Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g36400 | A08 | 22904113 | G | A | missense_variant | MODERATE | c.1594C>T|p.Pro532Ser |
S297 |
2 | BAA08g36400 | A08 | 22904366 | C | T | synonymous_variant | LOW | c.1428G>A|p.Gln476Gln |
S10 |
3 | BAA08g36400 | A08 | 22904814 | G | A | missense_variant | MODERATE | c.980C>T|p.Ser327Phe |
S106 |