Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01230 | A02 | 573186 | C | T | missense_variant | MODERATE | c.902G>A|p.Gly301Glu |
S202 |
2 | BAA02g01230 | A02 | 573439 | C | T | synonymous_variant | LOW | c.738G>A|p.Leu246Leu |
S241 |
3 | BAA02g01230 | A02 | 573608 | G | A | synonymous_variant | LOW | c.636C>T|p.Ser212Ser |
S236 |
4 | BAA02g01230 | A02 | 574232 | C | T | missense_variant | MODERATE | c.169G>A|p.Glu57Lys |
S177 |
5 | BAA02g01230 | A02 | 579035 | G | A | upstream_gene_variant | MODIFIER | c.-4635C>T| |
S158 |