Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g14000 | A05 | 7325972 | C | T | missense_variant | MODERATE | c.401C>T|p.Ala134Val |
S289 S290 |
2 | BAA05g14000 | A05 | 7326110 | C | T | missense_variant | MODERATE | c.539C>T|p.Pro180Leu |
S105 S106 |
3 | BAA05g14000 | A05 | 7326639 | C | T | downstream_gene_variant | MODIFIER | c.*420C>T| |
S69 |
4 | BAA05g14000 | A05 | 7327318 | G | A | downstream_gene_variant | MODIFIER | c.*1099G>A| |
S13 |
5 | BAA05g14000 | A05 | 7327564 | A | T | downstream_gene_variant | MODIFIER | c.*1345A>T| |
S158 |
6 | BAA05g14000 | A05 | 7327762 | G | C | downstream_gene_variant | MODIFIER | c.*1543G>C| |
S144 S230 S232 S233 S306 |
7 | BAA05g14000 | A05 | 7328432 | C | T | downstream_gene_variant | MODIFIER | c.*2213C>T| |
S85 |
8 | BAA05g14000 | A05 | 7330145 | C | T | downstream_gene_variant | MODIFIER | c.*3926C>T| |
S251 |
9 | BAA05g14000 | A05 | 7330822 | G | A | downstream_gene_variant | MODIFIER | c.*4603G>A| |
S299 |