Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44390 | A09 | 50088000 | G | A | missense_variant | MODERATE | c.700C>T|p.Leu234Phe |
S48 |
2 | BAA09g44390 | A09 | 50088180 | G | A | missense_variant | MODERATE | c.542C>T|p.Ala181Val |
S62 |
3 | BAA09g44390 | A09 | 50088341 | C | T | synonymous_variant | LOW | c.381G>A|p.Glu127Glu |
S289 |
4 | BAA09g44390 | A09 | 50090802 | C | T | upstream_gene_variant | MODIFIER | c.-2081G>A| |
S28 |
5 | BAA09g44390 | A09 | 50091225 | G | A | upstream_gene_variant | MODIFIER | c.-2504C>T| |
S190 |
6 | BAA09g44390 | A09 | 50092548 | G | A | upstream_gene_variant | MODIFIER | c.-3827C>T| |
S270 |