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91-26842C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103449 | ||||||
| chr1:119103474
|
T | C | 1 | a0001c0001t0005g0146 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.91-26867A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103474 | ||||||
| chr1:119103623
|
T | A | 1 | a0002c0002t0002g0128 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.91-27016A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103623 | ||||||
| chr1:119103834
|
G | A | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91-27227C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103834 | ||||||
| chr1:119103971
|
T | C | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-27364A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119103971 | ||||||
| chr1:119104071
|
A | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(271): Show | 286 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.91-27464T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104071 | ||||||
| chr1:119104075
|
G | A | 1 | a0001c0003t0007g0298 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.91-27468C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104075 | ||||||
| chr1:119104253
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.91-27646G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104253 | ||||||
| chr1:119104437
|
C | T | 3 | a0001c0001t0008g0280a0001c0001t0008g0282a0001c0001t0008g0340 | 3 | HG03225.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.91-27830G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104437 | ||||||
| chr1:119104621
|
G | GA | 9 | a0001c0001t0001g0036a0001c0001t0003g0009a0001c0001t0003g0240others(6): Show | 10 | HG01168.hp1 HG02040.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-28015dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104621 | ||||||
| chr1:119104621
|
GA | G | 33 | a0001c0001t0001g0178a0001c0001t0003g0302a0001c0001t0004g0286others(30): Show | 33 | HG01891.hp1 HG02027.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.91-28015delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104621 | ||||||
| chr1:119104621
|
GAA | G | 36 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(33): Show | 40 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.91-28016_91-28015d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104621 | ||||||
| chr1:119104625
|
A | T | 1 | a0002c0002t0002g0180 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.91-28018T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104625 | ||||||
| chr1:119104765
|
C | CA | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(101): Show | 106 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.91-28159dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104765 | ||||||
| chr1:119104887
|
T | A | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91-28280A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119104887 | ||||||
| chr1:119105019
|
G | C | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-28412C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105019 | ||||||
| chr1:119105181
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(3): Show | 6 | HG00621.hp2 HG00673.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-28574C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105181 | ||||||
| chr1:119105323
|
C | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(179): Show | 190 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.91-28716G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105323 | ||||||
| chr1:119105503
|
G | A | 1 | a0001c0001t0006g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.91-28896C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105503 | ||||||
| chr1:119105686
|
C | T | 59 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(56): Show | 63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.91-29079G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105686 | ||||||
| chr1:119105859
|
G | A | 1 | a0001c0001t0003g0232 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.91-29252C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105859 | ||||||
| chr1:119105915
|
AATAAAAG others(5): Show |
A | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.91-29320_91-29309d others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119105915 | ||||||
| chr1:119106033
|
T | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(191): Show | 202 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.91-29426A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106033 | ||||||
| chr1:119106165
|
T | C | 1 | a0001c0001t0003g0249 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.91-29558A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106165 | ||||||
| chr1:119106224
|
C | CCT | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(195): Show | 206 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.91-29619_91-29618d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106224 | ||||||
| chr1:119106647
|
C | A | 1 | a0001c0001t0016g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.91-30040G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106647 | ||||||
| chr1:119106854
|
G | A | 1 | a0001c0001t0012g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.91-30247C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106854 | ||||||
| chr1:119106882
|
C | T | 1 | a0001c0001t0004g0301 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.91-30275G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106882 | ||||||
| chr1:119106926
|
T | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-30319A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119106926 | ||||||
| chr1:119107145
|
T | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-30538A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107145 | ||||||
| chr1:119107359
|
C | G | 1 | a0002c0002t0002g0076 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.91-30752G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107359 | ||||||
| chr1:119107438
|
TTTTGA | T | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-30836_91-30832d others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107438 | ||||||
| chr1:119107571
|
T | A | 1 | a0001c0001t0005g0157 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.91-30964A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107571 | ||||||
| chr1:119107661
|
TAGAAAA | T | 5 | a0001c0001t0003g0009a0001c0001t0003g0240a0001c0001t0003g0241others(2): Show | 6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-31060_91-31055d others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107661 | ||||||
| chr1:119107671
|
AAGAG | A | 59 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(56): Show | 63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.91-31068_91-31065d others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107671 | ||||||
| chr1:119107671
|
AAGAGAG | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-31070_91-31065d others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107671 | ||||||
| chr1:119107671
|
AAGAGAGA others(7): Show |
A | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(191): Show | 202 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.91-31078_91-31065d others(16): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107671 | ||||||
| chr1:119107697
|
G | GA | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-31091dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107697 | ||||||
| chr1:119107738
|
G | A | 1 | a0001c0001t0003g0259 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.91-31131C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107738 | ||||||
| chr1:119107975
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0108 | 2 | HG01243.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.91-31368C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119107975 | ||||||
| chr1:119108002
|
C | G | 1 | a0001c0003t0007g0296 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.91-31395G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108002 | ||||||
| chr1:119108072
|
A | G | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.91-31465T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108072 | ||||||
| chr1:119108172
|
T | G | 59 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(56): Show | 63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.91-31565A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108172 | ||||||
| chr1:119108305
|
A | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(175): Show | 186 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.91-31698T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108305 | ||||||
| chr1:119108308
|
A | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(183): Show | 194 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.91-31701T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108308 | ||||||
| chr1:119108370
|
T | G | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-31763A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108370 | ||||||
| chr1:119108468
|
G | A | 1 | a0001c0001t0004g0325 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91-31861C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108468 | ||||||
| chr1:119108469
|
C | T | 1 | a0001c0001t0004g0325 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91-31862G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108469 | ||||||
