Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09040 | A02 | 3999297 | C | T | missense_variant | MODERATE | c.517C>T|p.Pro173Ser |
S18 |
2 | BAA02g09040 | A02 | 3999546 | C | T | stop_gained | HIGH | c.697C>T|p.Gln233* |
S263 |
3 | BAA02g09040 | A02 | 3999691 | C | T | missense_variant | MODERATE | c.842C>T|p.Ala281Val |
S293 |
4 | BAA02g09040 | A02 | 3999738 | G | A | missense_variant | MODERATE | c.889G>A|p.Glu297Lys |
S202 |
5 | BAA02g09040 | A02 | 4000050 | C | T | synonymous_variant | LOW | c.1113C>T|p.Val371Val |
S120 |