Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09290 | A02 | 4099706 | C | T | upstream_gene_variant | MODIFIER | c.-2222C>T| |
S278 |
2 | BAA02g09290 | A02 | 4101418 | C | T | upstream_gene_variant | MODIFIER | c.-510C>T| |
S241 |
3 | BAA02g09290 | A02 | 4101979 | C | T | missense_variant | MODERATE | c.52C>T|p.Pro18Ser |
S118 |
4 | BAA02g09290 | A02 | 4103032 | G | A | missense_variant | MODERATE | c.878G>A|p.Gly293Glu |
S173 |