Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10360 | A01 | 4731188 | C | T | missense_variant | MODERATE | c.62C>T|p.Ser21Phe |
S109 |
2 | BAA01g10360 | A01 | 4732845 | G | A | intron_variant | MODIFIER | c.846+22G>A| |
S238 |
3 | BAA01g10360 | A01 | 4733116 | C | T | synonymous_variant | LOW | c.990C>T|p.Ser330Ser |
S182 |
4 | BAA01g10360 | A01 | 4733245 | C | T | intron_variant | MODIFIER | c.1077+42C>T| |
S150 |