Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45160 | A02 | 37051639 | C | T | missense_variant | MODERATE | c.142G>A|p.Asp48Asn |
S112 |
2 | BAA02g45160 | A02 | 37053499 | G | A | upstream_gene_variant | MODIFIER | c.-1615C>T| |
S81 S85 |
3 | BAA02g45160 | A02 | 37053653 | C | T | upstream_gene_variant | MODIFIER | c.-1769G>A| |
S123 |
4 | BAA02g45160 | A02 | 37056175 | G | A | upstream_gene_variant | MODIFIER | c.-4291C>T| |
S62 |
5 | BAA02g45160 | A02 | 37056353 | C | T | upstream_gene_variant | MODIFIER | c.-4469G>A| |
S173 |