Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06020 | A02 | 2555937 | C | T | splice_region_variant&synonymous_variant | LOW | c.1440G>A|p.Glu480Glu |
S293 |
2 | BAA02g06020 | A02 | 2556072 | G | A | synonymous_variant | LOW | c.1305C>T|p.Thr435Thr |
S203 |
3 | BAA02g06020 | A02 | 2557324 | G | A | missense_variant | MODERATE | c.703C>T|p.Pro235Ser |
S279 |
4 | BAA02g06020 | A02 | 2557530 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.594-1G>A| |
S81 S85 |
5 | BAA02g06020 | A02 | 2558103 | G | A | missense_variant | MODERATE | c.403C>T|p.His135Tyr |
S62 |
6 | BAA02g06020 | A02 | 2558816 | G | A | upstream_gene_variant | MODIFIER | c.-195C>T| |
S51 |
7 | BAA02g06020 | A02 | 2562546 | C | T | upstream_gene_variant | MODIFIER | c.-3925G>A| |
S295 |
8 | BAA02g06020 | A02 | 2562768 | G | A | upstream_gene_variant | MODIFIER | c.-4147C>T| |
S205 |
9 | BAA02g06020 | A02 | 2563613 | G | A | upstream_gene_variant | MODIFIER | c.-4992C>T| |
S291 |