| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g09260 | A02 | 4091091 | G | A | missense_variant | MODERATE | c.1216C>T|p.Leu406Phe |
S37 |
| 2 | BAA02g09260 | A02 | 4091589 | G | A | splice_region_variant&intron_variant | LOW | c.975+8C>T| |
S53 S81 |
| 3 | BAA02g09260 | A02 | 4092015 | C | T | splice_region_variant&intron_variant | LOW | c.652-4G>A| |
S284 |
| 4 | BAA02g09260 | A02 | 4093419 | G | A | synonymous_variant | LOW | c.174C>T|p.Ala58Ala |
S79 S91 |
| 5 | BAA02g09260 | A02 | 4093502 | C | T | missense_variant | MODERATE | c.91G>A|p.Gly31Arg |
S262 |
| 6 | BAA02g09260 | A02 | 4095243 | C | T | upstream_gene_variant | MODIFIER | c.-1651G>A| |
S273 |
| 7 | BAA02g09260 | A02 | 4095808 | C | T | upstream_gene_variant | MODIFIER | c.-2216G>A| |
S255 |
| 8 | BAA02g09260 | A02 | 4098583 | C | T | upstream_gene_variant | MODIFIER | c.-4991G>A| |
S226 |