Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01870 | A02 | 821383 | C | T | upstream_gene_variant | MODIFIER | c.-822C>T| |
S144 |
2 | BAA02g01870 | A02 | 821418 | G | A | upstream_gene_variant | MODIFIER | c.-787G>A| |
S98 |
3 | BAA02g01870 | A02 | 823618 | G | A | missense_variant | MODERATE | c.649G>A|p.Ala217Thr |
S192 |
4 | BAA02g01870 | A02 | 823635 | G | A | synonymous_variant | LOW | c.666G>A|p.Arg222Arg |
S202 |
5 | BAA02g01870 | A02 | 825214 | G | A | synonymous_variant | LOW | c.1554G>A|p.Glu518Glu |
S303 |