Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09190 | A05 | 4588457 | C | T | synonymous_variant | LOW | c.282C>T|p.Val94Val |
S143 |
2 | BAA05g09190 | A05 | 4589915 | G | A | missense_variant&splice_region_variant | MODERATE | c.1057G>A|p.Val353Ile |
S41 |
3 | BAA05g09190 | A05 | 4590087 | C | T | intron_variant | MODIFIER | c.1197+32C>T| |
S76 |