Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10790 | A02 | 4826213 | G | A | missense_variant | MODERATE | c.317G>A|p.Arg106Lys |
S53 |
2 | BAA02g10790 | A02 | 4827474 | C | T | missense_variant | MODERATE | c.1334C>T|p.Pro445Leu |
S299 |
3 | BAA02g10790 | A02 | 4827605 | C | T | missense_variant | MODERATE | c.1465C>T|p.Pro489Ser |
S171 |
4 | BAA02g10790 | A02 | 4828153 | C | T | synonymous_variant | LOW | c.2013C>T|p.Ile671Ile |
S157 |
5 | BAA02g10790 | A02 | 4828307 | C | T | missense_variant | MODERATE | c.2167C>T|p.Leu723Phe |
S32 |
6 | BAA02g10790 | A02 | 4828363 | C | T | synonymous_variant | LOW | c.2223C>T|p.Ile741Ile |
S255 |