| chr1:119108544
|
TTATGA | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(175): Show | 186 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.91-31942_91-31938d others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108544 | ||||||
| chr1:119108585
|
C | T | 1 | a0002c0002t0002g0140 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.90+31970G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108585 | ||||||
| chr1:119108745
|
C | A | 2 | a0001c0003t0007g0221a0001c0003t0007g0222 | 2 | HG00741.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.90+31810G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108745 | ||||||
| chr1:119108785
|
T | C | 3 | a0001c0001t0003g0033a0001c0001t0003g0056a0001c0001t0003g0094 | 3 | HG01243.hp1 HG02004.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.90+31770A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108785 | ||||||
| chr1:119108820
|
T | C | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+31735A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119108820 | ||||||
| chr1:119109264
|
C | A | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+31291G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109264 | ||||||
| chr1:119109278
|
G | C | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+31277C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109278 | ||||||
| chr1:119109402
|
A | G | 1 | a0002c0002t0002g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.90+31153T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109402 | ||||||
| chr1:119109432
|
A | G | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+31123T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109432 | ||||||
| chr1:119109504
|
G | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+31051C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109504 | ||||||
| chr1:119109845
|
A | T | 1 | a0002c0002t0002g0181 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.90+30710T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109845 | ||||||
| chr1:119109978
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(79): Show | 84 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.90+30577G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119109978 | ||||||
| chr1:119110245
|
G | C | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+30310C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119110245 | ||||||
| chr1:119110308
|
C | T | 4 | a0001c0001t0006g0158a0001c0001t0006g0159a0001c0001t0006g0160others(1): Show | 4 | HG02056.hp2 HG02071.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+30247G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119110308 | ||||||
| chr1:119110459
|
T | C | 1 | a0001c0001t0003g0217 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.90+30096A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119110459 | ||||||
| chr1:119110627
|
C | T | 1 | a0001c0001t0006g0319 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.90+29928G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119110627 | ||||||
| chr1:119110737
|
T | C | 1 | a0001c0001t0012g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.90+29818A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119110737 | ||||||
| chr1:119111142
|
AG | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG00558.hp1 NA18981.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+29412delC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119111142 | ||||||
| chr1:119111277
|
T | C | 2 | a0001c0001t0004g0017a0001c0001t0004g0018 | 2 | HG01433.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+29278A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119111277 | ||||||
| chr1:119111787
|
C | T | 5 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(2): Show | 5 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+28768G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119111787 | ||||||
| chr1:119111847
|
T | C | 1 | a0001c0001t0006g0331 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.90+28708A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119111847 | ||||||
| chr1:119111865
|
C | T | 4 | a0001c0001t0004g0290a0001c0001t0004g0291a0001c0001t0004g0293others(1): Show | 4 | HG02486.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+28690G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119111865 | ||||||
| chr1:119112092
|
T | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+28463A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112092 | ||||||
| chr1:119112207
|
C | G | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+28348G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112207 | ||||||
| chr1:119112326
|
G | A | 1 | a0001c0001t0005g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.90+28229C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112326 | ||||||
| chr1:119112353
|
T | C | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+28202A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112353 | ||||||
| chr1:119112363
|
A | C | 1 | a0001c0001t0001g0324 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.90+28192T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112363 | ||||||
| chr1:119112436
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90+28119G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112436 | ||||||
| chr1:119112504
|
T | C | 6 | a0001c0001t0003g0302a0001c0001t0004g0301a0001c0001t0010g0292others(3): Show | 6 | HG02818.hp2 HG03098.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+28051A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112504 | ||||||
| chr1:119112939
|
T | A | 10 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(7): Show | 10 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+27616A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112939 | ||||||
| chr1:119112989
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.90+27566C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119112989 | ||||||
| chr1:119113056
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.90+27499T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113056 | ||||||
| chr1:119113057
|
T | C | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(282): Show | 297 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.90+27498A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113057 | ||||||
| chr1:119113098
|
G | T | 1 | a0001c0001t0001g0079 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.90+27457C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113098 | ||||||
| chr1:119113274
|
A | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(195): Show | 206 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.90+27281T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113274 | ||||||
| chr1:119113350
|
T | C | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+27205A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113350 | ||||||
| chr1:119113732
|
T | A | 2 | a0002c0002t0002g0122a0002c0002t0002g0126 | 2 | HG02129.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.90+26823A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113732 | ||||||
| chr1:119113783
|
T | C | 8 | a0002c0002t0002g0132a0002c0002t0002g0135a0002c0002t0002g0136others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.90+26772A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113783 | ||||||
| chr1:119113870
|
T | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(195): Show | 206 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.90+26685A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119113870 | ||||||
| chr1:119114244
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(242): Show | 257 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.90+26311C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114244 | ||||||
| chr1:119114272
|
C | T | 1 | a0001c0001t0003g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.90+26283G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114272 | ||||||
| chr1:119114434
|
T | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(195): Show | 206 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.90+26121A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114434 | ||||||
| chr1:119114471
|
A | T | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+26084T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114471 | ||||||
| chr1:119114585
|
G | C | 1 | a0001c0001t0001g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.90+25970C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114585 | ||||||
| chr1:119114616
|
A | G | 1 | a0001c0001t0003g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.90+25939T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114616 | ||||||
| chr1:119114762
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.90+25793G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114762 | ||||||
| chr1:119114809
|
C | T | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+25746G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119114809 | ||||||
| chr1:119115029
|
A | C | 1 | a0001c0001t0007g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.90+25526T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115029 | ||||||
| chr1:119115097
|
C | A | 5 | a0002c0002t0002g0004a0002c0002t0002g0125a0002c0002t0002g0133others(2): Show | 6 | HG01175.hp1 HG02630.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+25458G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115097 | ||||||
