Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g12690 | A09 | 7305802 | G | A | upstream_gene_variant | MODIFIER | c.-13G>A| |
S184 |
2 | BAA09g12690 | A09 | 7306259 | G | A | synonymous_variant | LOW | c.231G>A|p.Leu77Leu |
S180 |
3 | BAA09g12690 | A09 | 7306696 | G | A | missense_variant | MODERATE | c.488G>A|p.Gly163Glu |
S113 |
4 | BAA09g12690 | A09 | 7307776 | C | T | missense_variant | MODERATE | c.1127C>T|p.Ser376Phe |
S158 |
5 | BAA09g12690 | A09 | 7308008 | C | T | missense_variant | MODERATE | c.1262C>T|p.Pro421Leu |
S213 |
6 | BAA09g12690 | A09 | 7310593 | C | T | downstream_gene_variant | MODIFIER | c.*2341C>T| |
S295 |
7 | BAA09g12690 | A09 | 7311216 | G | A | downstream_gene_variant | MODIFIER | c.*2964G>A| |
S1 S90 |
8 | BAA09g12690 | A09 | 7311741 | C | T | downstream_gene_variant | MODIFIER | c.*3489C>T| |
S182 |
9 | BAA09g12690 | A09 | 7312919 | G | A | downstream_gene_variant | MODIFIER | c.*4667G>A| |
S79 |