Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04770 | A02 | 2072203 | G | A | missense_variant | MODERATE | c.1196C>T|p.Ala399Val |
S122 |
2 | BAA02g04770 | A02 | 2073480 | G | A | synonymous_variant | LOW | c.792C>T|p.Ile264Ile |
S238 |
3 | BAA02g04770 | A02 | 2074450 | G | A | missense_variant | MODERATE | c.659C>T|p.Ser220Phe |
S217 |
4 | BAA02g04770 | A02 | 2074506 | G | A | synonymous_variant | LOW | c.603C>T|p.Phe201Phe |
S34 |
5 | BAA02g04770 | A02 | 2074938 | G | A | synonymous_variant | LOW | c.243C>T|p.Phe81Phe |
S63 |
6 | BAA02g04770 | A02 | 2076085 | C | T | synonymous_variant | LOW | c.135G>A|p.Glu45Glu |
S15 |
7 | BAA02g04770 | A02 | 2077082 | C | T | upstream_gene_variant | MODIFIER | c.-863G>A| |
S181 |
8 | BAA02g04770 | A02 | 2077573 | C | T | upstream_gene_variant | MODIFIER | c.-1354G>A| |
S104 |