Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19770 | A02 | 10331162 | C | T | upstream_gene_variant | MODIFIER | c.-1669C>T| |
S261 |
2 | BAA02g19770 | A02 | 10331372 | C | T | upstream_gene_variant | MODIFIER | c.-1459C>T| |
S221 |
3 | BAA02g19770 | A02 | 10332906 | G | A | missense_variant | MODERATE | c.76G>A|p.Glu26Lys |
S50 |
4 | BAA02g19770 | A02 | 10334564 | G | A | downstream_gene_variant | MODIFIER | c.*1491G>A| |
S150 |
5 | BAA02g19770 | A02 | 10334659 | G | A | downstream_gene_variant | MODIFIER | c.*1586G>A| |
S150 |
6 | BAA02g19770 | A02 | 10336078 | G | A | downstream_gene_variant | MODIFIER | c.*3005G>A| |
S69 |