Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g63680 | A09 | 59472447 | C | T | missense_variant | MODERATE | c.689C>T|p.Pro230Leu |
S99 |
2 | BAA09g63680 | A09 | 59472621 | C | T | missense_variant | MODERATE | c.863C>T|p.Ser288Phe |
S217 S248 |
3 | BAA09g63680 | A09 | 59473384 | C | T | synonymous_variant | LOW | c.1149C>T|p.Asn383Asn |
S172 S217 |
4 | BAA09g63680 | A09 | 59473389 | C | T | missense_variant | MODERATE | c.1154C>T|p.Ala385Val |
S270 |
5 | BAA09g63680 | A09 | 59474907 | C | T | downstream_gene_variant | MODIFIER | c.*935C>T| |
S225 |