Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g67170 | A09 | 60997630 | C | T | missense_variant | MODERATE | c.527C>T|p.Ala176Val |
S131 |
2 | BAA09g67170 | A09 | 60997705 | G | A | missense_variant | MODERATE | c.602G>A|p.Ser201Asn |
S4 |
3 | BAA09g67170 | A09 | 60998373 | C | T | stop_gained | HIGH | c.886C>T|p.Gln296* |
S159 S299 |