| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g43860 | A09 | 49819450 | C | T | upstream_gene_variant | MODIFIER | c.-1911C>T| |
S83 S88 |
| 2 | BAA09g43860 | A09 | 49820344 | C | T | upstream_gene_variant | MODIFIER | c.-1017C>T| |
S51 |
| 3 | BAA09g43860 | A09 | 49820438 | C | T | upstream_gene_variant | MODIFIER | c.-923C>T| |
S296 |
| 4 | BAA09g43860 | A09 | 49821576 | G | A | splice_region_variant&intron_variant | LOW | c.211+5G>A| |
S280 |
| 5 | BAA09g43860 | A09 | 49823141 | C | T | synonymous_variant | LOW | c.978C>T|p.His326His |
S208 S93 |
| 6 | BAA09g43860 | A09 | 49824339 | C | T | stop_gained | HIGH | c.1918C>T|p.Gln640* |
S159 S243 S299 |
| 7 | BAA09g43860 | A09 | 49825158 | C | T | missense_variant | MODERATE | c.2651C>T|p.Ser884Leu |
S37 |
| 8 | BAA09g43860 | A09 | 49825167 | G | A | missense_variant&splice_region_variant | MODERATE | c.2660G>A|p.Ser887Asn |
S236 |
| 9 | BAA09g43860 | A09 | 49826213 | G | A | downstream_gene_variant | MODIFIER | c.*637G>A| |
S39 |