Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17050 | A10 | 16598180 | G | A | missense_variant | MODERATE | c.323G>A|p.Gly108Glu |
S125 |
2 | BAA10g17050 | A10 | 16599567 | G | A | missense_variant&splice_region_variant | MODERATE | c.1480G>A|p.Asp494Asn |
S291 |
3 | BAA10g17050 | A10 | 16599695 | C | T | synonymous_variant | LOW | c.1608C>T|p.Pro536Pro |
S34 |
4 | BAA10g17050 | A10 | 16600092 | G | A | missense_variant | MODERATE | c.1924G>A|p.Val642Met |
S303 |
5 | BAA10g17050 | A10 | 16600265 | C | T | synonymous_variant | LOW | c.2097C>T|p.Tyr699Tyr |
S142 |