Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00080 | A09 | 218787 | C | T | synonymous_variant | LOW | c.312C>T|p.Pro104Pro |
S70 |
2 | BAA09g00080 | A09 | 218806 | G | A | missense_variant | MODERATE | c.331G>A|p.Asp111Asn |
S200 |
3 | BAA09g00080 | A09 | 218852 | G | A | missense_variant | MODERATE | c.377G>A|p.Gly126Glu |
S65 |
4 | BAA09g00080 | A09 | 221727 | C | T | intron_variant | MODIFIER | c.553-345C>T| |
S255 |