Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00700 | A09 | 600924 | C | T | missense_variant | MODERATE | c.571G>A|p.Asp191Asn |
S182 |
2 | BAA09g00700 | A09 | 601406 | C | T | splice_donor_variant&intron_variant | HIGH | c.378+1G>A| |
S68 |
3 | BAA09g00700 | A09 | 601565 | G | A | stop_gained | HIGH | c.220C>T|p.Gln74* |
S245 |
4 | BAA09g00700 | A09 | 601647 | C | T | synonymous_variant | LOW | c.138G>A|p.Glu46Glu |
S59 |