Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49090 | A09 | 52624946 | C | T | missense_variant | MODERATE | c.253G>A|p.Asp85Asn |
S63 |
2 | BAA09g49090 | A09 | 52624996 | G | A | missense_variant | MODERATE | c.203C>T|p.Ser68Phe |
S161 |
3 | BAA09g49090 | A09 | 52625023 | G | A | missense_variant | MODERATE | c.176C>T|p.Ala59Val |
S178 |
4 | BAA09g49090 | A09 | 52626193 | G | A | upstream_gene_variant | MODIFIER | c.-995C>T| |
S184 |
5 | BAA09g49090 | A09 | 52628104 | C | T | upstream_gene_variant | MODIFIER | c.-2906G>A| |
S212 |
6 | BAA09g49090 | A09 | 52628120 | G | A | upstream_gene_variant | MODIFIER | c.-2922C>T| |
S234 |