Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g36770 | A03 | 16960693 | G | A | missense_variant | MODERATE | c.493G>A|p.Ala165Thr |
S95 |
2 | BAA03g36770 | A03 | 16961404 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.814-1G>A| |
S39 |
3 | BAA03g36770 | A03 | 16963263 | C | T | missense_variant | MODERATE | c.2047C>T|p.Leu683Phe |
S258 |
4 | BAA03g36770 | A03 | 16965076 | C | T | downstream_gene_variant | MODIFIER | c.*1778C>T| |
S143 |
5 | BAA03g36770 | A03 | 16965558 | C | T | downstream_gene_variant | MODIFIER | c.*2260C>T| |
S81 |