Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40620 | A02 | 34184853 | C | T | missense_variant&splice_region_variant | MODERATE | c.284G>A|p.Gly95Glu |
S100 |
2 | BAA02g40620 | A02 | 34185703 | G | A | missense_variant | MODERATE | c.259C>T|p.Leu87Phe |
S168 |
3 | BAA02g40620 | A02 | 34185922 | C | T | missense_variant | MODERATE | c.40G>A|p.Gly14Arg |
S273 |
4 | BAA02g40620 | A02 | 34189863 | C | T | upstream_gene_variant | MODIFIER | c.-3902G>A| |
S40 S49 |
5 | BAA02g40620 | A02 | 34190032 | G | A | upstream_gene_variant | MODIFIER | c.-4071C>T| |
S282 |
6 | BAA02g40620 | A02 | 34190454 | G | A | upstream_gene_variant | MODIFIER | c.-4493C>T| |
S143 |