Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g19900 | A03 | 8837393 | C | T | missense_variant | MODERATE | c.1130C>T|p.Ala377Val |
S131 |
2 | BAA03g19900 | A03 | 8840825 | G | A | downstream_gene_variant | MODIFIER | c.*3326G>A| |
S186 |
3 | BAA03g19900 | A03 | 8840847 | C | T | downstream_gene_variant | MODIFIER | c.*3348C>T| |
S216 |