Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37360 | A02 | 32014686 | G | A | missense_variant | MODERATE | c.184G>A|p.Ala62Thr |
S298 |
2 | BAA02g37360 | A02 | 32014766 | G | A | splice_region_variant&intron_variant | LOW | c.261+3G>A| |
S144 |
3 | BAA02g37360 | A02 | 32014959 | C | T | synonymous_variant | LOW | c.390C>T|p.Ala130Ala |
S2 S4 S6 |
4 | BAA02g37360 | A02 | 32015525 | C | T | synonymous_variant | LOW | c.807C>T|p.Ile269Ile |
S252 |