Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22090 | A01 | 11010358 | G | A | synonymous_variant | LOW | c.492C>T|p.Thr164Thr |
S298 |
2 | BAA01g22090 | A01 | 11010457 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.394-1G>A| |
S205 |
3 | BAA01g22090 | A01 | 11010593 | G | A | missense_variant | MODERATE | c.332C>T|p.Ala111Val |
S244 |
4 | BAA01g22090 | A01 | 11011570 | C | T | missense_variant | MODERATE | c.14G>A|p.Gly5Glu |
S38 |
5 | BAA01g22090 | A01 | 11013919 | G | A | upstream_gene_variant | MODIFIER | c.-2336C>T| |
S95 |
6 | BAA01g22090 | A01 | 11015297 | G | A | upstream_gene_variant | MODIFIER | c.-3714C>T| |
S209 |