Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g30990 | A10 | 22773596 | C | T | synonymous_variant | LOW | c.165C>T|p.Phe55Phe |
S19 |
2 | BAA10g30990 | A10 | 22773787 | C | T | missense_variant | MODERATE | c.356C>T|p.Pro119Leu |
S152 |
3 | BAA10g30990 | A10 | 22775889 | G | A | splice_region_variant&synonymous_variant | LOW | c.696G>A|p.Lys232Lys |
S219 S72 |