Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64650 | A09 | 59901502 | C | T | missense_variant | MODERATE | c.1624G>A|p.Ala542Thr |
S163 |
2 | BAA09g64650 | A09 | 59902299 | G | A | missense_variant | MODERATE | c.1292C>T|p.Thr431Ile |
S76 |
3 | BAA09g64650 | A09 | 59902617 | C | T | missense_variant | MODERATE | c.1061G>A|p.Gly354Glu |
S50 |
4 | BAA09g64650 | A09 | 59902885 | C | T | missense_variant | MODERATE | c.793G>A|p.Asp265Asn |
S155 S211 |
5 | BAA09g64650 | A09 | 59903012 | C | T | synonymous_variant | LOW | c.666G>A|p.Gln222Gln |
S157 |