Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21300 | A02 | 11418785 | G | A | missense_variant | MODERATE | c.715C>T|p.Pro239Ser |
S238 |
2 | BAA02g21300 | A02 | 11418828 | C | T | splice_region_variant&intron_variant | LOW | c.676-4G>A| |
S25 |
3 | BAA02g21300 | A02 | 11419816 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.310-1G>A| |
S25 |
4 | BAA02g21300 | A02 | 11424820 | G | A | upstream_gene_variant | MODIFIER | c.-2280C>T| |
S279 |
5 | BAA02g21300 | A02 | 11426250 | G | A | upstream_gene_variant | MODIFIER | c.-3710C>T| |
S293 |
6 | BAA02g21300 | A02 | 11426570 | G | A | upstream_gene_variant | MODIFIER | c.-4030C>T| |
S239 |
7 | BAA02g21300 | A02 | 11426718 | G | A | upstream_gene_variant | MODIFIER | c.-4178C>T| |
S281 |