Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46120 | A09 | 51036032 | A | T | missense_variant | MODERATE | c.336A>T|p.Arg112Ser |
|
2 | BAA09g46120 | A09 | 51036595 | C | T | missense_variant | MODERATE | c.475C>T|p.Pro159Ser |
S301 S304 |
3 | BAA09g46120 | A09 | 51038643 | C | T | downstream_gene_variant | MODIFIER | c.*2031C>T| |
S279 |
4 | BAA09g46120 | A09 | 51039477 | C | T | downstream_gene_variant | MODIFIER | c.*2865C>T| |
S133 |
5 | BAA09g46120 | A09 | 51041178 | C | T | downstream_gene_variant | MODIFIER | c.*4566C>T| |
S173 |