Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04690 | A02 | 2033854 | C | T | missense_variant | MODERATE | c.350C>T|p.Ala117Val |
S181 |
2 | BAA02g04690 | A02 | 2033944 | C | T | missense_variant | MODERATE | c.440C>T|p.Ser147Phe |
S111 |
3 | BAA02g04690 | A02 | 2035848 | G | A | synonymous_variant | LOW | c.522G>A|p.Ser174Ser |
S48 |
4 | BAA02g04690 | A02 | 2037328 | C | T | synonymous_variant | LOW | c.1090C>T|p.Leu364Leu |
S152 |
5 | BAA02g04690 | A02 | 2039202 | C | T | downstream_gene_variant | MODIFIER | c.*1593C>T| |
S252 |
6 | BAA02g04690 | A02 | 2040230 | C | T | downstream_gene_variant | MODIFIER | c.*2621C>T| |
S19 |