Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03700 | A02 | 1628998 | C | T | missense_variant&splice_region_variant | MODERATE | c.692G>A|p.Gly231Asp |
S104 |
2 | BAA02g03700 | A02 | 1629419 | G | A | synonymous_variant | LOW | c.513C>T|p.Ile171Ile |
S206 S26 |
3 | BAA02g03700 | A02 | 1633544 | C | T | upstream_gene_variant | MODIFIER | c.-3201G>A| |
S245 |