Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01850 | A04 | 1072661 | C | G | missense_variant | MODERATE | c.9C>G|p.Cys3Trp |
S288 |
2 | BAA04g01850 | A04 | 1072797 | G | A | missense_variant | MODERATE | c.145G>A|p.Gly49Arg |
S128 |
3 | BAA04g01850 | A04 | 1073367 | G | A | missense_variant | MODERATE | c.715G>A|p.Val239Met |
S45 |
4 | BAA04g01850 | A04 | 1074896 | C | T | missense_variant | MODERATE | c.1625C>T|p.Ser542Phe |
S80 S98 |
5 | BAA04g01850 | A04 | 1075125 | G | A | synonymous_variant | LOW | c.1854G>A|p.Thr618Thr |
S25 |
6 | BAA04g01850 | A04 | 1078010 | G | A | downstream_gene_variant | MODIFIER | c.*2444G>A| |
S219 S72 |