Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14490 | A08 | 12364930 | G | A | missense_variant | MODERATE | c.1973C>T|p.Ala658Val |
S286 |
2 | BAA08g14490 | A08 | 12366914 | G | A | synonymous_variant | LOW | c.996C>T|p.Phe332Phe |
S109 |
3 | BAA08g14490 | A08 | 12372001 | C | T | upstream_gene_variant | MODIFIER | c.-2108G>A| |
S1 S90 |