Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04960 | A02 | 2168574 | G | A | synonymous_variant | LOW | c.459G>A|p.Glu153Glu |
S36 |
2 | BAA02g04960 | A02 | 2169489 | C | T | splice_region_variant&intron_variant | LOW | c.966-6C>T| |
S79 S84 |
3 | BAA02g04960 | A02 | 2170536 | C | T | missense_variant | MODERATE | c.1486C>T|p.Leu496Phe |
S32 |