Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39160 | A01 | 26038340 | G | A | missense_variant | MODERATE | c.1529C>T|p.Ser510Phe |
S152 |
2 | BAA01g39160 | A01 | 26039258 | C | T | missense_variant | MODERATE | c.853G>A|p.Ala285Thr |
S288 |
3 | BAA01g39160 | A01 | 26039843 | G | A | missense_variant | MODERATE | c.541C>T|p.Pro181Ser |
S173 |
4 | BAA01g39160 | A01 | 26039975 | G | A | missense_variant | MODERATE | c.409C>T|p.Arg137Cys |
S262 |
5 | BAA01g39160 | A01 | 26040193 | G | A | missense_variant | MODERATE | c.191C>T|p.Ser64Phe |
S160 |
6 | BAA01g39160 | A01 | 26040263 | C | T | missense_variant | MODERATE | c.121G>A|p.Ala41Thr |
S100 |
7 | BAA01g39160 | A01 | 26040326 | C | T | missense_variant | MODERATE | c.58G>A|p.Gly20Ser |
S203 |
8 | BAA01g39160 | A01 | 26040518 | C | T | upstream_gene_variant | MODIFIER | c.-48G>A| |
S302 |
9 | BAA01g39160 | A01 | 26041543 | G | A | upstream_gene_variant | MODIFIER | c.-1073C>T| |
S199 |
10 | BAA01g39160 | A01 | 26041628 | G | A | upstream_gene_variant | MODIFIER | c.-1158C>T| |
S260 |
11 | BAA01g39160 | A01 | 26045345 | G | A | upstream_gene_variant | MODIFIER | c.-4875C>T| |
S35 |