Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29860 | A02 | 17154329 | G | A | missense_variant | MODERATE | c.1292C>T|p.Thr431Ile |
S134 |
2 | BAA02g29860 | A02 | 17157130 | C | T | synonymous_variant | LOW | c.165G>A|p.Gln55Gln |
S138 |
3 | BAA02g29860 | A02 | 17158041 | G | A | upstream_gene_variant | MODIFIER | c.-623C>T| |
S281 |