Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g48620 | A09 | 52367178 | G | A | missense_variant | MODERATE | c.2077C>T|p.Leu693Phe |
S291 |
2 | BAA09g48620 | A09 | 52370441 | G | A | splice_region_variant&synonymous_variant | LOW | c.681C>T|p.Ile227Ile |
S16 |
3 | BAA09g48620 | A09 | 52370641 | C | T | missense_variant | MODERATE | c.481G>A|p.Glu161Lys |
S87 |
4 | BAA09g48620 | A09 | 52375049 | C | T | upstream_gene_variant | MODIFIER | c.-3928G>A| |
S138 |
5 | BAA09g48620 | A09 | 52376059 | A | G | upstream_gene_variant | MODIFIER | c.-4938T>C| |
S8 |