Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10150 | A05 | 5158594 | C | T | missense_variant | MODERATE | c.821G>A|p.Arg274Gln |
S167 |
2 | BAA05g10150 | A05 | 5158727 | C | T | missense_variant | MODERATE | c.688G>A|p.Gly230Ser |
S28 |
3 | BAA05g10150 | A05 | 5159079 | G | A | synonymous_variant | LOW | c.336C>T|p.Phe112Phe |
S194 |
4 | BAA05g10150 | A05 | 5159087 | G | A | missense_variant | MODERATE | c.328C>T|p.Leu110Phe |
S279 |
5 | BAA05g10150 | A05 | 5159128 | G | A | missense_variant | MODERATE | c.287C>T|p.Pro96Leu |
S56 |
6 | BAA05g10150 | A05 | 5159164 | G | A | missense_variant | MODERATE | c.251C>T|p.Ala84Val |
S115 |
7 | BAA05g10150 | A05 | 5159326 | G | A | missense_variant | MODERATE | c.89C>T|p.Pro30Leu |
S239 |
8 | BAA05g10150 | A05 | 5159863 | C | T | upstream_gene_variant | MODIFIER | c.-449G>A| |
S208 S93 |
9 | BAA05g10150 | A05 | 5160648 | G | A | upstream_gene_variant | MODIFIER | c.-1234C>T| |
S157 |