Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09060 | A01 | 3976383 | C | T | missense_variant | MODERATE | c.676G>A|p.Asp226Asn |
S38 |
2 | BAA01g09060 | A01 | 3977014 | G | A | missense_variant | MODERATE | c.149C>T|p.Ser50Phe |
S162 |
3 | BAA01g09060 | A01 | 3979003 | G | A | upstream_gene_variant | MODIFIER | c.-1841C>T| |
S63 |
4 | BAA01g09060 | A01 | 3981336 | C | T | upstream_gene_variant | MODIFIER | c.-4174G>A| |
S54 |