Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g27660 | A09 | 18117097 | C | T | missense_variant | MODERATE | c.1273G>A|p.Glu425Lys |
S144 |
2 | BAA09g27660 | A09 | 18117302 | C | T | synonymous_variant | LOW | c.1068G>A|p.Lys356Lys |
S139 |
3 | BAA09g27660 | A09 | 18118094 | G | A | synonymous_variant | LOW | c.276C>T|p.Pro92Pro |
S207 |
4 | BAA09g27660 | A09 | 18121096 | G | A | upstream_gene_variant | MODIFIER | c.-2727C>T| |
S1 S90 |
5 | BAA09g27660 | A09 | 18122790 | C | T | upstream_gene_variant | MODIFIER | c.-4421G>A| |
S182 |
6 | BAA09g27660 | A09 | 18122998 | C | T | upstream_gene_variant | MODIFIER | c.-4629G>A| |
S5 |