Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21690 | A02 | 11665070 | G | A | missense_variant | MODERATE | c.637C>T|p.Pro213Ser |
S148 S210 |
2 | BAA02g21690 | A02 | 11665430 | C | T | missense_variant | MODERATE | c.377G>A|p.Gly126Glu |
S144 |
3 | BAA02g21690 | A02 | 11668568 | C | T | upstream_gene_variant | MODIFIER | c.-521G>A| |
S104 S52 |
4 | BAA02g21690 | A02 | 11668926 | C | T | upstream_gene_variant | MODIFIER | c.-879G>A| |
S42 |
5 | BAA02g21690 | A02 | 11668970 | G | A | upstream_gene_variant | MODIFIER | c.-923C>T| |
S110 |
6 | BAA02g21690 | A02 | 11669451 | C | T | upstream_gene_variant | MODIFIER | c.-1404G>A| |
S185 |
7 | BAA02g21690 | A02 | 11670291 | G | A | upstream_gene_variant | MODIFIER | c.-2244C>T| |
S122 |
8 | BAA02g21690 | A02 | 11672692 | G | A | upstream_gene_variant | MODIFIER | c.-4645C>T| |
S263 |