Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46950 | A02 | 38009979 | C | T | downstream_gene_variant | MODIFIER | c.*1665G>A| |
S121 |
2 | BAA02g46950 | A02 | 38010342 | C | T | downstream_gene_variant | MODIFIER | c.*1302G>A| |
S104 S52 |
3 | BAA02g46950 | A02 | 38011902 | C | T | synonymous_variant | LOW | c.2079G>A|p.Arg693Arg |
S260 |
4 | BAA02g46950 | A02 | 38011935 | G | A | synonymous_variant | LOW | c.2046C>T|p.Val682Val |
S152 |
5 | BAA02g46950 | A02 | 38012557 | G | A | missense_variant | MODERATE | c.1549C>T|p.Pro517Ser |
S292 |
6 | BAA02g46950 | A02 | 38012628 | G | A | missense_variant | MODERATE | c.1478C>T|p.Ala493Val |
S25 |
7 | BAA02g46950 | A02 | 38012629 | C | T | missense_variant | MODERATE | c.1477G>A|p.Ala493Thr |
S34 |
8 | BAA02g46950 | A02 | 38012848 | G | A | missense_variant | MODERATE | c.1258C>T|p.Leu420Phe |
S62 |
9 | BAA02g46950 | A02 | 38014031 | G | A | missense_variant | MODERATE | c.524C>T|p.Pro175Leu |
S221 |
10 | BAA02g46950 | A02 | 38016296 | G | A | upstream_gene_variant | MODIFIER | c.-1276C>T| |
S30 |
11 | BAA02g46950 | A02 | 38017664 | G | A | upstream_gene_variant | MODIFIER | c.-2644C>T| |
S191 |
12 | BAA02g46950 | A02 | 38017885 | G | A | upstream_gene_variant | MODIFIER | c.-2865C>T| |
S192 |
13 | BAA02g46950 | A02 | 38017938 | C | T | upstream_gene_variant | MODIFIER | c.-2918G>A| |
S61 |