Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39250 | A01 | 26064183 | C | T | missense_variant | MODERATE | c.889C>T|p.Pro297Ser |
S186 |
2 | BAA01g39250 | A01 | 26064323 | C | T | synonymous_variant | LOW | c.945C>T|p.Tyr315Tyr |
S249 |
3 | BAA01g39250 | A01 | 26065374 | G | A | missense_variant | MODERATE | c.1996G>A|p.Ala666Thr |
S138 |
4 | BAA01g39250 | A01 | 26065474 | C | T | missense_variant | MODERATE | c.2096C>T|p.Ala699Val |
S206 S26 |