Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18100 | A02 | 9096724 | C | T | missense_variant | MODERATE | c.286G>A|p.Ala96Thr |
S5 |
2 | BAA02g18100 | A02 | 9096964 | C | T | missense_variant | MODERATE | c.46G>A|p.Glu16Lys |
S242 |
3 | BAA02g18100 | A02 | 9097908 | C | T | upstream_gene_variant | MODIFIER | c.-899G>A| |
S262 |
4 | BAA02g18100 | A02 | 9098161 | G | A | upstream_gene_variant | MODIFIER | c.-1152C>T| |
S272 |
5 | BAA02g18100 | A02 | 9098206 | G | A | upstream_gene_variant | MODIFIER | c.-1197C>T| |
S133 |
6 | BAA02g18100 | A02 | 9098207 | C | T | upstream_gene_variant | MODIFIER | c.-1198G>A| |
S283 |
7 | BAA02g18100 | A02 | 9099336 | C | T | upstream_gene_variant | MODIFIER | c.-2327G>A| |
S210 |