Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15500 | A01 | 7483552 | C | T | missense_variant | MODERATE | c.1967G>A|p.Arg656Lys |
S1 |
2 | BAA01g15500 | A01 | 7483910 | G | A | missense_variant | MODERATE | c.1609C>T|p.Leu537Phe |
S40 |
3 | BAA01g15500 | A01 | 7484023 | G | T | missense_variant | MODERATE | c.1496C>A|p.Pro499His |
S237 |
4 | BAA01g15500 | A01 | 7485905 | C | T | synonymous_variant | LOW | c.444G>A|p.Leu148Leu |
S148 |
5 | BAA01g15500 | A01 | 7487144 | G | A | upstream_gene_variant | MODIFIER | c.-505C>T| |
S56 |
6 | BAA01g15500 | A01 | 7490781 | C | T | upstream_gene_variant | MODIFIER | c.-4142G>A| |
S71 |
7 | BAA01g15500 | A01 | 7491460 | G | A | upstream_gene_variant | MODIFIER | c.-4821C>T| |
S74 |