| chr1:119115120
|
T | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(175): Show | 186 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.90+25435A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115120 | ||||||
| chr1:119115304
|
G | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | NA18995.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.90+25251C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115304 | ||||||
| chr1:119115315
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(98): Show | 103 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.90+25240A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115315 | ||||||
| chr1:119115462
|
C | T | 1 | a0002c0002t0002g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.90+25093G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115462 | ||||||
| chr1:119115726
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0044others(1): Show | 4 | HG00673.hp2 NA18612.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+24829T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115726 | ||||||
| chr1:119115794
|
C | T | 1 | a0001c0003t0007g0289 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.90+24761G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119115794 | ||||||
| chr1:119116301
|
C | T | 2 | a0001c0006t0004g0025a0001c0006t0004g0175 | 2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.90+24254G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116301 | ||||||
| chr1:119116302
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(183): Show | 194 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.90+24253T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116302 | ||||||
| chr1:119116464
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0091others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+24091C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116464 | ||||||
| chr1:119116564
|
C | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0078 | 2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.90+23991G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116564 | ||||||
| chr1:119116748
|
G | A | 10 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(7): Show | 10 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+23807C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116748 | ||||||
| chr1:119116752
|
A | C | 14 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(11): Show | 14 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+23803T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116752 | ||||||
| chr1:119116778
|
G | T | 3 | a0002c0002t0002g0001a0002c0002t0002g0118a0002c0002t0002g0138 | 5 | HG01257.hp2 HG01258.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+23777C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116778 | ||||||
| chr1:119116796
|
C | T | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(191): Show | 202 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.90+23759G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116796 | ||||||
| chr1:119116974
|
G | A | 5 | a0001c0001t0004g0286a0001c0001t0004g0290a0001c0001t0004g0291others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+23581C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116974 | ||||||
| chr1:119116984
|
A | T | 3 | a0001c0001t0003g0008a0001c0001t0003g0229a0001c0001t0003g0230 | 4 | NA19001.hp1 NA19004.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+23571T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116984 | ||||||
| chr1:119116993
|
C | A | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+23562G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119116993 | ||||||
| chr1:119117060
|
C | T | 4 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+23495G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117060 | ||||||
| chr1:119117149
|
T | C | 14 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(11): Show | 14 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+23406A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117149 | ||||||
| chr1:119117226
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(256): Show | 271 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.90+23329T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117226 | ||||||
| chr1:119117295
|
G | A | 1 | a0001c0001t0016g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.90+23260C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117295 | ||||||
| chr1:119117369
|
T | C | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+23186A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117369 | ||||||
| chr1:119117653
|
C | T | 8 | a0001c0001t0004g0011a0001c0001t0004g0335a0001c0001t0004g0336others(5): Show | 9 | HG00408.hp1 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.90+22902G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117653 | ||||||
| chr1:119117683
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0108 | 3 | HG01243.hp2 HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.90+22872G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117683 | ||||||
| chr1:119117831
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.90+22724G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117831 | ||||||
| chr1:119117882
|
G | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(175): Show | 186 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.90+22673C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117882 | ||||||
| chr1:119117978
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.90+22577C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119117978 | ||||||
| chr1:119118153
|
T | C | 3 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213 | 3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.90+22402A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118153 | ||||||
| chr1:119118196
|
G | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(179): Show | 190 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.90+22359C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118196 | ||||||
| chr1:119118294
|
G | T | 5 | a0001c0001t0003g0231a0001c0001t0003g0232a0001c0001t0003g0233others(2): Show | 5 | HG00735.hp2 HG00741.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+22261C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118294 | ||||||
| chr1:119118440
|
G | A | 1 | a0001c0001t0003g0107 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.90+22115C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118440 | ||||||
| chr1:119118581
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0108 | 3 | HG01243.hp2 HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.90+21974G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118581 | ||||||
| chr1:119118669
|
A | G | 1 | a0001c0001t0016g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.90+21886T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118669 | ||||||
| chr1:119118898
|
C | A | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(282): Show | 297 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(294): Show |
intron_variant | MODIFIER | c.90+21657G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118898 | ||||||
| chr1:119118954
|
C | A | 1 | a0001c0001t0005g0156 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.90+21601G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119118954 | ||||||
| chr1:119119134
|
A | C | 10 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+21421T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119134 | ||||||
| chr1:119119393
|
C | T | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+21162G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119393 | ||||||
| chr1:119119648
|
C | T | 7 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0041others(4): Show | 7 | HG02129.hp2 NA18964.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+20907G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119648 | ||||||
| chr1:119119654
|
A | C | 1 | a0001c0001t0004g0172 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.90+20901T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119654 | ||||||
| chr1:119119699
|
A | G | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+20856T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119699 | ||||||
| chr1:119119760
|
C | T | 1 | a0002c0002t0002g0076 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.90+20795G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119760 | ||||||
| chr1:119119859
|
T | A | 12 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(9): Show | 12 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.90+20696A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119119859 | ||||||
| chr1:119120176
|
A | G | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(98): Show | 103 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.90+20379T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120176 | ||||||
| chr1:119120331
|
C | T | 2 | a0003c0004t0005g0212a0003c0004t0005g0213 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.90+20224G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120331 | ||||||
| chr1:119120461
|
T | C | 2 | a0002c0002t0002g0143a0002c0002t0002g0144 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.90+20094A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120461 | ||||||
