Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34090 | A02 | 29220178 | C | T | missense_variant | MODERATE | c.1106G>A|p.Gly369Glu |
S135 S185 S203 S273 |
2 | BAA02g34090 | A02 | 29220615 | G | A | synonymous_variant | LOW | c.669C>T|p.Leu223Leu |
S45 |
3 | BAA02g34090 | A02 | 29220767 | G | A | missense_variant | MODERATE | c.517C>T|p.Leu173Phe |
S199 |
4 | BAA02g34090 | A02 | 29222058 | G | A | missense_variant | MODERATE | c.218C>T|p.Thr73Ile |
S34 |
5 | BAA02g34090 | A02 | 29224415 | G | A | upstream_gene_variant | MODIFIER | c.-2140C>T| |
S143 |
6 | BAA02g34090 | A02 | 29224614 | G | A | upstream_gene_variant | MODIFIER | c.-2339C>T| |
S271 |
7 | BAA02g34090 | A02 | 29226446 | G | A | upstream_gene_variant | MODIFIER | c.-4171C>T| |
S204 |
8 | BAA02g34090 | A02 | 29226531 | C | T | upstream_gene_variant | MODIFIER | c.-4256G>A| |
S296 |