Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42230 | A02 | 35200890 | C | T | missense_variant | MODERATE | c.791G>A|p.Ser264Asn |
S117 |
2 | BAA02g42230 | A02 | 35200893 | C | T | missense_variant | MODERATE | c.788G>A|p.Ser263Asn |
S296 |
3 | BAA02g42230 | A02 | 35201183 | C | T | synonymous_variant | LOW | c.498G>A|p.Arg166Arg |
S252 |
4 | BAA02g42230 | A02 | 35201257 | G | A | missense_variant | MODERATE | c.424C>T|p.Leu142Phe |
S60 |
5 | BAA02g42230 | A02 | 35201646 | G | A | missense_variant | MODERATE | c.35C>T|p.Ala12Val |
S125 |
6 | BAA02g42230 | A02 | 35205549 | G | A | upstream_gene_variant | MODIFIER | c.-3869C>T| |
S56 |
7 | BAA02g42230 | A02 | 35206533 | G | A | upstream_gene_variant | MODIFIER | c.-4853C>T| |
S286 |