Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17080 | A09 | 10139172 | C | T | missense_variant | MODERATE | c.1240G>A|p.Ala414Thr |
S173 |
2 | BAA09g17080 | A09 | 10139540 | C | T | missense_variant | MODERATE | c.872G>A|p.Gly291Glu |
S64 |
3 | BAA09g17080 | A09 | 10140402 | G | A | synonymous_variant | LOW | c.10C>T|p.Leu4Leu |
S308 |
4 | BAA09g17080 | A09 | 10143711 | C | T | upstream_gene_variant | MODIFIER | c.-3300G>A| |
S132 S137 S215 S89 |