Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22000 | A09 | 13748554 | G | A | synonymous_variant | LOW | c.2745C>T|p.Asn915Asn |
S87 |
2 | BAA09g22000 | A09 | 13749053 | C | T | missense_variant | MODERATE | c.2347G>A|p.Gly783Arg |
S278 |
3 | BAA09g22000 | A09 | 13749369 | G | A | splice_region_variant&synonymous_variant | LOW | c.2278C>T|p.Leu760Leu |
S183 S198 |
4 | BAA09g22000 | A09 | 13751009 | C | T | synonymous_variant | LOW | c.987G>A|p.Leu329Leu |
S135 |
5 | BAA09g22000 | A09 | 13758068 | C | T | upstream_gene_variant | MODIFIER | c.-4882G>A| |
S294 |