Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02900 | A02 | 1304825 | G | A | missense_variant | MODERATE | c.566C>T|p.Ser189Leu |
S136 |
2 | BAA02g02900 | A02 | 1306104 | G | A | upstream_gene_variant | MODIFIER | c.-141C>T| |
S11 |
3 | BAA02g02900 | A02 | 1306375 | G | A | upstream_gene_variant | MODIFIER | c.-412C>T| |
S203 |
4 | BAA02g02900 | A02 | 1307553 | C | T | upstream_gene_variant | MODIFIER | c.-1590G>A| |
S99 |
5 | BAA02g02900 | A02 | 1309419 | G | A | upstream_gene_variant | MODIFIER | c.-3456C>T| |
S278 |
6 | BAA02g02900 | A02 | 1309531 | C | T | upstream_gene_variant | MODIFIER | c.-3568G>A| |
S277 |
7 | BAA02g02900 | A02 | 1310604 | G | A | upstream_gene_variant | MODIFIER | c.-4641C>T| |
S158 |