Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46960 | A09 | 51477551 | C | T | missense_variant | MODERATE | c.145C>T|p.Leu49Phe |
S62 |
2 | BAA09g46960 | A09 | 51479412 | G | A | downstream_gene_variant | MODIFIER | c.*1844G>A| |
S231 |
3 | BAA09g46960 | A09 | 51479862 | G | A | downstream_gene_variant | MODIFIER | c.*2294G>A| |
S135 |
4 | BAA09g46960 | A09 | 51481334 | A | G | downstream_gene_variant | MODIFIER | c.*3766A>G| |
S288 |