Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22980 | A02 | 12490470 | G | A | synonymous_variant | LOW | c.312C>T|p.Leu104Leu |
S132 S215 |
2 | BAA02g22980 | A02 | 12490796 | C | T | splice_region_variant&intron_variant | LOW | c.193-6G>A| |
S276 |
3 | BAA02g22980 | A02 | 12491140 | G | A | splice_region_variant&intron_variant | LOW | c.107+7C>T| |
S58 |
4 | BAA02g22980 | A02 | 12494229 | C | T | upstream_gene_variant | MODIFIER | c.-2976G>A| |
S38 |
5 | BAA02g22980 | A02 | 12496158 | G | A | upstream_gene_variant | MODIFIER | c.-4905C>T| |
S28 |