Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19940 | A02 | 10468877 | A | C | missense_variant | MODERATE | c.296A>C|p.Asn99Thr |
S126 S228 S239 S243 S257 S260 S286 S99 |
2 | BAA02g19940 | A02 | 10469044 | C | T | stop_gained | HIGH | c.463C>T|p.Gln155* |
S114 S242 |
3 | BAA02g19940 | A02 | 10469476 | C | T | synonymous_variant | LOW | c.783C>T|p.Asp261Asp |
S81 |
4 | BAA02g19940 | A02 | 10469477 | G | A | missense_variant | MODERATE | c.784G>A|p.Glu262Lys |
S113 |
5 | BAA02g19940 | A02 | 10469710 | C | T | stop_gained | HIGH | c.916C>T|p.Gln306* |
S38 |
6 | BAA02g19940 | A02 | 10469856 | G | A | synonymous_variant | LOW | c.1062G>A|p.Ala354Ala |
S51 |