Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00280 | A02 | 160625 | G | A | upstream_gene_variant | MODIFIER | c.-4480G>A| |
S25 |
2 | BAA02g00280 | A02 | 162502 | C | T | upstream_gene_variant | MODIFIER | c.-2603C>T| |
S6 |
3 | BAA02g00280 | A02 | 163027 | G | A | upstream_gene_variant | MODIFIER | c.-2078G>A| |
S51 |
4 | BAA02g00280 | A02 | 164337 | C | T | upstream_gene_variant | MODIFIER | c.-768C>T| |
S167 |
5 | BAA02g00280 | A02 | 165156 | G | A | missense_variant | MODERATE | c.52G>A|p.Val18Ile |
S265 |
6 | BAA02g00280 | A02 | 165430 | G | A | missense_variant | MODERATE | c.326G>A|p.Gly109Asp |
S60 |
7 | BAA02g00280 | A02 | 165498 | G | A | missense_variant | MODERATE | c.394G>A|p.Glu132Lys |
S25 |
8 | BAA02g00280 | A02 | 165757 | G | A | missense_variant | MODERATE | c.571G>A|p.Asp191Asn |
S53 |
9 | BAA02g00280 | A02 | 166142 | G | A | synonymous_variant | LOW | c.873G>A|p.Lys291Lys |
S10 |
10 | BAA02g00280 | A02 | 166609 | G | A | missense_variant | MODERATE | c.1340G>A|p.Gly447Glu |
S156 |