Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20620 | A02 | 10927824 | C | T | missense_variant | MODERATE | c.1144G>A|p.Glu382Lys |
S160 |
2 | BAA02g20620 | A02 | 10927966 | C | T | stop_gained | HIGH | c.1002G>A|p.Trp334* |
S35 |
3 | BAA02g20620 | A02 | 10928439 | G | A | missense_variant | MODERATE | c.695C>T|p.Ala232Val |
S10 S33 |
4 | BAA02g20620 | A02 | 10929024 | C | T | missense_variant | MODERATE | c.523G>A|p.Ala175Thr |
S51 |
5 | BAA02g20620 | A02 | 10929043 | G | A | synonymous_variant | LOW | c.504C>T|p.His168His |
S10 |
6 | BAA02g20620 | A02 | 10929488 | G | A | synonymous_variant | LOW | c.303C>T|p.Phe101Phe |
S278 |
7 | BAA02g20620 | A02 | 10929851 | G | A | synonymous_variant | LOW | c.126C>T|p.Arg42Arg |
S303 |
8 | BAA02g20620 | A02 | 10935857 | C | T | upstream_gene_variant | MODIFIER | c.-4238G>A| |
S201 |