Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43450 | A02 | 35986009 | G | A | upstream_gene_variant | MODIFIER | c.-4920G>A| |
S207 |
2 | BAA02g43450 | A02 | 35988744 | G | A | upstream_gene_variant | MODIFIER | c.-2185G>A| |
S148 S31 |
3 | BAA02g43450 | A02 | 35989802 | C | A | upstream_gene_variant | MODIFIER | c.-1127C>A| |
S129 |
4 | BAA02g43450 | A02 | 35991224 | G | A | missense_variant | MODERATE | c.296G>A|p.Gly99Glu |
S297 |
5 | BAA02g43450 | A02 | 35991497 | C | T | missense_variant | MODERATE | c.569C>T|p.Thr190Ile |
S13 |
6 | BAA02g43450 | A02 | 35991577 | G | A | missense_variant | MODERATE | c.649G>A|p.Glu217Lys |
S168 |
7 | BAA02g43450 | A02 | 35992010 | C | T | missense_variant | MODERATE | c.1082C>T|p.Thr361Ile |
S189 |
8 | BAA02g43450 | A02 | 35992723 | C | T | downstream_gene_variant | MODIFIER | c.*613C>T| |
S187 |
9 | BAA02g43450 | A02 | 35993313 | C | T | downstream_gene_variant | MODIFIER | c.*1203C>T| |
S296 |
10 | BAA02g43450 | A02 | 35993475 | C | T | downstream_gene_variant | MODIFIER | c.*1365C>T| |
S283 |
11 | BAA02g43450 | A02 | 35994006 | C | T | downstream_gene_variant | MODIFIER | c.*1896C>T| |
S100 |
12 | BAA02g43450 | A02 | 35994559 | G | A | downstream_gene_variant | MODIFIER | c.*2449G>A| |
S298 |
13 | BAA02g43450 | A02 | 35995992 | G | A | downstream_gene_variant | MODIFIER | c.*3882G>A| |
S81 S85 |