Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10930 | A02 | 4897298 | G | A | downstream_gene_variant | MODIFIER | c.*1251C>T| |
S235 |
2 | BAA02g10930 | A02 | 4898709 | C | T | missense_variant&splice_region_variant | MODERATE | c.2381G>A|p.Gly794Glu |
S18 |
3 | BAA02g10930 | A02 | 4899674 | G | A | missense_variant | MODERATE | c.1702C>T|p.Pro568Ser |
S169 |
4 | BAA02g10930 | A02 | 4899701 | C | T | missense_variant | MODERATE | c.1675G>A|p.Gly559Arg |
S130 |
5 | BAA02g10930 | A02 | 4899732 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1645-1G>A| |
S47 |
6 | BAA02g10930 | A02 | 4900692 | C | T | missense_variant | MODERATE | c.1141G>A|p.Val381Met |
S208 |
7 | BAA02g10930 | A02 | 4900733 | C | T | missense_variant | MODERATE | c.1100G>A|p.Arg367Lys |
S263 |
8 | BAA02g10930 | A02 | 4902052 | G | A | synonymous_variant | LOW | c.408C>T|p.Asn136Asn |
S187 |
9 | BAA02g10930 | A02 | 4902819 | G | A | upstream_gene_variant | MODIFIER | c.-195C>T| |
S197 |
10 | BAA02g10930 | A02 | 4904607 | C | T | upstream_gene_variant | MODIFIER | c.-1983G>A| |
S71 |
11 | BAA02g10930 | A02 | 4905621 | C | T | upstream_gene_variant | MODIFIER | c.-2997G>A| |
S206 |
12 | BAA02g10930 | A02 | 4905651 | G | A | upstream_gene_variant | MODIFIER | c.-3027C>T| |
S61 |
13 | BAA02g10930 | A02 | 4906834 | C | T | upstream_gene_variant | MODIFIER | c.-4210G>A| |
S257 |
14 | BAA02g10930 | A02 | 4907621 | C | T | upstream_gene_variant | MODIFIER | c.-4997G>A| |
S40 S49 |