Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26860 | A02 | 15047345 | C | T | missense_variant | MODERATE | c.1130G>A|p.Arg377Lys |
S170 |
2 | BAA02g26860 | A02 | 15047387 | C | T | missense_variant | MODERATE | c.1088G>A|p.Gly363Glu |
S140 |
3 | BAA02g26860 | A02 | 15048404 | C | T | missense_variant | MODERATE | c.683G>A|p.Gly228Glu |
S107 |
4 | BAA02g26860 | A02 | 15048408 | G | A | missense_variant | MODERATE | c.679C>T|p.Leu227Phe |
S279 |
5 | BAA02g26860 | A02 | 15048873 | C | T | missense_variant | MODERATE | c.214G>A|p.Gly72Arg |
S9 |
6 | BAA02g26860 | A02 | 15049012 | G | A | synonymous_variant | LOW | c.75C>T|p.Pro25Pro |
S62 |
7 | BAA02g26860 | A02 | 15051913 | C | T | upstream_gene_variant | MODIFIER | c.-2827G>A| |
S246 |