Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15830 | A10 | 16017349 | G | A | missense_variant | MODERATE | c.1879C>T|p.Pro627Ser |
S158 |
2 | BAA10g15830 | A10 | 16017685 | G | A | synonymous_variant | LOW | c.1543C>T|p.Leu515Leu |
S273 |
3 | BAA10g15830 | A10 | 16018572 | G | A | missense_variant | MODERATE | c.887C>T|p.Ser296Phe |
S120 |
4 | BAA10g15830 | A10 | 16018665 | C | T | stop_gained | HIGH | c.794G>A|p.Trp265* |
S246 |
5 | BAA10g15830 | A10 | 16018881 | C | T | missense_variant | MODERATE | c.578G>A|p.Gly193Glu |
S306 S308 |
6 | BAA10g15830 | A10 | 16024243 | G | A | upstream_gene_variant | MODIFIER | c.-3782C>T| |
S261 |
7 | BAA10g15830 | A10 | 16024306 | G | A | upstream_gene_variant | MODIFIER | c.-3845C>T| |
S129 |
8 | BAA10g15830 | A10 | 16024425 | G | A | upstream_gene_variant | MODIFIER | c.-3964C>T| |
S125 |
9 | BAA10g15830 | A10 | 16024513 | G | T | upstream_gene_variant | MODIFIER | c.-4052C>A| |
S53 |