Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14590 | A02 | 6809749 | C | T | missense_variant | MODERATE | c.1159G>A|p.Glu387Lys |
S278 |
2 | BAA02g14590 | A02 | 6810302 | G | A | synonymous_variant | LOW | c.681C>T|p.Phe227Phe |
S105 S106 |
3 | BAA02g14590 | A02 | 6810972 | G | A | missense_variant | MODERATE | c.245C>T|p.Ala82Val |
S123 |
4 | BAA02g14590 | A02 | 6813917 | C | T | upstream_gene_variant | MODIFIER | c.-2533G>A| |
S205 S240 |
5 | BAA02g14590 | A02 | 6814043 | C | T | upstream_gene_variant | MODIFIER | c.-2659G>A| |
S262 |
6 | BAA02g14590 | A02 | 6814174 | G | A | upstream_gene_variant | MODIFIER | c.-2790C>T| |
S158 |
7 | BAA02g14590 | A02 | 6815431 | G | A | upstream_gene_variant | MODIFIER | c.-4047C>T| |
S287 |