Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41100 | A05 | 39421354 | G | A | missense_variant | MODERATE | c.656C>T|p.Ala219Val |
S125 |
2 | BAA05g41100 | A05 | 39421633 | G | A | missense_variant | MODERATE | c.466C>T|p.Leu156Phe |
S2 |
3 | BAA05g41100 | A05 | 39425437 | C | T | upstream_gene_variant | MODIFIER | c.-2676G>A| |
S239 |
4 | BAA05g41100 | A05 | 39427333 | G | A | upstream_gene_variant | MODIFIER | c.-4572C>T| |
S149 |
5 | BAA05g41100 | A05 | 39427456 | G | A | upstream_gene_variant | MODIFIER | c.-4695C>T| |
S234 |
6 | BAA05g41100 | A05 | 39427638 | C | T | upstream_gene_variant | MODIFIER | c.-4877G>A| |
S221 |