Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22180 | A02 | 11943972 | C | T | missense_variant | MODERATE | c.556G>A|p.Gly186Arg |
S73 |
2 | BAA02g22180 | A02 | 11945117 | G | A | upstream_gene_variant | MODIFIER | c.-590C>T| |
S17 |
3 | BAA02g22180 | A02 | 11945969 | C | T | upstream_gene_variant | MODIFIER | c.-1442G>A| |
S181 |
4 | BAA02g22180 | A02 | 11947979 | C | T | upstream_gene_variant | MODIFIER | c.-3452G>A| |
S71 |
5 | BAA02g22180 | A02 | 11948342 | C | T | upstream_gene_variant | MODIFIER | c.-3815G>A| |
S209 |
6 | BAA02g22180 | A02 | 11948451 | T | A | upstream_gene_variant | MODIFIER | c.-3924A>T| |
S186 |
7 | BAA02g22180 | A02 | 11949093 | C | T | upstream_gene_variant | MODIFIER | c.-4566G>A| |
S178 |
8 | BAA02g22180 | A02 | 11949228 | C | T | upstream_gene_variant | MODIFIER | c.-4701G>A| |
S135 |