Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02020 | A02 | 896889 | C | T | upstream_gene_variant | MODIFIER | c.-1494C>T| |
S200 |
2 | BAA02g02020 | A02 | 898491 | C | T | missense_variant | MODERATE | c.109C>T|p.Pro37Ser |
S34 |
3 | BAA02g02020 | A02 | 899714 | G | A | missense_variant&splice_region_variant | MODERATE | c.529G>A|p.Val177Ile |
S169 |