Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11490 | A09 | 6453551 | C | T | synonymous_variant | LOW | c.261C>T|p.Ser87Ser |
S9 |
2 | BAA09g11490 | A09 | 6453965 | C | T | missense_variant | MODERATE | c.541C>T|p.Leu181Phe |
S111 |
3 | BAA09g11490 | A09 | 6456158 | C | T | synonymous_variant | LOW | c.1635C>T|p.Phe545Phe |
S18 |