Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18000 | A01 | 8807210 | C | T | missense_variant | MODERATE | c.1357G>A|p.Asp453Asn |
S155 S211 |
2 | BAA01g18000 | A01 | 8807296 | G | A | missense_variant | MODERATE | c.1271C>T|p.Pro424Leu |
S159 S243 |
3 | BAA01g18000 | A01 | 8807767 | C | T | missense_variant | MODERATE | c.980G>A|p.Arg327Lys |
S185 |
4 | BAA01g18000 | A01 | 8807900 | G | A | missense_variant | MODERATE | c.914C>T|p.Ser305Phe |
S239 |
5 | BAA01g18000 | A01 | 8808962 | G | A | missense_variant | MODERATE | c.385C>T|p.Leu129Phe |
S152 |
6 | BAA01g18000 | A01 | 8813037 | C | T | upstream_gene_variant | MODIFIER | c.-3259G>A| |
S99 |
7 | BAA01g18000 | A01 | 8813225 | C | T | upstream_gene_variant | MODIFIER | c.-3447G>A| |
S170 |
8 | BAA01g18000 | A01 | 8813329 | G | A | upstream_gene_variant | MODIFIER | c.-3551C>T| |
S298 |
9 | BAA01g18000 | A01 | 8814495 | G | A | upstream_gene_variant | MODIFIER | c.-4717C>T| |
S131 |