Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g04900 | A09 | 2846687 | C | T | intron_variant | MODIFIER | c.538+781G>A| |
S77 S82 |
2 | BAA09g04900 | A09 | 2847813 | G | A | missense_variant | MODERATE | c.193C>T|p.Leu65Phe |
S73 S91 |
3 | BAA09g04900 | A09 | 2847919 | C | T | synonymous_variant | LOW | c.87G>A|p.Gln29Gln |
S18 |
4 | BAA09g04900 | A09 | 2848814 | C | T | upstream_gene_variant | MODIFIER | c.-809G>A| |
S171 |
5 | BAA09g04900 | A09 | 2849471 | C | T | upstream_gene_variant | MODIFIER | c.-1466G>A| |
S118 S54 |