| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 12051 | BAA01g09640 | A01 | 4298425 | C | T | upstream_gene_variant | MODIFIER | c.-3292C>T| |
S26 |
| 12052 | BAA01g09640 | A01 | 4298632 | G | A | upstream_gene_variant | MODIFIER | c.-3085G>A| |
S159 S243 |
| 12053 | BAA01g09640 | A01 | 4300441 | G | A | upstream_gene_variant | MODIFIER | c.-1276G>A| |
S181 |
| 12054 | BAA01g09640 | A01 | 4300980 | G | A | upstream_gene_variant | MODIFIER | c.-737G>A| |
S247 |
| 12055 | BAA01g09640 | A01 | 4301154 | G | A | upstream_gene_variant | MODIFIER | c.-563G>A| |
S257 |
| 12056 | BAA01g09640 | A01 | 4301594 | C | T | upstream_gene_variant | MODIFIER | c.-123C>T| |
S97 |
| 12057 | BAA01g09640 | A01 | 4302058 | G | C | downstream_gene_variant | MODIFIER | c.*123G>C| |
S125 |
| 12058 | BAA01g09640 | A01 | 4302159 | C | T | downstream_gene_variant | MODIFIER | c.*224C>T| |
S263 |
| 12059 | BAA01g09640 | A01 | 4302723 | G | A | downstream_gene_variant | MODIFIER | c.*788G>A| |
S3 |
| 12060 | BAA01g09650 | A01 | 4307263 | C | T | synonymous_variant | LOW | c.630G>A|p.Pro210Pro |
S118 |
| 12061 | BAA01g09650 | A01 | 4307602 | C | T | stop_gained | HIGH | c.291G>A|p.Trp97* |
S205 |
| 12062 | BAA01g09650 | A01 | 4309717 | G | A | upstream_gene_variant | MODIFIER | c.-1750C>T| |
S97 |
| 12063 | BAA01g09660 | A01 | 4310857 | C | T | splice_region_variant&synonymous_variant | LOW | c.3312G>A|p.Glu1104Glu |
S135 |
| 12064 | BAA01g09650 | A01 | 4311046 | C | T | upstream_gene_variant | MODIFIER | c.-3079G>A| |
S198 |
| 12065 | BAA01g09660 | A01 | 4312495 | G | A | synonymous_variant | LOW | c.2533C>T|p.Leu845Leu |
S146 |
| 12066 | BAA01g09660 | A01 | 4313200 | G | A | splice_region_variant&intron_variant | LOW | c.2130+4C>T| |
S287 |
| 12067 | BAA01g09660 | A01 | 4313265 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2070-1G>A| |
S286 |
| 12068 | BAA01g09660 | A01 | 4313558 | C | T | missense_variant | MODERATE | c.1936G>A|p.Val646Ile |
S153 S213 |
| 12069 | BAA01g09660 | A01 | 4314164 | G | A | intron_variant | MODIFIER | c.1530-17C>T| |
S201 |
| 12070 | BAA01g09660 | A01 | 4314601 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1332-1G>A| |
S100 |
| 12071 | BAA01g09670 | A01 | 4315130 | G | A | downstream_gene_variant | MODIFIER | c.*4040C>T| |
S10 |
| 12072 | BAA01g09660 | A01 | 4315458 | C | T | missense_variant | MODERATE | c.1036G>A|p.Asp346Asn |
S71 |
| 12073 | BAA01g09670 | A01 | 4316102 | G | A | downstream_gene_variant | MODIFIER | c.*3068C>T| |
S279 |
| 12074 | BAA01g09670 | A01 | 4317241 | C | T | downstream_gene_variant | MODIFIER | c.*1929G>A| |
S16 |
| 12075 | BAA01g09660 | A01 | 4318185 | G | A | upstream_gene_variant | MODIFIER | c.-419C>T| |
S289 S290 |