Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11150 | A01 | 5146583 | C | T | missense_variant | MODERATE | c.122C>T|p.Ser41Leu |
S2 |
2 | BAA01g11150 | A01 | 5147403 | G | A | missense_variant | MODERATE | c.607G>A|p.Ala203Thr |
S17 |
3 | BAA01g11150 | A01 | 5147681 | G | A | synonymous_variant | LOW | c.885G>A|p.Gln295Gln |
S252 |
4 | BAA01g11150 | A01 | 5148742 | G | A | synonymous_variant | LOW | c.1542G>A|p.Glu514Glu |
S12 |
5 | BAA01g11150 | A01 | 5152535 | G | A | downstream_gene_variant | MODIFIER | c.*3197G>A| |
S116 |
6 | BAA01g11150 | A01 | 5152594 | T | C | downstream_gene_variant | MODIFIER | c.*3256T>C| |
S153 S257 |