Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g21790 | A09 | 13599703 | G | A | missense_variant | MODERATE | c.982C>T|p.Pro328Ser |
S138 |
2 | BAA09g21790 | A09 | 13600659 | C | T | missense_variant | MODERATE | c.454G>A|p.Gly152Ser |
S231 |
3 | BAA09g21790 | A09 | 13601266 | G | A | missense_variant | MODERATE | c.92C>T|p.Thr31Met |
S226 |
4 | BAA09g21790 | A09 | 13602543 | G | A | upstream_gene_variant | MODIFIER | c.-1186C>T| |
S66 |
5 | BAA09g21790 | A09 | 13603233 | G | A | upstream_gene_variant | MODIFIER | c.-1876C>T| |
S201 |
6 | BAA09g21790 | A09 | 13603399 | C | T | upstream_gene_variant | MODIFIER | c.-2042G>A| |
S96 |
7 | BAA09g21790 | A09 | 13603658 | G | A | upstream_gene_variant | MODIFIER | c.-2301C>T| |
S130 |
8 | BAA09g21790 | A09 | 13605358 | C | T | upstream_gene_variant | MODIFIER | c.-4001G>A| |
S109 |