Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17960 | A02 | 9022978 | C | T | missense_variant | MODERATE | c.335C>T|p.Ser112Phe |
S32 |
2 | BAA02g17960 | A02 | 9024466 | G | A | stop_gained | HIGH | c.962G>A|p.Trp321* |
S51 |
3 | BAA02g17960 | A02 | 9024919 | G | A | missense_variant | MODERATE | c.1340G>A|p.Gly447Glu |
S159 S243 |
4 | BAA02g17960 | A02 | 9025039 | C | T | missense_variant | MODERATE | c.1460C>T|p.Thr487Ile |
S160 |
5 | BAA02g17960 | A02 | 9025422 | G | A | downstream_gene_variant | MODIFIER | c.*349G>A| |
S238 |
6 | BAA02g17960 | A02 | 9025599 | C | T | downstream_gene_variant | MODIFIER | c.*526C>T| |
S244 |
7 | BAA02g17960 | A02 | 9025941 | C | T | downstream_gene_variant | MODIFIER | c.*868C>T| |
S131 |