Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38730 | A02 | 32949290 | G | A | missense_variant | MODERATE | c.931C>T|p.Leu311Phe |
S166 |
2 | BAA02g38730 | A02 | 32950187 | C | T | missense_variant | MODERATE | c.466G>A|p.Glu156Lys |
S157 S163 |
3 | BAA02g38730 | A02 | 32950448 | C | A | missense_variant | MODERATE | c.205G>T|p.Ala69Ser |
|
4 | BAA02g38730 | A02 | 32950592 | T | C | missense_variant | MODERATE | c.61A>G|p.Asn21Asp |
S245 S246 |
5 | BAA02g38730 | A02 | 32954850 | C | T | upstream_gene_variant | MODIFIER | c.-4198G>A| |
S129 |