Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20970 | A02 | 11181755 | G | A | missense_variant | MODERATE | c.185C>T|p.Thr62Met |
S57 |
2 | BAA02g20970 | A02 | 11182105 | G | A | upstream_gene_variant | MODIFIER | c.-166C>T| |
S45 |
3 | BAA02g20970 | A02 | 11182985 | G | A | upstream_gene_variant | MODIFIER | c.-1046C>T| |
S161 |
4 | BAA02g20970 | A02 | 11183893 | C | T | upstream_gene_variant | MODIFIER | c.-1954G>A| |
S46 |
5 | BAA02g20970 | A02 | 11184100 | G | A | upstream_gene_variant | MODIFIER | c.-2161C>T| |
S44 |
6 | BAA02g20970 | A02 | 11184197 | C | T | upstream_gene_variant | MODIFIER | c.-2258G>A| |
S284 |
7 | BAA02g20970 | A02 | 11184233 | C | T | upstream_gene_variant | MODIFIER | c.-2294G>A| |
S268 |
8 | BAA02g20970 | A02 | 11185127 | G | A | upstream_gene_variant | MODIFIER | c.-3188C>T| |
S247 |
9 | BAA02g20970 | A02 | 11185219 | G | A | upstream_gene_variant | MODIFIER | c.-3280C>T| |
S237 |