Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g33880 | A09 | 42364932 | C | T | missense_variant | MODERATE | c.139C>T|p.Leu47Phe |
S269 |
2 | BAA09g33880 | A09 | 42367968 | C | T | downstream_gene_variant | MODIFIER | c.*2616C>T| |
S303 |
3 | BAA09g33880 | A09 | 42368518 | C | T | downstream_gene_variant | MODIFIER | c.*3166C>T| |
S212 |