Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g17400 | A01 | 8456313 | C | T | missense_variant | MODERATE | c.1223G>A|p.Arg408Lys |
S295 |
2 | BAA01g17400 | A01 | 8456470 | C | T | missense_variant | MODERATE | c.1150G>A|p.Ala384Thr |
S18 |
3 | BAA01g17400 | A01 | 8456752 | C | T | missense_variant | MODERATE | c.868G>A|p.Glu290Lys |
S117 |
4 | BAA01g17400 | A01 | 8457253 | C | T | missense_variant | MODERATE | c.367G>A|p.Glu123Lys |
S50 |
5 | BAA01g17400 | A01 | 8457445 | C | T | missense_variant | MODERATE | c.175G>A|p.Gly59Ser |
S264 |
6 | BAA01g17400 | A01 | 8457589 | C | T | missense_variant | MODERATE | c.31G>A|p.Val11Ile |
S167 |
7 | BAA01g17400 | A01 | 8460225 | A | T | upstream_gene_variant | MODIFIER | c.-2520T>A| |
S85 |
8 | BAA01g17400 | A01 | 8461855 | C | T | upstream_gene_variant | MODIFIER | c.-4150G>A| |
S192 |
9 | BAA01g17400 | A01 | 8462366 | C | T | upstream_gene_variant | MODIFIER | c.-4661G>A| |
S136 |