Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19760 | A02 | 10323893 | G | A | missense_variant | MODERATE | c.316C>T|p.Pro106Ser |
S166 |
2 | BAA02g19760 | A02 | 10324066 | C | T | synonymous_variant | LOW | c.255G>A|p.Arg85Arg |
S32 |
3 | BAA02g19760 | A02 | 10324236 | C | T | intron_variant | MODIFIER | c.205+83G>A| |
S103 |
4 | BAA02g19760 | A02 | 10326944 | C | T | upstream_gene_variant | MODIFIER | c.-2421G>A| |
S281 |
5 | BAA02g19760 | A02 | 10326962 | G | A | upstream_gene_variant | MODIFIER | c.-2439C>T| |
S287 |
6 | BAA02g19760 | A02 | 10327626 | C | G | upstream_gene_variant | MODIFIER | c.-3103G>C| |
S6 |
7 | BAA02g19760 | A02 | 10328497 | C | T | upstream_gene_variant | MODIFIER | c.-3974G>A| |
S268 |