Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00200 | A09 | 337173 | C | T | missense_variant | MODERATE | c.37C>T|p.Leu13Phe |
S149 |
2 | BAA09g00200 | A09 | 338316 | G | A | missense_variant | MODERATE | c.626G>A|p.Arg209Gln |
S30 S31 |
3 | BAA09g00200 | A09 | 339107 | C | T | missense_variant | MODERATE | c.1265C>T|p.Thr422Ile |
S53 |
4 | BAA09g00200 | A09 | 339541 | C | T | missense_variant | MODERATE | c.1528C>T|p.Pro510Ser |
S189 |
5 | BAA09g00200 | A09 | 339985 | C | T | missense_variant | MODERATE | c.1906C>T|p.Arg636Cys |
S200 |
6 | BAA09g00200 | A09 | 340013 | C | T | missense_variant | MODERATE | c.1934C>T|p.Pro645Leu |
S206 |