Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00440 | A09 | 476572 | G | A | missense_variant | MODERATE | c.89C>T|p.Ala30Val |
S295 |
2 | BAA09g00440 | A09 | 476704 | G | A | upstream_gene_variant | MODIFIER | c.-44C>T| |
S170 |
3 | BAA09g00440 | A09 | 476740 | G | A | upstream_gene_variant | MODIFIER | c.-80C>T| |
S283 |
4 | BAA09g00440 | A09 | 477662 | G | A | upstream_gene_variant | MODIFIER | c.-1002C>T| |
S295 |
5 | BAA09g00440 | A09 | 480825 | C | T | upstream_gene_variant | MODIFIER | c.-4165G>A| |
S25 S264 |
6 | BAA09g00440 | A09 | 481285 | C | T | upstream_gene_variant | MODIFIER | c.-4625G>A| |
S64 |