Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g38400 | A03 | 17785219 | C | T | upstream_gene_variant | MODIFIER | c.-4117C>T| |
S172 S217 |
2 | BAA03g38400 | A03 | 17785431 | G | A | upstream_gene_variant | MODIFIER | c.-3905G>A| |
S56 |
3 | BAA03g38400 | A03 | 17786836 | C | T | upstream_gene_variant | MODIFIER | c.-2500C>T| |
S211 |
4 | BAA03g38400 | A03 | 17787169 | G | A | upstream_gene_variant | MODIFIER | c.-2167G>A| |
S71 |
5 | BAA03g38400 | A03 | 17790648 | G | A | synonymous_variant | LOW | c.708G>A|p.Glu236Glu |
S265 |
6 | BAA03g38400 | A03 | 17790800 | G | A | missense_variant | MODERATE | c.860G>A|p.Gly287Asp |
S189 |
7 | BAA03g38400 | A03 | 17792133 | G | A | missense_variant | MODERATE | c.1642G>A|p.Glu548Lys |
S149 |
8 | BAA03g38400 | A03 | 17792346 | G | A | missense_variant | MODERATE | c.1855G>A|p.Glu619Lys |
S277 |
9 | BAA03g38400 | A03 | 17792467 | C | T | missense_variant | MODERATE | c.1976C>T|p.Thr659Ile |
S34 |