Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46650 | A01 | 31052378 | C | T | upstream_gene_variant | MODIFIER | c.-218C>T| |
S108 |
2 | BAA01g46650 | A01 | 31054292 | C | T | missense_variant | MODERATE | c.1564C>T|p.Pro522Ser |
S91 |
3 | BAA01g46650 | A01 | 31054332 | C | T | missense_variant | MODERATE | c.1604C>T|p.Pro535Leu |
S99 |
4 | BAA01g46650 | A01 | 31056583 | G | A | downstream_gene_variant | MODIFIER | c.*2004G>A| |
S63 |