Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29350 | A02 | 16797397 | C | T | synonymous_variant | LOW | c.76C>T|p.Leu26Leu |
S296 |
2 | BAA02g29350 | A02 | 16797563 | C | T | missense_variant | MODERATE | c.242C>T|p.Ser81Phe |
S171 |
3 | BAA02g29350 | A02 | 16798361 | G | A | intron_variant | MODIFIER | c.1008+32G>A| |
S98 |
4 | BAA02g29350 | A02 | 16798671 | C | T | intron_variant | MODIFIER | c.1009-44C>T| |
S179 |
5 | BAA02g29350 | A02 | 16798802 | G | A | missense_variant | MODERATE | c.1096G>A|p.Gly366Ser |
S265 |
6 | BAA02g29350 | A02 | 16799583 | C | T | downstream_gene_variant | MODIFIER | c.*491C>T| |
S32 |
7 | BAA02g29350 | A02 | 16800161 | C | T | downstream_gene_variant | MODIFIER | c.*1069C>T| |
S18 |
8 | BAA02g29350 | A02 | 16800198 | G | A | downstream_gene_variant | MODIFIER | c.*1106G>A| |
S197 |
9 | BAA02g29350 | A02 | 16800838 | C | T | downstream_gene_variant | MODIFIER | c.*1746C>T| |
S308 |
10 | BAA02g29350 | A02 | 16800881 | C | T | downstream_gene_variant | MODIFIER | c.*1789C>T| |
S296 |
11 | BAA02g29350 | A02 | 16800899 | G | A | downstream_gene_variant | MODIFIER | c.*1807G>A| |
S116 |