Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18380 | A01 | 9017656 | G | A | missense_variant | MODERATE | c.221G>A|p.Gly74Asp |
S110 |
2 | BAA01g18380 | A01 | 9019002 | G | A | synonymous_variant | LOW | c.1455G>A|p.Pro485Pro |
S116 |
3 | BAA01g18380 | A01 | 9021516 | C | T | downstream_gene_variant | MODIFIER | c.*2481C>T| |
S77 |
4 | BAA01g18380 | A01 | 9022912 | C | T | downstream_gene_variant | MODIFIER | c.*3877C>T| |
S58 |
5 | BAA01g18380 | A01 | 9023102 | G | A | downstream_gene_variant | MODIFIER | c.*4067G>A| |
S180 |
6 | BAA01g18380 | A01 | 9023319 | C | T | downstream_gene_variant | MODIFIER | c.*4284C>T| |
S294 |
7 | BAA01g18380 | A01 | 9023380 | G | A | downstream_gene_variant | MODIFIER | c.*4345G>A| |
S209 |
8 | BAA01g18380 | A01 | 9023496 | G | A | downstream_gene_variant | MODIFIER | c.*4461G>A| |
S28 |