Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39290 | A02 | 33402422 | G | A | upstream_gene_variant | MODIFIER | c.-373G>A| |
S288 |
2 | BAA02g39290 | A02 | 33402458 | G | A | upstream_gene_variant | MODIFIER | c.-337G>A| |
S286 |
3 | BAA02g39290 | A02 | 33403130 | C | T | missense_variant | MODERATE | c.256C>T|p.Leu86Phe |
S63 |
4 | BAA02g39290 | A02 | 33404146 | G | A | missense_variant | MODERATE | c.785G>A|p.Arg262Lys |
S306 S308 |
5 | BAA02g39290 | A02 | 33404484 | C | T | synonymous_variant | LOW | c.1035C>T|p.Ile345Ile |
S289 S290 |
6 | BAA02g39290 | A02 | 33404552 | C | T | missense_variant | MODERATE | c.1103C>T|p.Ser368Phe |
S226 |
7 | BAA02g39290 | A02 | 33404823 | C | T | synonymous_variant | LOW | c.1296C>T|p.Ile432Ile |
S261 |
8 | BAA02g39290 | A02 | 33405375 | C | T | missense_variant | MODERATE | c.1568C>T|p.Ser523Phe |
S9 |
9 | BAA02g39290 | A02 | 33406359 | G | A | downstream_gene_variant | MODIFIER | c.*854G>A| |
S81 S85 |