Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g06850 | A09 | 3810345 | C | T | missense_variant | MODERATE | c.1486G>A|p.Glu496Lys |
S173 |
2 | BAA09g06850 | A09 | 3810755 | C | T | missense_variant | MODERATE | c.1256G>A|p.Ser419Asn |
S263 |
3 | BAA09g06850 | A09 | 3811322 | C | T | missense_variant | MODERATE | c.754G>A|p.Asp252Asn |
S277 |
4 | BAA09g06850 | A09 | 3811397 | C | T | missense_variant | MODERATE | c.679G>A|p.Asp227Asn |
S183 S198 |
5 | BAA09g06850 | A09 | 3811451 | C | T | missense_variant | MODERATE | c.625G>A|p.Val209Ile |
S210 S225 |
6 | BAA09g06850 | A09 | 3812540 | G | A | missense_variant | MODERATE | c.62C>T|p.Ser21Phe |
S226 |
7 | BAA09g06850 | A09 | 3812591 | G | A | missense_variant | MODERATE | c.11C>T|p.Ala4Val |
S277 |
8 | BAA09g06850 | A09 | 3812858 | G | A | upstream_gene_variant | MODIFIER | c.-257C>T| |
S277 |
9 | BAA09g06850 | A09 | 3814445 | C | T | upstream_gene_variant | MODIFIER | c.-1844G>A| |
S244 |
10 | BAA09g06850 | A09 | 3814499 | C | T | upstream_gene_variant | MODIFIER | c.-1898G>A| |
S50 |