Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42130 | A02 | 35122528 | G | A | missense_variant | MODERATE | c.1351C>T|p.Leu451Phe |
S286 |
2 | BAA02g42130 | A02 | 35122865 | G | A | synonymous_variant | LOW | c.1014C>T|p.Asn338Asn |
S223 |
3 | BAA02g42130 | A02 | 35123926 | G | A | synonymous_variant | LOW | c.609C>T|p.Leu203Leu |
S81 S85 |
4 | BAA02g42130 | A02 | 35124190 | C | T | synonymous_variant | LOW | c.417G>A|p.Arg139Arg |
S135 S57 |
5 | BAA02g42130 | A02 | 35124267 | C | T | missense_variant | MODERATE | c.340G>A|p.Gly114Ser |
S224 |
6 | BAA02g42130 | A02 | 35124419 | G | A | missense_variant | MODERATE | c.188C>T|p.Ser63Leu |
S168 |
7 | BAA02g42130 | A02 | 35124553 | C | T | synonymous_variant | LOW | c.54G>A|p.Gln18Gln |
S173 |
8 | BAA02g42130 | A02 | 35125265 | G | A | upstream_gene_variant | MODIFIER | c.-659C>T| |
S110 |
9 | BAA02g42130 | A02 | 35127855 | C | T | upstream_gene_variant | MODIFIER | c.-3249G>A| |
S40 S49 |
10 | BAA02g42130 | A02 | 35128862 | C | T | upstream_gene_variant | MODIFIER | c.-4256G>A| |
S139 |