Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35800 | A09 | 44111010 | C | T | missense_variant | MODERATE | c.2206G>A|p.Glu736Lys |
S168 |
2 | BAA09g35800 | A09 | 44111191 | C | T | synonymous_variant | LOW | c.2025G>A|p.Ala675Ala |
S9 |
3 | BAA09g35800 | A09 | 44112612 | G | A | synonymous_variant | LOW | c.1542C>T|p.Tyr514Tyr |
S231 |
4 | BAA09g35800 | A09 | 44118413 | G | A | upstream_gene_variant | MODIFIER | c.-1209C>T| |
S274 |
5 | BAA09g35800 | A09 | 44119810 | G | A | upstream_gene_variant | MODIFIER | c.-2606C>T| |
S89 |