Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18130 | A10 | 17123598 | G | A | missense_variant | MODERATE | c.671C>T|p.Ala224Val |
S288 |
2 | BAA10g18130 | A10 | 17123735 | C | T | synonymous_variant | LOW | c.534G>A|p.Glu178Glu |
S299 |
3 | BAA10g18130 | A10 | 17124207 | G | A | missense_variant | MODERATE | c.62C>T|p.Ser21Leu |
S298 |
4 | BAA10g18130 | A10 | 17125981 | G | A | upstream_gene_variant | MODIFIER | c.-1713C>T| |
S35 |
5 | BAA10g18130 | A10 | 17126063 | C | T | upstream_gene_variant | MODIFIER | c.-1795G>A| |
S197 |
6 | BAA10g18130 | A10 | 17126777 | C | T | upstream_gene_variant | MODIFIER | c.-2509G>A| |
S225 S73 |