Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19910 | A10 | 18110206 | G | A | missense_variant | MODERATE | c.347C>T|p.Ala116Val |
S162 |
2 | BAA10g19910 | A10 | 18111345 | C | T | upstream_gene_variant | MODIFIER | c.-679G>A| |
S251 |
3 | BAA10g19910 | A10 | 18113912 | C | T | upstream_gene_variant | MODIFIER | c.-3246G>A| |
S296 |
4 | BAA10g19910 | A10 | 18113914 | G | A | upstream_gene_variant | MODIFIER | c.-3248C>T| |
S69 |