Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22400 | A09 | 14009821 | C | T | missense_variant | MODERATE | c.478C>T|p.Pro160Ser |
S11 |
2 | BAA09g22400 | A09 | 14013575 | C | T | downstream_gene_variant | MODIFIER | c.*3623C>T| |
S168 |
3 | BAA09g22400 | A09 | 14013739 | C | T | downstream_gene_variant | MODIFIER | c.*3787C>T| |
S6 |
4 | BAA09g22400 | A09 | 14014908 | C | T | downstream_gene_variant | MODIFIER | c.*4956C>T| |
S228 |