Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25670 | A02 | 14087551 | G | A | missense_variant | MODERATE | c.517G>A|p.Val173Ile |
S288 |
2 | BAA02g25670 | A02 | 14088017 | G | A | missense_variant | MODERATE | c.983G>A|p.Gly328Asp |
S128 |
3 | BAA02g25670 | A02 | 14088100 | C | T | missense_variant | MODERATE | c.1066C>T|p.Pro356Ser |
S292 |
4 | BAA02g25670 | A02 | 14089795 | C | T | synonymous_variant | LOW | c.1812C>T|p.Asn604Asn |
S171 |
5 | BAA02g25670 | A02 | 14092355 | G | A | synonymous_variant | LOW | c.2946G>A|p.Leu982Leu |
S23 |
6 | BAA02g25670 | A02 | 14092945 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.3050-1G>A| |
S45 |