Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20270 | A01 | 9953167 | C | T | missense_variant | MODERATE | c.499C>T|p.Leu167Phe |
S41 |
2 | BAA01g20270 | A01 | 9953343 | C | T | synonymous_variant | LOW | c.675C>T|p.Leu225Leu |
S153 S273 |
3 | BAA01g20270 | A01 | 9953421 | G | A | synonymous_variant | LOW | c.753G>A|p.Ser251Ser |
S162 |