Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17680 | A02 | 8805590 | C | T | missense_variant | MODERATE | c.2855G>A|p.Gly952Glu |
S175 |
2 | BAA02g17680 | A02 | 8806352 | C | T | missense_variant | MODERATE | c.2365G>A|p.Glu789Lys |
S123 |
3 | BAA02g17680 | A02 | 8807060 | G | A | missense_variant | MODERATE | c.2002C>T|p.Leu668Phe |
S197 |
4 | BAA02g17680 | A02 | 8807403 | G | A | synonymous_variant | LOW | c.1729C>T|p.Leu577Leu |
S237 |
5 | BAA02g17680 | A02 | 8807911 | C | T | synonymous_variant | LOW | c.1221G>A|p.Arg407Arg |
S212 |
6 | BAA02g17680 | A02 | 8808419 | C | T | missense_variant | MODERATE | c.713G>A|p.Arg238Gln |
S179 |
7 | BAA02g17680 | A02 | 8808489 | C | T | missense_variant | MODERATE | c.643G>A|p.Gly215Arg |
S255 |
8 | BAA02g17680 | A02 | 8809905 | G | A | upstream_gene_variant | MODIFIER | c.-774C>T| |
S256 |
9 | BAA02g17680 | A02 | 8809906 | C | T | upstream_gene_variant | MODIFIER | c.-775G>A| |
S182 |
10 | BAA02g17680 | A02 | 8811714 | C | T | upstream_gene_variant | MODIFIER | c.-2583G>A| |
S271 |
11 | BAA02g17680 | A02 | 8812696 | C | T | upstream_gene_variant | MODIFIER | c.-3565G>A| |
S32 |