Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49940 | A09 | 53039731 | G | A | upstream_gene_variant | MODIFIER | c.-344G>A| |
S116 |
2 | BAA09g49940 | A09 | 53040411 | C | T | missense_variant | MODERATE | c.337C>T|p.Pro113Ser |
S182 |
3 | BAA09g49940 | A09 | 53041834 | C | T | splice_region_variant&intron_variant | LOW | c.986+5C>T| |
S186 |
4 | BAA09g49940 | A09 | 53042440 | C | T | synonymous_variant | LOW | c.1227C>T|p.Phe409Phe |
S152 |