Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42200 | A02 | 35181260 | G | A | missense_variant | MODERATE | c.1586C>T|p.Ser529Leu |
S159 S243 |
2 | BAA02g42200 | A02 | 35182539 | C | T | missense_variant&splice_region_variant | MODERATE | c.824G>A|p.Gly275Asp |
S186 |
3 | BAA02g42200 | A02 | 35183772 | C | T | missense_variant | MODERATE | c.121G>A|p.Ala41Thr |
S114 |
4 | BAA02g42200 | A02 | 35183930 | G | A | synonymous_variant | LOW | c.40C>T|p.Leu14Leu |
S51 |
5 | BAA02g42200 | A02 | 35184493 | C | T | upstream_gene_variant | MODIFIER | c.-524G>A| |
S72 |
6 | BAA02g42200 | A02 | 35184859 | G | A | upstream_gene_variant | MODIFIER | c.-890C>T| |
S177 |
7 | BAA02g42200 | A02 | 35184938 | G | A | upstream_gene_variant | MODIFIER | c.-969C>T| |
S69 |
8 | BAA02g42200 | A02 | 35185797 | C | T | upstream_gene_variant | MODIFIER | c.-1828G>A| |
S6 |
9 | BAA02g42200 | A02 | 35186309 | G | A | upstream_gene_variant | MODIFIER | c.-2340C>T| |
S136 |
10 | BAA02g42200 | A02 | 35186583 | C | T | upstream_gene_variant | MODIFIER | c.-2614G>A| |
S75 S81 |
11 | BAA02g42200 | A02 | 35186637 | C | T | upstream_gene_variant | MODIFIER | c.-2668G>A| |
S118 |
12 | BAA02g42200 | A02 | 35188400 | G | A | upstream_gene_variant | MODIFIER | c.-4431C>T| |
S36 |