Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35990 | A02 | 30971607 | G | A | synonymous_variant | LOW | c.660C>T|p.Asp220Asp |
S111 |
2 | BAA02g35990 | A02 | 30971747 | C | T | missense_variant | MODERATE | c.520G>A|p.Gly174Arg |
S255 |
3 | BAA02g35990 | A02 | 30971757 | C | T | synonymous_variant | LOW | c.510G>A|p.Pro170Pro |
S206 |
4 | BAA02g35990 | A02 | 30974500 | G | A | upstream_gene_variant | MODIFIER | c.-1989C>T| |
S186 |
5 | BAA02g35990 | A02 | 30977363 | C | T | upstream_gene_variant | MODIFIER | c.-4852G>A| |
S15 S3 |