Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g02020 | A09 | 1400523 | C | T | missense_variant | MODERATE | c.1328G>A|p.Gly443Glu |
S115 |
2 | BAA09g02020 | A09 | 1401317 | G | A | synonymous_variant | LOW | c.534C>T|p.Phe178Phe |
S57 |
3 | BAA09g02020 | A09 | 1401658 | G | A | missense_variant | MODERATE | c.193C>T|p.Leu65Phe |
S53 |
4 | BAA09g02020 | A09 | 1401751 | G | A | missense_variant | MODERATE | c.100C>T|p.Pro34Ser |
S265 |
5 | BAA09g02020 | A09 | 1401772 | C | T | missense_variant | MODERATE | c.79G>A|p.Asp27Asn |
S64 |