Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08910 | A02 | 3942904 | G | A | synonymous_variant | LOW | c.1671C>T|p.Asn557Asn |
S197 |
2 | BAA02g08910 | A02 | 3943595 | G | A | missense_variant | MODERATE | c.980C>T|p.Ala327Val |
S289 S290 |
3 | BAA02g08910 | A02 | 3944036 | C | T | missense_variant | MODERATE | c.539G>A|p.Ser180Asn |
S262 |
4 | BAA02g08910 | A02 | 3944144 | G | A | missense_variant | MODERATE | c.431C>T|p.Thr144Ile |
S161 |
5 | BAA02g08910 | A02 | 3944583 | G | A | missense_variant | MODERATE | c.233C>T|p.Ala78Val |
S82 S92 |
6 | BAA02g08910 | A02 | 3944881 | G | A | upstream_gene_variant | MODIFIER | c.-66C>T| |
S110 |
7 | BAA02g08910 | A02 | 3945045 | G | A | upstream_gene_variant | MODIFIER | c.-230C>T| |
S165 |
8 | BAA02g08910 | A02 | 3945747 | G | A | upstream_gene_variant | MODIFIER | c.-932C>T| |
S177 |
9 | BAA02g08910 | A02 | 3947466 | G | A | upstream_gene_variant | MODIFIER | c.-2651C>T| |
S69 |
10 | BAA02g08910 | A02 | 3949101 | C | T | upstream_gene_variant | MODIFIER | c.-4286G>A| |
S268 |
11 | BAA02g08910 | A02 | 3949575 | G | A | upstream_gene_variant | MODIFIER | c.-4760C>T| |
S303 |