Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46090 | A02 | 37561202 | G | A | upstream_gene_variant | MODIFIER | c.-4567G>A| |
S283 |
2 | BAA02g46090 | A02 | 37563892 | G | A | upstream_gene_variant | MODIFIER | c.-1877G>A| |
S297 |
3 | BAA02g46090 | A02 | 37564049 | C | T | upstream_gene_variant | MODIFIER | c.-1720C>T| |
S192 |
4 | BAA02g46090 | A02 | 37564249 | C | T | upstream_gene_variant | MODIFIER | c.-1520C>T| |
S206 S26 |
5 | BAA02g46090 | A02 | 37565057 | C | T | upstream_gene_variant | MODIFIER | c.-712C>T| |
S23 |
6 | BAA02g46090 | A02 | 37565642 | G | A | upstream_gene_variant | MODIFIER | c.-127G>A| |
S70 |
7 | BAA02g46090 | A02 | 37565803 | C | T | missense_variant | MODERATE | c.35C>T|p.Pro12Leu |
S262 |
8 | BAA02g46090 | A02 | 37566047 | G | A | synonymous_variant | LOW | c.279G>A|p.Glu93Glu |
S53 |
9 | BAA02g46090 | A02 | 37566350 | G | A | synonymous_variant | LOW | c.582G>A|p.Glu194Glu |
S66 |