Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17880 | A02 | 8950598 | G | A | missense_variant | MODERATE | c.97G>A|p.Glu33Lys |
S50 |
2 | BAA02g17880 | A02 | 8950655 | G | A | missense_variant | MODERATE | c.154G>A|p.Asp52Asn |
S107 |
3 | BAA02g17880 | A02 | 8951077 | G | A | synonymous_variant | LOW | c.576G>A|p.Leu192Leu |
S263 |
4 | BAA02g17880 | A02 | 8951078 | C | T | synonymous_variant | LOW | c.577C>T|p.Leu193Leu |
S283 |
5 | BAA02g17880 | A02 | 8951500 | C | T | synonymous_variant | LOW | c.999C>T|p.Ile333Ile |
S270 |
6 | BAA02g17880 | A02 | 8951750 | C | T | downstream_gene_variant | MODIFIER | c.*100C>T| |
S40 S49 |
7 | BAA02g17880 | A02 | 8952970 | C | T | downstream_gene_variant | MODIFIER | c.*1320C>T| |
S180 |
8 | BAA02g17880 | A02 | 8953343 | G | A | downstream_gene_variant | MODIFIER | c.*1693G>A| |
S260 |
9 | BAA02g17880 | A02 | 8953550 | C | T | downstream_gene_variant | MODIFIER | c.*1900C>T| |
S225 |