| chr1:119120529
|
A | G | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.90+20026T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120529 | ||||||
| chr1:119120755
|
G | A | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+19800C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120755 | ||||||
| chr1:119120798
|
T | C | 1 | a0002c0002t0002g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.90+19757A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120798 | ||||||
| chr1:119120927
|
C | T | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+19628G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119120927 | ||||||
| chr1:119121090
|
C | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(195): Show | 206 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.90+19465G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121090 | ||||||
| chr1:119121192
|
A | G | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.90+19363T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121192 | ||||||
| chr1:119121445
|
A | T | 1 | a0001c0001t0003g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90+19110T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121445 | ||||||
| chr1:119121625
|
T | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(191): Show | 202 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.90+18930A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121625 | ||||||
| chr1:119121640
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.90+18915G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121640 | ||||||
| chr1:119121697
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.90+18858C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121697 | ||||||
| chr1:119121813
|
A | G | 1 | a0003c0004t0005g0307 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+18742T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119121813 | ||||||
| chr1:119122296
|
T | A | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+18259A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122296 | ||||||
| chr1:119122335
|
A | G | 1 | a0002c0002t0002g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.90+18220T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122335 | ||||||
| chr1:119122339
|
T | C | 1 | a0001c0001t0004g0037 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.90+18216A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122339 | ||||||
| chr1:119122441
|
G | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0105 | 2 | NA19070.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.90+18114C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122441 | ||||||
| chr1:119122469
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.90+18086A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122469 | ||||||
| chr1:119122506
|
T | G | 40 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0004g0194others(37): Show | 45 | HG00423.hp2 HG01257.hp2 HG01258.hp1 others(42): Show |
intron_variant | MODIFIER | c.90+18049A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122506 | ||||||
| chr1:119122711
|
A | G | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+17844T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122711 | ||||||
| chr1:119122770
|
A | T | 1 | a0002c0002t0002g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.90+17785T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122770 | ||||||
| chr1:119122899
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0091others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+17656C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119122899 | ||||||
| chr1:119123039
|
G | A | 1 | a0001c0010t0004g0287 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.90+17516C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123039 | ||||||
| chr1:119123240
|
C | T | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(198): Show | 209 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.90+17315G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123240 | ||||||
| chr1:119123336
|
A | G | 1 | a0001c0007t0004g0014 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.90+17219T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123336 | ||||||
| chr1:119123570
|
CTG | C | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+16983_90+16984d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123570 | ||||||
| chr1:119123603
|
A | AAC | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(153): Show | 164 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.90+16950_90+16951d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123603 | ||||||
| chr1:119123603
|
AAC | A | 39 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(36): Show | 39 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.90+16950_90+16951d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123603 | ||||||
| chr1:119123669
|
T | A | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16886A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123669 | ||||||
| chr1:119123674
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16881G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123674 | ||||||
| chr1:119123675
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16880G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123675 | ||||||
| chr1:119123685
|
T | A | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16870A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123685 | ||||||
| chr1:119123686
|
C | A | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16869G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123686 | ||||||
| chr1:119123689
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16866G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123689 | ||||||
| chr1:119123703
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16852C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123703 | ||||||
| chr1:119123704
|
A | C | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16851T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123704 | ||||||
| chr1:119123708
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16847A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123708 | ||||||
| chr1:119123710
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16845G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123710 | ||||||
| chr1:119123712
|
A | AACGTGCT others(11): Show |
1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16842_90+16843i others(20): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123712 | ||||||
| chr1:119123714
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16841G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123714 | ||||||
| chr1:119123715
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.90+16840A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123715 | ||||||
| chr1:119123870
|
G | A | 10 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+16685C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123870 | ||||||
| chr1:119123942
|
A | G | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.90+16613T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119123942 | ||||||
| chr1:119124025
|
C | A | 1 | a0001c0001t0003g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.90+16530G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124025 | ||||||
| chr1:119124144
|
T | C | 3 | a0001c0001t0004g0194a0002c0002t0002g0007a0002c0002t0002g0193 | 4 | NA18949.hp2 NA18964.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+16411A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124144 | ||||||
| chr1:119124467
|
G | A | 1 | a0001c0003t0007g0295 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.90+16088C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124467 | ||||||
| chr1:119124473
|
G | A | 1 | a0001c0001t0006g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.90+16082C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124473 | ||||||
| chr1:119124498
|
GAATGAAA others(3): Show |
G | 7 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(4): Show | 7 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+16047_90+16056d others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124498 | ||||||
| chr1:119124651
|
G | A | 1 | a0001c0001t0003g0107 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.90+15904C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124651 | ||||||
| chr1:119124655
|
C | T | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+15900G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124655 | ||||||
| chr1:119124687
|
T | C | 3 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213 | 3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.90+15868A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119124687 | ||||||
| chr1:119125146
|
A | G | 5 | a0001c0003t0007g0218a0001c0003t0007g0219a0001c0003t0007g0220others(2): Show | 5 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+15409T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119125146 | ||||||
| chr1:119125464
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0113 | 2 | HG00738.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.90+15091G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119125464 | ||||||
| chr1:119125827
|
A | C | 1 | a0002c0002t0002g0193 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.90+14728T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119125827 | ||||||
