Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10900 | A05 | 5551857 | C | T | missense_variant | MODERATE | c.1048G>A|p.Gly350Arg |
S167 |
2 | BAA05g10900 | A05 | 5553958 | G | A | splice_region_variant&intron_variant | LOW | c.42+8C>T| |
S157 |
3 | BAA05g10900 | A05 | 5556151 | G | A | upstream_gene_variant | MODIFIER | c.-2144C>T| |
S190 |
4 | BAA05g10900 | A05 | 5557029 | C | T | upstream_gene_variant | MODIFIER | c.-3022G>A| |
S276 |
5 | BAA05g10900 | A05 | 5557713 | G | A | upstream_gene_variant | MODIFIER | c.-3706C>T| |
S240 |