Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00870 | A02 | 410166 | G | A | missense_variant | MODERATE | c.809C>T|p.Thr270Ile |
S296 |
2 | BAA02g00870 | A02 | 410617 | G | A | stop_gained | HIGH | c.538C>T|p.Gln180* |
S210 S225 |
3 | BAA02g00870 | A02 | 410920 | C | T | synonymous_variant | LOW | c.324G>A|p.Gln108Gln |
S257 |
4 | BAA02g00870 | A02 | 411385 | C | T | missense_variant | MODERATE | c.76G>A|p.Ala26Thr |
S180 |
5 | BAA02g00870 | A02 | 414830 | C | T | upstream_gene_variant | MODIFIER | c.-3370G>A| |
S277 |
6 | BAA02g00870 | A02 | 415236 | G | A | upstream_gene_variant | MODIFIER | c.-3776C>T| |
S109 |
7 | BAA02g00870 | A02 | 415655 | G | A | upstream_gene_variant | MODIFIER | c.-4195C>T| |
S190 |