Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44030 | A09 | 49902639 | C | T | missense_variant | MODERATE | c.1472G>A|p.Gly491Glu |
S77 S82 |
2 | BAA09g44030 | A09 | 49902971 | G | A | synonymous_variant | LOW | c.1140C>T|p.Phe380Phe |
S42 |
3 | BAA09g44030 | A09 | 49908210 | G | A | upstream_gene_variant | MODIFIER | c.-4100C>T| |
S171 |