Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16390 | A02 | 7990121 | C | T | missense_variant | MODERATE | c.293G>A|p.Gly98Asp |
S293 |
2 | BAA02g16390 | A02 | 7990500 | C | T | missense_variant | MODERATE | c.125G>A|p.Gly42Glu |
S42 |
3 | BAA02g16390 | A02 | 7992742 | C | T | upstream_gene_variant | MODIFIER | c.-2118G>A| |
S131 |
4 | BAA02g16390 | A02 | 7994866 | G | A | upstream_gene_variant | MODIFIER | c.-4242C>T| |
S288 |
5 | BAA02g16390 | A02 | 7994970 | C | T | upstream_gene_variant | MODIFIER | c.-4346G>A| |
S273 |
6 | BAA02g16390 | A02 | 7995026 | C | T | upstream_gene_variant | MODIFIER | c.-4402G>A| |
S177 S299 |
7 | BAA02g16390 | A02 | 7995335 | G | A | upstream_gene_variant | MODIFIER | c.-4711C>T| |
S139 |