Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18450 | A09 | 11097573 | T | A | splice_region_variant&intron_variant | LOW | c.521+8T>A| |
S74 |
2 | BAA09g18450 | A09 | 11098992 | G | T | missense_variant | MODERATE | c.1073G>T|p.Arg358Leu |
S289 S290 |
3 | BAA09g18450 | A09 | 11099400 | C | T | missense_variant | MODERATE | c.1481C>T|p.Ala494Val |
S37 |