Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g01330 | A01 | 565347 | C | T | missense_variant | MODERATE | c.124C>T|p.Pro42Ser |
S184 |
2 | BAA01g01330 | A01 | 565429 | G | A | missense_variant | MODERATE | c.206G>A|p.Gly69Glu |
S212 |
3 | BAA01g01330 | A01 | 565707 | A | C | downstream_gene_variant | MODIFIER | c.*121A>C| |
S178 |
4 | BAA01g01330 | A01 | 566752 | C | T | downstream_gene_variant | MODIFIER | c.*1166C>T| |
S81 S85 |
5 | BAA01g01330 | A01 | 569434 | C | T | downstream_gene_variant | MODIFIER | c.*3848C>T| |
S236 |
6 | BAA01g01330 | A01 | 570181 | C | T | downstream_gene_variant | MODIFIER | c.*4595C>T| |
S42 |