Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18740 | A10 | 17443433 | C | T | upstream_gene_variant | MODIFIER | c.-635C>T| |
S210 |
2 | BAA10g18740 | A10 | 17443795 | G | A | upstream_gene_variant | MODIFIER | c.-273G>A| |
S111 |
3 | BAA10g18740 | A10 | 17446138 | G | A | missense_variant | MODERATE | c.778G>A|p.Ala260Thr |
S270 |