Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10090 | A02 | 4451177 | G | A | missense_variant&splice_region_variant | MODERATE | c.550G>A|p.Glu184Lys |
S173 |
2 | BAA02g10090 | A02 | 4451516 | C | T | missense_variant | MODERATE | c.725C>T|p.Ala242Val |
S144 |
3 | BAA02g10090 | A02 | 4451542 | G | A | missense_variant | MODERATE | c.751G>A|p.Asp251Asn |
S146 |
4 | BAA02g10090 | A02 | 4453885 | G | A | downstream_gene_variant | MODIFIER | c.*788G>A| |
S45 |
5 | BAA02g10090 | A02 | 4454567 | C | T | downstream_gene_variant | MODIFIER | c.*1470C>T| |
S77 S82 |
6 | BAA02g10090 | A02 | 4455340 | C | T | downstream_gene_variant | MODIFIER | c.*2243C>T| |
S272 |
7 | BAA02g10090 | A02 | 4456312 | G | A | downstream_gene_variant | MODIFIER | c.*3215G>A| |
S51 |