Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g29600 | A08 | 20265316 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1762-1G>A| |
S2 |
2 | BAA08g29600 | A08 | 20265756 | G | A | missense_variant | MODERATE | c.1484C>T|p.Ser495Phe |
S133 |
3 | BAA08g29600 | A08 | 20267166 | C | T | missense_variant | MODERATE | c.535G>A|p.Asp179Asn |
S228 |
4 | BAA08g29600 | A08 | 20270659 | C | T | upstream_gene_variant | MODIFIER | c.-2789G>A| |
S231 |
5 | BAA08g29600 | A08 | 20271540 | G | A | upstream_gene_variant | MODIFIER | c.-3670C>T| |
S100 |