Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11390 | A09 | 6385000 | G | A | upstream_gene_variant | MODIFIER | c.-4618G>A| |
S20 |
2 | BAA09g11390 | A09 | 6390224 | C | T | missense_variant | MODERATE | c.485C>T|p.Ser162Phe |
S263 |
3 | BAA09g11390 | A09 | 6390242 | C | T | missense_variant | MODERATE | c.503C>T|p.Ala168Val |
S263 |
4 | BAA09g11390 | A09 | 6390619 | C | T | missense_variant | MODERATE | c.880C>T|p.Leu294Phe |
S104 S52 |
5 | BAA09g11390 | A09 | 6392838 | C | T | downstream_gene_variant | MODIFIER | c.*1998C>T| |
S281 |
6 | BAA09g11390 | A09 | 6393464 | C | T | downstream_gene_variant | MODIFIER | c.*2624C>T| |
S135 |
7 | BAA09g11390 | A09 | 6393816 | C | T | downstream_gene_variant | MODIFIER | c.*2976C>T| |
S216 |