Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05690 | A02 | 2441843 | C | T | missense_variant | MODERATE | c.418C>T|p.Leu140Phe |
S287 |
2 | BAA02g05690 | A02 | 2442292 | G | A | missense_variant&splice_region_variant | MODERATE | c.712G>A|p.Asp238Asn |
S84 S93 |
3 | BAA02g05690 | A02 | 2442492 | C | T | splice_region_variant&intron_variant | LOW | c.831+6C>T| |
S117 |
4 | BAA02g05690 | A02 | 2442876 | G | A | missense_variant | MODERATE | c.1055G>A|p.Gly352Glu |
S98 |