Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g04120 | A01 | 1856174 | G | A | missense_variant | MODERATE | c.2213C>T|p.Pro738Leu |
S156 |
2 | BAA01g04120 | A01 | 1856323 | G | A | synonymous_variant | LOW | c.2064C>T|p.Leu688Leu |
S177 |
3 | BAA01g04120 | A01 | 1859756 | C | T | upstream_gene_variant | MODIFIER | c.-825G>A| |
S168 |
4 | BAA01g04120 | A01 | 1860611 | C | T | upstream_gene_variant | MODIFIER | c.-1680G>A| |
S100 |
5 | BAA01g04120 | A01 | 1860624 | T | C | upstream_gene_variant | MODIFIER | c.-1693A>G| |
S291 |
6 | BAA01g04120 | A01 | 1861366 | C | T | upstream_gene_variant | MODIFIER | c.-2435G>A| |
S130 |
7 | BAA01g04120 | A01 | 1861529 | G | A | upstream_gene_variant | MODIFIER | c.-2598C>T| |
S251 |