Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00380 | A02 | 212901 | C | T | missense_variant | MODERATE | c.394G>A|p.Gly132Arg |
S32 |
2 | BAA02g00380 | A02 | 213302 | C | T | missense_variant | MODERATE | c.178G>A|p.Gly60Ser |
S251 |
3 | BAA02g00380 | A02 | 214141 | G | A | upstream_gene_variant | MODIFIER | c.-491C>T| |
S265 |
4 | BAA02g00380 | A02 | 215237 | G | A | upstream_gene_variant | MODIFIER | c.-1587C>T| |
S98 |
5 | BAA02g00380 | A02 | 215674 | C | T | upstream_gene_variant | MODIFIER | c.-2024G>A| |
S221 |
6 | BAA02g00380 | A02 | 216830 | G | A | upstream_gene_variant | MODIFIER | c.-3180C>T| |
S50 |