Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g07690 | A05 | 3815219 | G | A | downstream_gene_variant | MODIFIER | c.*1420C>T| |
S34 |
2 | BAA05g07690 | A05 | 3817420 | C | T | missense_variant | MODERATE | c.715G>A|p.Ala239Thr |
S19 |
3 | BAA05g07690 | A05 | 3818548 | G | A | synonymous_variant | LOW | c.171C>T|p.Asn57Asn |
S40 S49 |
4 | BAA05g07690 | A05 | 3821043 | C | T | upstream_gene_variant | MODIFIER | c.-2225G>A| |
S243 |
5 | BAA05g07690 | A05 | 3821174 | C | T | upstream_gene_variant | MODIFIER | c.-2356G>A| |
S235 |
6 | BAA05g07690 | A05 | 3821221 | C | T | upstream_gene_variant | MODIFIER | c.-2403G>A| |
S81 |
7 | BAA05g07690 | A05 | 3821308 | G | A | upstream_gene_variant | MODIFIER | c.-2490C>T| |
S48 |
8 | BAA05g07690 | A05 | 3821931 | C | T | upstream_gene_variant | MODIFIER | c.-3113G>A| |
S98 |
9 | BAA05g07690 | A05 | 3822432 | C | T | upstream_gene_variant | MODIFIER | c.-3614G>A| |
S199 |
10 | BAA05g07690 | A05 | 3823331 | G | A | upstream_gene_variant | MODIFIER | c.-4513C>T| |
S80 |