Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15960 | A01 | 7771792 | C | T | upstream_gene_variant | MODIFIER | c.-227C>T| |
S289 S290 |
2 | BAA01g15960 | A01 | 7774235 | C | T | missense_variant | MODERATE | c.991C>T|p.Leu331Phe |
S299 |
3 | BAA01g15960 | A01 | 7776501 | C | T | splice_region_variant&synonymous_variant | LOW | c.2113C>T|p.Leu705Leu |
S135 |
4 | BAA01g15960 | A01 | 7776605 | G | A | downstream_gene_variant | MODIFIER | c.*60G>A| |
S228 |