Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g02190 | A08 | 1564857 | C | T | missense_variant | MODERATE | c.227C>T|p.Thr76Ile |
S215 |
2 | BAA08g02190 | A08 | 1568037 | G | A | downstream_gene_variant | MODIFIER | c.*3017G>A| |
S48 |
3 | BAA08g02190 | A08 | 1568071 | C | T | downstream_gene_variant | MODIFIER | c.*3051C>T| |
S149 |