Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02160 | A02 | 970498 | C | T | synonymous_variant | LOW | c.147C>T|p.Asn49Asn |
S255 |
2 | BAA02g02160 | A02 | 970662 | G | A | missense_variant | MODERATE | c.311G>A|p.Cys104Tyr |
S157 |
3 | BAA02g02160 | A02 | 971015 | C | T | stop_gained | HIGH | c.664C>T|p.Arg222* |
S100 |
4 | BAA02g02160 | A02 | 971065 | C | T | synonymous_variant | LOW | c.714C>T|p.Thr238Thr |
S71 |
5 | BAA02g02160 | A02 | 973493 | G | A | downstream_gene_variant | MODIFIER | c.*2383G>A| |
S209 |
6 | BAA02g02160 | A02 | 973579 | G | A | downstream_gene_variant | MODIFIER | c.*2469G>A| |
S146 |