| chr1:119125828
|
G | A | 1 | a0002c0002t0002g0193 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.90+14727C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119125828 | ||||||
| chr1:119125912
|
C | G | 1 | a0001c0001t0003g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.90+14643G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119125912 | ||||||
| chr1:119126017
|
T | C | 59 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(56): Show | 63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.90+14538A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126017 | ||||||
| chr1:119126021
|
T | C | 3 | a0001c0001t0004g0194a0002c0002t0002g0007a0002c0002t0002g0193 | 4 | NA18949.hp2 NA18964.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+14534A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126021 | ||||||
| chr1:119126267
|
GA | G | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(282): Show | 297 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.90+14287delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126267 | ||||||
| chr1:119126284
|
AT | A | 5 | a0001c0001t0003g0009a0001c0001t0003g0240a0001c0001t0003g0241others(2): Show | 6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+14270delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126284 | ||||||
| chr1:119126455
|
T | C | 3 | a0003c0004t0005g0211a0003c0004t0005g0212a0003c0004t0005g0213 | 3 | HG02647.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.90+14100A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126455 | ||||||
| chr1:119126479
|
AT | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(252): Show | 265 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.90+14075delA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126479 | ||||||
| chr1:119126479
|
ATT | A | 16 | a0001c0001t0001g0065a0001c0001t0001g0112a0001c0001t0001g0215others(13): Show | 18 | HG00735.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.90+14074_90+14075d others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126479 | ||||||
| chr1:119126563
|
T | C | 2 | a0001c0001t0006g0318a0001c0001t0006g0332 | 2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.90+13992A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126563 | ||||||
| chr1:119126639
|
C | A | 55 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0004g0168others(52): Show | 61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.90+13916G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126639 | ||||||
| chr1:119126643
|
G | C | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(198): Show | 209 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.90+13912C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126643 | ||||||
| chr1:119126648
|
A | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(198): Show | 209 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.90+13907T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126648 | ||||||
| chr1:119126695
|
T | C | 13 | a0001c0001t0007g0020a0001c0003t0007g0218a0001c0003t0007g0219others(10): Show | 13 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.90+13860A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126695 | ||||||
| chr1:119126883
|
G | A | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.90+13672C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126883 | ||||||
| chr1:119126887
|
C | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0067a0001c0001t0001g0073others(3): Show | 6 | HG01261.hp1 HG01934.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+13668G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119126887 | ||||||
| chr1:119127098
|
C | A | 4 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+13457G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127098 | ||||||
| chr1:119127173
|
T | C | 9 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(6): Show | 9 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+13382A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127173 | ||||||
| chr1:119127226
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.90+13329C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127226 | ||||||
| chr1:119127270
|
G | A | 11 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(8): Show | 11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+13285C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127270 | ||||||
| chr1:119127497
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(108): Show | 113 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.90+13058T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127497 | ||||||
| chr1:119127528
|
C | T | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+13027G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127528 | ||||||
| chr1:119127572
|
A | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(205): Show | 216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.90+12983T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127572 | ||||||
| chr1:119127665
|
T | G | 6 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0005g0149others(3): Show | 6 | HG01167.hp2 HG01358.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+12890A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127665 | ||||||
| chr1:119127679
|
C | T | 10 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+12876G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127679 | ||||||
| chr1:119127823
|
T | A | 1 | a0001c0001t0007g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.90+12732A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127823 | ||||||
| chr1:119127863
|
A | G | 1 | a0001c0001t0004g0012 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.90+12692T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119127863 | ||||||
| chr1:119128070
|
A | T | 3 | a0001c0001t0001g0073a0001c0003t0007g0227a0001c0003t0007g0228 | 3 | HG03490.hp2 HG03704.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.90+12485T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128070 | ||||||
| chr1:119128114
|
G | A | 11 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(8): Show | 11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+12441C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128114 | ||||||
| chr1:119128182
|
A | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(208): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.90+12373T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128182 | ||||||
| chr1:119128199
|
C | T | 1 | a0001c0003t0007g0218 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.90+12356G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128199 | ||||||
| chr1:119128342
|
A | G | 4 | a0001c0001t0004g0011a0001c0001t0004g0335a0001c0001t0004g0336others(1): Show | 5 | HG01884.hp1 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+12213T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128342 | ||||||
| chr1:119128376
|
C | T | 7 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(4): Show | 7 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+12179G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128376 | ||||||
| chr1:119128459
|
C | T | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(201): Show | 212 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.90+12096G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128459 | ||||||
| chr1:119128486
|
C | G | 1 | a0001c0001t0003g0231 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.90+12069G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128486 | ||||||
| chr1:119128492
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.90+12063A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128492 | ||||||
| chr1:119128576
|
A | C | 1 | a0002c0002t0002g0180 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.90+11979T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128576 | ||||||
| chr1:119128594
|
C | G | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+11961G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128594 | ||||||
| chr1:119128599
|
G | A | 7 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(4): Show | 7 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+11956C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128599 | ||||||
| chr1:119128680
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.90+11875G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128680 | ||||||
| chr1:119128867
|
G | C | 1 | a0003c0004t0005g0307 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+11688C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128867 | ||||||
| chr1:119128933
|
A | G | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+11622T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119128933 | ||||||
| chr1:119129062
|
T | C | 1 | a0001c0001t0016g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.90+11493A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129062 | ||||||
| chr1:119129187
|
C | T | 5 | a0001c0003t0009g0021a0001c0003t0009g0223a0001c0003t0009g0224others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+11368G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129187 | ||||||
| chr1:119129330
|
G | A | 1 | a0001c0001t0006g0010 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.90+11225C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129330 | ||||||
