Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27500 | A02 | 15470470 | G | A | missense_variant | MODERATE | c.316G>A|p.Asp106Asn |
S281 |
2 | BAA02g27500 | A02 | 15471026 | G | A | missense_variant | MODERATE | c.872G>A|p.Gly291Glu |
S173 |
3 | BAA02g27500 | A02 | 15471101 | G | A | missense_variant | MODERATE | c.947G>A|p.Arg316His |
S100 |
4 | BAA02g27500 | A02 | 15471181 | C | T | missense_variant | MODERATE | c.1027C>T|p.Pro343Ser |
S32 |
5 | BAA02g27500 | A02 | 15471974 | C | T | synonymous_variant | LOW | c.1497C>T|p.Leu499Leu |
S156 S3 S34 |
6 | BAA02g27500 | A02 | 15471992 | G | A | synonymous_variant | LOW | c.1515G>A|p.Ala505Ala |
S249 |
7 | BAA02g27500 | A02 | 15472450 | G | A | missense_variant | MODERATE | c.1747G>A|p.Asp583Asn |
S209 |
8 | BAA02g27500 | A02 | 15473167 | G | A | synonymous_variant | LOW | c.2280G>A|p.Gln760Gln |
S68 |