Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02270 | A10 | 1077976 | C | T | missense_variant | MODERATE | c.602G>A|p.Gly201Asp |
S244 |
2 | BAA10g02270 | A10 | 1078099 | C | T | missense_variant | MODERATE | c.559G>A|p.Gly187Arg |
S135 |
3 | BAA10g02270 | A10 | 1083940 | C | T | upstream_gene_variant | MODIFIER | c.-4746G>A| |
S20 |