Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09860 | A02 | 4343955 | G | A | missense_variant | MODERATE | c.217G>A|p.Asp73Asn |
S159 S243 |
2 | BAA02g09860 | A02 | 4344098 | C | T | missense_variant | MODERATE | c.278C>T|p.Thr93Ile |
S219 S72 |
3 | BAA02g09860 | A02 | 4345234 | G | A | missense_variant | MODERATE | c.706G>A|p.Glu236Lys |
S144 |
4 | BAA02g09860 | A02 | 4346674 | G | A | missense_variant | MODERATE | c.1033G>A|p.Glu345Lys |
S140 |
5 | BAA02g09860 | A02 | 4347287 | G | A | missense_variant | MODERATE | c.1465G>A|p.Glu489Lys |
S149 |
6 | BAA02g09860 | A02 | 4349299 | C | T | downstream_gene_variant | MODIFIER | c.*1075C>T| |
S305 |
7 | BAA02g09860 | A02 | 4349388 | C | T | downstream_gene_variant | MODIFIER | c.*1164C>T| |
S15 S3 |
8 | BAA02g09860 | A02 | 4351489 | G | A | downstream_gene_variant | MODIFIER | c.*3265G>A| |
S48 |
9 | BAA02g09860 | A02 | 4351542 | G | A | downstream_gene_variant | MODIFIER | c.*3318G>A| |
S197 |
10 | BAA02g09860 | A02 | 4351577 | G | A | downstream_gene_variant | MODIFIER | c.*3353G>A| |
S296 |
11 | BAA02g09860 | A02 | 4351622 | C | T | downstream_gene_variant | MODIFIER | c.*3398C>T| |
S9 |
12 | BAA02g09860 | A02 | 4351715 | G | A | downstream_gene_variant | MODIFIER | c.*3491G>A| |
S165 |