Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g40960 | A05 | 39388475 | C | T | missense_variant | MODERATE | c.131C>T|p.Thr44Ile |
S203 |
2 | BAA05g40960 | A05 | 39388512 | C | T | synonymous_variant | LOW | c.168C>T|p.Val56Val |
S219 |
3 | BAA05g40960 | A05 | 39388756 | G | A | missense_variant | MODERATE | c.412G>A|p.Gly138Ser |
S191 |
4 | BAA05g40960 | A05 | 39389462 | C | T | synonymous_variant | LOW | c.1011C>T|p.Tyr337Tyr |
S178 |
5 | BAA05g40960 | A05 | 39392610 | C | A | downstream_gene_variant | MODIFIER | c.*2692C>A| |
S224 |