Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00100 | A04 | 35533 | C | T | missense_variant | MODERATE | c.946G>A|p.Ala316Thr |
S168 |
2 | BAA04g00100 | A04 | 37326 | G | A | missense_variant | MODERATE | c.77C>T|p.Pro26Leu |
S245 |
3 | BAA04g00100 | A04 | 37415 | C | T | upstream_gene_variant | MODIFIER | c.-13G>A| |
S174 S27 |
4 | BAA04g00100 | A04 | 42004 | C | T | upstream_gene_variant | MODIFIER | c.-4602G>A| |
S168 |
5 | BAA04g00100 | A04 | 42099 | G | A | upstream_gene_variant | MODIFIER | c.-4697C>T| |
S158 |