Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47450 | A09 | 51736192 | G | A | missense_variant | MODERATE | c.653C>T|p.Ala218Val |
S231 |
2 | BAA09g47450 | A09 | 51736339 | G | A | missense_variant | MODERATE | c.506C>T|p.Pro169Leu |
S134 |
3 | BAA09g47450 | A09 | 51736841 | C | T | synonymous_variant | LOW | c.231G>A|p.Leu77Leu |
S138 |
4 | BAA09g47450 | A09 | 51737840 | C | T | upstream_gene_variant | MODIFIER | c.-769G>A| |
S41 |
5 | BAA09g47450 | A09 | 51739702 | G | A | upstream_gene_variant | MODIFIER | c.-2631C>T| |
S243 |
6 | BAA09g47450 | A09 | 51741311 | G | A | upstream_gene_variant | MODIFIER | c.-4240C>T| |
S116 |