| chr1:119129434
|
C | G | 1 | a0001c0001t0004g0339 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.90+11121G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129434 | ||||||
| chr1:119129478
|
G | A | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.90+11077C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129478 | ||||||
| chr1:119129727
|
T | TA | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(180): Show | 189 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.90+10827dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129727 | ||||||
| chr1:119129733
|
A | AT | 3 | a0001c0001t0001g0042a0002c0002t0002g0001a0002c0002t0002g0138 | 5 | HG01257.hp2 HG01258.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+10821_90+10822i others(3): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129733 | ||||||
| chr1:119129733
|
A | T | 13 | a0001c0001t0007g0020a0001c0003t0007g0218a0001c0003t0007g0219others(10): Show | 13 | HG00741.hp2 HG01099.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.90+10822T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129733 | ||||||
| chr1:119129738
|
T | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0108 | 2 | HG01243.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.90+10817A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129738 | ||||||
| chr1:119129800
|
A | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(200): Show | 211 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.90+10755T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129800 | ||||||
| chr1:119129919
|
T | C | 1 | a0001c0001t0012g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.90+10636A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119129919 | ||||||
| chr1:119130026
|
G | A | 16 | a0001c0001t0005g0117a0001c0001t0005g0145a0001c0001t0005g0146others(13): Show | 16 | HG00621.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+10529C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130026 | ||||||
| chr1:119130035
|
C | T | 1 | a0003c0004t0005g0307 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+10520G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130035 | ||||||
| chr1:119130143
|
GA | G | 60 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(57): Show | 64 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.90+10411delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130143 | ||||||
| chr1:119130178
|
G | A | 1 | a0001c0001t0003g0251 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.90+10377C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130178 | ||||||
| chr1:119130211
|
T | C | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+10344A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130211 | ||||||
| chr1:119130470
|
C | T | 55 | a0001c0001t0001g0141a0001c0001t0001g0178a0001c0001t0004g0168others(52): Show | 61 | HG00423.hp2 HG01175.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.90+10085G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130470 | ||||||
| chr1:119130721
|
G | A | 88 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(85): Show | 92 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.90+9834C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130721 | ||||||
| chr1:119130858
|
C | A | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(297): Show | 313 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.90+9697G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119130858 | ||||||
| chr1:119131439
|
G | A | 3 | a0001c0001t0004g0288a0001c0001t0004g0294a0001c0010t0004g0287 | 3 | HG01891.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.90+9116C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131439 | ||||||
| chr1:119131458
|
G | GT | 57 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(54): Show | 61 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.90+9096dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131458 | ||||||
| chr1:119131458
|
G | GTT | 5 | a0001c0001t0004g0305a0001c0001t0004g0336a0001c0001t0006g0309others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+9095_90+9096dup others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131458 | ||||||
| chr1:119131458
|
G | T | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+9097C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131458 | ||||||
| chr1:119131464
|
T | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(184): Show | 195 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.90+9091A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131464 | ||||||
| chr1:119131464
|
TG | T | 9 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0279others(6): Show | 9 | HG02572.hp1 HG02895.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+9090delC | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131464 | ||||||
| chr1:119131465
|
G | GT | 23 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(20): Show | 25 | HG00544.hp2 HG01952.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.90+9089dupA | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131465 | ||||||
| chr1:119131465
|
G | T | 82 | a0001c0001t0001g0038a0001c0001t0001g0313a0001c0001t0001g0323others(79): Show | 86 | HG00408.hp1 HG00438.hp1 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.90+9090C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131465 | ||||||
| chr1:119131602
|
G | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(192): Show | 203 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.90+8953C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131602 | ||||||
| chr1:119131622
|
C | T | 1 | a0001c0003t0007g0295 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.90+8933G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131622 | ||||||
| chr1:119131697
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(89): Show | 94 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.90+8858C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131697 | ||||||
| chr1:119131703
|
T | C | 1 | a0001c0003t0007g0254 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.90+8852A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131703 | ||||||
| chr1:119131707
|
C | G | 1 | a0005c0008t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.90+8848G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131707 | ||||||
| chr1:119131707
|
C | T | 1 | a0001c0001t0004g0335 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.90+8848G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131707 | ||||||
| chr1:119131708
|
G | C | 1 | a0005c0008t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.90+8847C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131708 | ||||||
| chr1:119131740
|
C | T | 7 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(4): Show | 7 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+8815G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131740 | ||||||
| chr1:119131743
|
G | A | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+8812C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131743 | ||||||
| chr1:119131795
|
TCTGGACT others(12): Show |
T | 1 | a0001c0003t0007g0254 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.90+8741_90+8759del others(19): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131795 | ||||||
| chr1:119131929
|
T | C | 6 | a0001c0001t0005g0123a0001c0001t0005g0131a0001c0001t0005g0137others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+8626A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119131929 | ||||||
| chr1:119132025
|
A | T | 59 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(56): Show | 63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.90+8530T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119132025 | ||||||
| chr1:119132299
|
T | C | 2 | a0001c0003t0007g0221a0001c0003t0007g0222 | 2 | HG00741.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.90+8256A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119132299 | ||||||
| chr1:119132560
|
T | C | 1 | a0003c0004t0005g0307 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+7995A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119132560 | ||||||
| chr1:119132673
|
G | T | 1 | a0001c0001t0003g0253 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.90+7882C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119132673 | ||||||
| chr1:119132797
|
T | C | 1 | a0003c0004t0005g0307 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+7758A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119132797 | ||||||
| chr1:119133525
|
A | G | 2 | a0001c0001t0006g0321a0001c0001t0006g0322 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.90+7030T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119133525 | ||||||
| chr1:119133665
|
C | G | 1 | a0001c0001t0001g0036 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90+6890G>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119133665 | ||||||
| chr1:119133868
|
A | C | 1 | a0001c0001t0001g0029 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.90+6687T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119133868 | ||||||
| chr1:119134064
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.90+6491G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134064 | ||||||
| chr1:119134221
|
C | A | 4 | a0001c0001t0005g0263a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG00408.hp1 NA18962.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+6334G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134221 | ||||||
