Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01540 | A10 | 765471 | C | T | missense_variant | MODERATE | c.611C>T|p.Ser204Phe |
S125 |
2 | BAA10g01540 | A10 | 765503 | C | T | synonymous_variant | LOW | c.643C>T|p.Leu215Leu |
S206 S26 |
3 | BAA10g01540 | A10 | 766501 | G | A | synonymous_variant | LOW | c.1347G>A|p.Gln449Gln |
S76 |