Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g20760 | A08 | 15916161 | C | T | missense_variant | MODERATE | c.1582G>A|p.Asp528Asn |
S120 |
2 | BAA08g20760 | A08 | 15916282 | C | T | synonymous_variant | LOW | c.1461G>A|p.Thr487Thr |
S277 |
3 | BAA08g20760 | A08 | 15916347 | C | T | missense_variant | MODERATE | c.1396G>A|p.Glu466Lys |
S178 |
4 | BAA08g20760 | A08 | 15918079 | G | A | missense_variant | MODERATE | c.487C>T|p.Pro163Ser |
S62 |