Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g68940 | A09 | 61771265 | C | T | missense_variant | MODERATE | c.1231G>A|p.Asp411Asn |
S120 |
2 | BAA09g68940 | A09 | 61773347 | G | A | synonymous_variant | LOW | c.141C>T|p.Phe47Phe |
S16 |
3 | BAA09g68940 | A09 | 61775283 | G | A | upstream_gene_variant | MODIFIER | c.-1796C>T| |
S202 |
4 | BAA09g68940 | A09 | 61777232 | G | A | upstream_gene_variant | MODIFIER | c.-3745C>T| |
S234 |
5 | BAA09g68940 | A09 | 61778002 | C | T | upstream_gene_variant | MODIFIER | c.-4515G>A| |
S175 |