Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g43120 | A01 | 28515689 | C | T | missense_variant | MODERATE | c.809G>A|p.Gly270Glu |
S18 |
2 | BAA01g43120 | A01 | 28517885 | G | A | synonymous_variant | LOW | c.327C>T|p.Cys109Cys |
S2 |
3 | BAA01g43120 | A01 | 28517980 | C | T | missense_variant | MODERATE | c.232G>A|p.Ala78Thr |
S48 |
4 | BAA01g43120 | A01 | 28518646 | C | T | upstream_gene_variant | MODIFIER | c.-185G>A| |
S183 S198 |
5 | BAA01g43120 | A01 | 28518753 | C | T | upstream_gene_variant | MODIFIER | c.-292G>A| |
S132 S215 S89 |
6 | BAA01g43120 | A01 | 28518904 | G | A | upstream_gene_variant | MODIFIER | c.-443C>T| |
S294 |
7 | BAA01g43120 | A01 | 28519346 | G | A | upstream_gene_variant | MODIFIER | c.-885C>T| |
S43 |
8 | BAA01g43120 | A01 | 28520506 | T | C | upstream_gene_variant | MODIFIER | c.-2045A>G| |
S6 |
9 | BAA01g43120 | A01 | 28521691 | C | T | upstream_gene_variant | MODIFIER | c.-3230G>A| |
S94 |