Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01500 | A02 | 686603 | G | A | missense_variant | MODERATE | c.1559C>T|p.Ser520Phe |
S183 S198 |
2 | BAA02g01500 | A02 | 686882 | C | T | missense_variant | MODERATE | c.1280G>A|p.Gly427Asp |
S262 |
3 | BAA02g01500 | A02 | 687014 | G | A | missense_variant | MODERATE | c.1148C>T|p.Thr383Ile |
S291 |
4 | BAA02g01500 | A02 | 687617 | C | T | missense_variant | MODERATE | c.545G>A|p.Arg182Lys |
S284 |
5 | BAA02g01500 | A02 | 691133 | G | A | upstream_gene_variant | MODIFIER | c.-2972C>T| |
S98 |
6 | BAA02g01500 | A02 | 691252 | C | T | upstream_gene_variant | MODIFIER | c.-3091G>A| |
S181 |