Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g06990 | A01 | 3088756 | C | T | synonymous_variant | LOW | c.786G>A|p.Gly262Gly |
S109 |
2 | BAA01g06990 | A01 | 3089310 | G | A | missense_variant | MODERATE | c.232C>T|p.Pro78Ser |
S295 |
3 | BAA01g06990 | A01 | 3093976 | C | T | upstream_gene_variant | MODIFIER | c.-4435G>A| |
S249 |