Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00880 | A01 | 391533 | G | A | upstream_gene_variant | MODIFIER | c.-213G>A| |
S168 |
2 | BAA01g00880 | A01 | 392286 | G | A | missense_variant | MODERATE | c.376G>A|p.Val126Ile |
S122 |
3 | BAA01g00880 | A01 | 392709 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.541-1G>A| |
S161 |
4 | BAA01g00880 | A01 | 392934 | C | T | synonymous_variant | LOW | c.675C>T|p.Leu225Leu |
S282 |
5 | BAA01g00880 | A01 | 393211 | C | T | missense_variant | MODERATE | c.800C>T|p.Ser267Leu |
S25 |