Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g20790 | A08 | 15927700 | C | T | missense_variant | MODERATE | c.47C>T|p.Ala16Val |
S168 |
2 | BAA08g20790 | A08 | 15929415 | C | T | synonymous_variant | LOW | c.1557C>T|p.Arg519Arg |
S144 |
3 | BAA08g20790 | A08 | 15929606 | G | A | missense_variant | MODERATE | c.1748G>A|p.Gly583Asp |
S128 |
4 | BAA08g20790 | A08 | 15929724 | G | A | stop_gained | HIGH | c.1866G>A|p.Trp622* |
S266 |
5 | BAA08g20790 | A08 | 15930835 | G | A | stop_gained | HIGH | c.2883G>A|p.Trp961* |
S48 |