| chr1:119134319
|
C | CA | 29 | a0001c0001t0003g0239a0001c0001t0003g0244a0001c0001t0003g0261others(26): Show | 29 | HG01168.hp1 HG01891.hp1 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.90+6235dupT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134319 | ||||||
| chr1:119134319
|
C | CAA | 83 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0068others(80): Show | 89 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.90+6234_90+6235dup others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134319 | ||||||
| chr1:119134319
|
C | CAAA | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(101): Show | 106 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.90+6233_90+6235dup others(3): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134319 | ||||||
| chr1:119134319
|
C | CAAAA | 27 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0062others(24): Show | 27 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.90+6232_90+6235dup others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134319 | ||||||
| chr1:119134345
|
A | G | 5 | a0001c0001t0003g0009a0001c0001t0003g0240a0001c0001t0003g0241others(2): Show | 6 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+6210T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134345 | ||||||
| chr1:119134570
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.90+5985C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134570 | ||||||
| chr1:119134627
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(108): Show | 113 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.90+5928G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134627 | ||||||
| chr1:119134896
|
T | C | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+5659A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134896 | ||||||
| chr1:119134930
|
T | C | 59 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(56): Show | 63 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.90+5625A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119134930 | ||||||
| chr1:119135279
|
T | A | 1 | a0001c0001t0001g0067 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.90+5276A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135279 | ||||||
| chr1:119135316
|
A | G | 1 | a0002c0002t0002g0114 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.90+5239T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135316 | ||||||
| chr1:119135420
|
A | C | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+5135T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135420 | ||||||
| chr1:119135698
|
T | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(201): Show | 212 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.90+4857A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135698 | ||||||
| chr1:119135711
|
T | C | 9 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(6): Show | 9 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+4844A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135711 | ||||||
| chr1:119135715
|
C | CAGAT | 16 | a0001c0001t0001g0313a0001c0001t0003g0231a0001c0001t0003g0232others(13): Show | 17 | HG01070.hp1 HG01074.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.90+4836_90+4839dup others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | ||||||
| chr1:119135715
|
C | CAGATAGA others(1): Show |
5 | a0001c0001t0006g0309a0001c0001t0006g0310a0001c0001t0006g0311others(2): Show | 5 | HG00738.hp2 HG03579.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+4832_90+4839dup others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | ||||||
| chr1:119135715
|
C | CAGATAGA others(5): Show |
1 | a0001c0001t0006g0308 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.90+4828_90+4839dup others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | ||||||
| chr1:119135715
|
C | T | 1 | a0001c0001t0015g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.90+4840G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | ||||||
| chr1:119135715
|
CAGAT | C | 40 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0003g0008others(37): Show | 41 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.90+4836_90+4839del others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | ||||||
| chr1:119135715
|
CAGATAGA others(1): Show |
C | 14 | a0001c0001t0003g0217a0001c0001t0003g0239a0001c0001t0003g0253others(11): Show | 14 | HG00438.hp2 HG00609.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.90+4832_90+4839del others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135715 | ||||||
| chr1:119135747
|
T | G | 8 | a0001c0001t0007g0020a0001c0003t0007g0227a0001c0003t0007g0228others(5): Show | 8 | HG02258.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.90+4808A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | ||||||
| chr1:119135747
|
T | TAGAG | 4 | a0001c0003t0007g0219a0001c0003t0007g0220a0001c0003t0007g0221others(1): Show | 4 | HG00741.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+4807_90+4808ins others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | ||||||
| chr1:119135747
|
T | TAGAGAGA others(5): Show |
1 | a0002c0002t0002g0209 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.90+4807_90+4808ins others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | ||||||
| chr1:119135747
|
T | TAGATAGA others(1): Show |
8 | a0001c0001t0007g0203a0001c0001t0007g0204a0001c0001t0007g0205others(5): Show | 8 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.90+4800_90+4807dup others(8): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | ||||||
| chr1:119135747
|
T | TAGATAGA others(5): Show |
2 | a0001c0001t0007g0201a0002c0002t0002g0200 | 2 | HG02027.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.90+4807_90+4808ins others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | ||||||
| chr1:119135747
|
T | TAGATAGA others(9): Show |
4 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(1): Show | 4 | NA18977.hp1 NA18989.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+4807_90+4808ins others(16): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | ||||||
| chr1:119135747
|
T | TAGATAGA others(13): Show |
1 | a0002c0002t0002g0196 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.90+4807_90+4808ins others(20): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | ||||||
| chr1:119135747
|
TAGATAGA others(7): Show |
T | 1 | a0001c0001t0004g0019 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.90+4794_90+4807del others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135747 | ||||||
| chr1:119135751
|
T | G | 1 | a0001c0001t0005g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.90+4804A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135751 | ||||||
| chr1:119135751
|
TAGAGAGA others(3): Show |
T | 2 | a0001c0001t0004g0017a0001c0001t0004g0018 | 2 | HG01433.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+4794_90+4803del others(10): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135751 | ||||||
| chr1:119135751
|
TAGAGAGA others(5): Show |
T | 2 | a0001c0001t0005g0263a0001c0001t0005g0264 | 2 | NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.90+4792_90+4803del others(12): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135751 | ||||||
| chr1:119135753
|
G | GAT | 79 | a0001c0001t0001g0028a0001c0001t0001g0068a0001c0001t0001g0070others(76): Show | 83 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.90+4801_90+4802ins others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135753 | ||||||
| chr1:119135755
|
G | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0029others(73): Show | 80 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.90+4800C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135755 | ||||||
| chr1:119135759
|
T | G | 79 | a0001c0001t0001g0028a0001c0001t0001g0068a0001c0001t0001g0070others(76): Show | 83 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.90+4796A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135759 | ||||||
| chr1:119135759
|
TAG | T | 33 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(30): Show | 33 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.90+4794_90+4795del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135759 | ||||||
| chr1:119135761
|
G | GAGAGAT | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0034others(62): Show | 69 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.90+4793_90+4794ins others(6): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135761 | ||||||
| chr1:119135761
|
G | GATAGAGA others(3): Show |
8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0033others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.90+4793_90+4794ins others(10): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135761 | ||||||
| chr1:119135761
|
G | GATAGATA others(7): Show |
2 | a0001c0001t0001g0029a0002c0002t0002g0120 | 2 | NA18964.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.90+4793_90+4794ins others(14): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135761 | ||||||
| chr1:119135761
|
G | GATAGATA others(11): Show |
1 | a0002c0002t0002g0119 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.90+4793_90+4794ins others(18): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135761 | ||||||
| chr1:119135761
|
