Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01050 | A08 | 765169 | C | T | missense_variant | MODERATE | c.182C>T|p.Pro61Leu |
S243 S299 |
2 | BAA08g01050 | A08 | 765368 | C | T | missense_variant | MODERATE | c.292C>T|p.Pro98Ser |
S272 |
3 | BAA08g01050 | A08 | 765557 | C | T | synonymous_variant | LOW | c.390C>T|p.Arg130Arg |
S205 |