Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00090 | A07 | 41363 | C | T | missense_variant | MODERATE | c.557G>A|p.Gly186Glu |
S287 |
2 | BAA07g00090 | A07 | 41522 | C | T | missense_variant | MODERATE | c.478G>A|p.Ala160Thr |
S1 |
3 | BAA07g00090 | A07 | 42819 | C | T | upstream_gene_variant | MODIFIER | c.-82G>A| |
S301 |