G | T | 79 | a0001c0001t0001g0028a0001c0001t0001g0068a0001c0001t0001g0070others(76): Show | 83 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.90+4794C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135761 | ||||||
| chr1:119135763
|
G | T | 2 | a0001c0001t0005g0265a0001c0001t0005g0266 | 2 | HG00408.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.90+4792C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135763 | ||||||
| chr1:119135803
|
G | T | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(280): Show | 295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.90+4752C>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135803 | ||||||
| chr1:119135854
|
A | C | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(291): Show | 306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.90+4701T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135854 | ||||||
| chr1:119135866
|
G | A | 1 | a0001c0001t0008g0338 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.90+4689C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135866 | ||||||
| chr1:119135914
|
G | A | 1 | a0001c0001t0005g0117 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.90+4641C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135914 | ||||||
| chr1:119135914
|
GCATATGC | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(92): Show | 97 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.90+4634_90+4640del others(7): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135914 | ||||||
| chr1:119135915
|
C | T | 1 | a0001c0001t0005g0117 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.90+4640G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119135915 | ||||||
| chr1:119136061
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.90+4494G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136061 | ||||||
| chr1:119136126
|
C | CTG | 6 | a0001c0001t0003g0008a0001c0001t0003g0229a0001c0001t0003g0230others(3): Show | 7 | HG02080.hp1 NA19001.hp1 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.90+4427_90+4428dup others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136126 | ||||||
| chr1:119136245
|
CTT | C | 11 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(8): Show | 11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+4308_90+4309del others(2): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136245 | ||||||
| chr1:119136572
|
C | T | 1 | a0001c0001t0015g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.90+3983G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136572 | ||||||
| chr1:119136778
|
G | C | 338 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(335): Show | 352 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.90+3777C>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136778 | ||||||
| chr1:119136868
|
C | T | 1 | a0001c0001t0004g0171 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.90+3687G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136868 | ||||||
| chr1:119136981
|
ATAAC | A | 11 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(8): Show | 11 | HG00558.hp1 HG00609.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+3570_90+3573del others(4): Show |
WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119136981 | ||||||
| chr1:119137161
|
C | T | 18 | a0001c0001t0003g0008a0001c0001t0003g0229a0001c0001t0003g0230others(15): Show | 19 | HG00639.hp2 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.90+3394G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137161 | ||||||
| chr1:119137228
|
T | C | 7 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(4): Show | 7 | HG00408.hp1 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+3327A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137228 | ||||||
| chr1:119137344
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.90+3211A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137344 | ||||||
| chr1:119137443
|
C | T | 1 | a0001c0006t0004g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.90+3112G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137443 | ||||||
| chr1:119137467
|
T | C | 16 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0179others(13): Show | 18 | HG00423.hp2 HG02015.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.90+3088A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137467 | ||||||
| chr1:119137515
|
C | T | 135 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(132): Show | 141 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.90+3040G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137515 | ||||||
| chr1:119137600
|
T | C | 3 | a0001c0001t0004g0194a0002c0002t0002g0007a0002c0002t0002g0193 | 4 | NA18949.hp2 NA18964.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+2955A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137600 | ||||||
| chr1:119137673
|
C | T | 136 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(133): Show | 142 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.90+2882G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137673 | ||||||
| chr1:119137794
|
A | T | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG00558.hp1 NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.90+2761T>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119137794 | ||||||
| chr1:119138228
|
T | A | 8 | a0001c0001t0003g0267a0001c0001t0003g0268a0001c0001t0003g0269others(5): Show | 8 | HG00639.hp2 HG01361.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.90+2327A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138228 | ||||||
| chr1:119138344
|
A | G | 151 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(148): Show | 157 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.90+2211T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138344 | ||||||
| chr1:119138374
|
T | A | 152 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(149): Show | 158 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.90+2181A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138374 | ||||||
| chr1:119138411
|
C | A | 4 | a0001c0001t0016g0214a0003c0004t0005g0211a0003c0004t0005g0212others(1): Show | 4 | HG02630.hp2 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+2144G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138411 | ||||||
| chr1:119138892
|
T | C | 2 | a0001c0003t0007g0227a0001c0003t0007g0228 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.90+1663A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138892 | ||||||
| chr1:119138966
|
C | T | 72 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(69): Show | 76 | HG00438.hp1 HG00738.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.90+1589G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138966 | ||||||
| chr1:119138979
|
G | A | 10 | a0001c0001t0008g0276a0001c0001t0008g0277a0001c0001t0008g0278others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+1576C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119138979 | ||||||
| chr1:119139321
|
A | G | 3 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019 | 3 | HG01433.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.90+1234T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139321 | ||||||
| chr1:119139328
|
T | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | NA18944.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.90+1227A>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139328 | ||||||
| chr1:119139397
|
A | C | 1 | a0001c0001t0003g0217 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.90+1158T>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139397 | ||||||
| chr1:119139605
|
T | A | 135 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(132): Show | 141 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.90+950A>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139605 | ||||||
| chr1:119139747
|
T | C | 37 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(34): Show | 41 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.90+808A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139747 | ||||||
| chr1:119139801
|
A | G | 1 | a0001c0001t0006g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.90+754T>C | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119139801 | ||||||
| chr1:119140159
|
C | T | 1 | a0001c0003t0009g0021 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.90+396G>A | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140159 | ||||||
| chr1:119140297
|
C | A | 1 | a0002c0002t0002g0284 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.90+258G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140297 | ||||||
| chr1:119140336
|
C | A | 1 | a0001c0001t0004g0339 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.90+219G>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140336 | ||||||
| chr1:119140356
|
GA | G | 4 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(1): Show | 4 | HG01433.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+198delT | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140356 | ||||||
| chr1:119140440
|
G | A | 60 | a0001c0001t0001g0313a0001c0001t0001g0323a0001c0001t0001g0324others(57): Show | 64 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.90+115C>T | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140440 | ||||||
| chr1:119140547
|
T | C | 1 | a0001c0001t0008g0340 | 1 | HG03453.hp2 | splice_region_variant&intron_variant | LOW | c.90+8A>G | WARS2 | ENSG00000116874.12 | transcript | ENST00000235521.5 | protein_coding | 1/5 | chr1 | 119140547 |