Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07860 | A02 | 3383806 | G | A | missense_variant | MODERATE | c.2324C>T|p.Ser775Leu |
S239 |
2 | BAA02g07860 | A02 | 3383966 | G | A | synonymous_variant | LOW | c.2164C>T|p.Leu722Leu |
S176 |
3 | BAA02g07860 | A02 | 3386472 | C | T | missense_variant | MODERATE | c.616G>A|p.Glu206Lys |
S203 S273 S68 |
4 | BAA02g07860 | A02 | 3386558 | G | A | missense_variant | MODERATE | c.530C>T|p.Ser177Phe |
S169 |
5 | BAA02g07860 | A02 | 3387499 | C | T | upstream_gene_variant | MODIFIER | c.-236G>A| |
S257 |
6 | BAA02g07860 | A02 | 3388144 | G | A | upstream_gene_variant | MODIFIER | c.-881C>T| |
S82 S92 |
7 | BAA02g07860 | A02 | 3390680 | C | T | upstream_gene_variant | MODIFIER | c.-3417G>A| |
S16 |