Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45460 | A01 | 30311679 | C | T | missense_variant | MODERATE | c.775G>A|p.Gly259Arg |
S232 |
2 | BAA01g45460 | A01 | 30311714 | C | T | missense_variant | MODERATE | c.740G>A|p.Arg247Lys |
S132 S215 S89 |
3 | BAA01g45460 | A01 | 30311928 | C | T | missense_variant | MODERATE | c.526G>A|p.Glu176Lys |
S182 |
4 | BAA01g45460 | A01 | 30312222 | C | T | missense_variant | MODERATE | c.232G>A|p.Glu78Lys |
S292 |
5 | BAA01g45460 | A01 | 30312565 | G | A | upstream_gene_variant | MODIFIER | c.-112C>T| |
S187 |
6 | BAA01g45460 | A01 | 30314446 | C | T | upstream_gene_variant | MODIFIER | c.-1993G>A| |
S16 |
7 | BAA01g45460 | A01 | 30314826 | C | T | upstream_gene_variant | MODIFIER | c.-2373G>A| |
S201 |
8 | BAA01g45460 | A01 | 30315115 | C | T | upstream_gene_variant | MODIFIER | c.-2662G>A| |
S183 S198 |
9 | BAA01g45460 | A01 | 30315768 | G | A | upstream_gene_variant | MODIFIER | c.-3315C>T| |
S33 |
10 | BAA01g45460 | A01 | 30315816 | C | T | upstream_gene_variant | MODIFIER | c.-3363G>A| |
S264 |