Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01050 | A02 | 480970 | C | T | synonymous_variant | LOW | c.37C>T|p.Leu13Leu |
S278 |
2 | BAA02g01050 | A02 | 481274 | C | T | synonymous_variant | LOW | c.234C>T|p.Gly78Gly |
S216 |
3 | BAA02g01050 | A02 | 483085 | G | A | missense_variant | MODERATE | c.883G>A|p.Gly295Ser |
S69 |
4 | BAA02g01050 | A02 | 483244 | C | T | missense_variant | MODERATE | c.1042C>T|p.Leu348Phe |
S240 |