Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03800 | A10 | 1842228 | C | T | missense_variant | MODERATE | c.1403G>A|p.Gly468Glu |
S166 |
2 | BAA10g03800 | A10 | 1846836 | C | T | upstream_gene_variant | MODIFIER | c.-3206G>A| |
S185 |
3 | BAA10g03800 | A10 | 1848472 | C | T | upstream_gene_variant | MODIFIER | c.-4842G>A| |
S27 |
4 | BAA10g03800 | A10 | 1848532 | C | T | upstream_gene_variant | MODIFIER | c.-4902G>A| |
S197 |