Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66850 | A09 | 60882630 | C | T | missense_variant | MODERATE | c.263C>T|p.Ser88Phe |
S36 |
2 | BAA09g66850 | A09 | 60883089 | C | T | missense_variant | MODERATE | c.722C>T|p.Ala241Val |
S219 S72 |
3 | BAA09g66850 | A09 | 60884653 | G | A | missense_variant | MODERATE | c.1577G>A|p.Gly526Glu |
S189 |
4 | BAA09g66850 | A09 | 60884654 | G | A | synonymous_variant | LOW | c.1578G>A|p.Gly526Gly |
S166 |
5 | BAA09g66850 | A09 | 60884773 | G | A | missense_variant | MODERATE | c.1697G>A|p.Gly566Asp |
S79 S84 |
6 | BAA09g66850 | A09 | 60885129 | G | A | missense_variant | MODERATE | c.2053G>A|p.Asp685Asn |
S283 |
7 | BAA09g66850 | A09 | 60885286 | G | A | missense_variant | MODERATE | c.2210G>A|p.Arg737Lys |
S186 |
8 | BAA09g66850 | A09 | 60885290 | C | T | synonymous_variant | LOW | c.2214C>T|p.Leu738Leu |
S171 |