Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g17980 | A01 | 8797071 | C | T | upstream_gene_variant | MODIFIER | c.-4932C>T| |
S170 |
2 | BAA01g17980 | A01 | 8802270 | G | A | missense_variant | MODERATE | c.268G>A|p.Gly90Arg |
S37 |
3 | BAA01g17980 | A01 | 8802779 | C | T | synonymous_variant | LOW | c.777C>T|p.Phe259Phe |
S295 |
4 | BAA01g17980 | A01 | 8803004 | G | A | synonymous_variant | LOW | c.1002G>A|p.Pro334Pro |
S213 |
5 | BAA01g17980 | A01 | 8803686 | C | T | missense_variant | MODERATE | c.1684C>T|p.Leu562Phe |
S19 |
6 | BAA01g17980 | A01 | 8803752 | G | A | missense_variant | MODERATE | c.1750G>A|p.Glu584Lys |
S298 |
7 | BAA01g17980 | A01 | 8804278 | G | A | missense_variant | MODERATE | c.2276G>A|p.Arg759Lys |
S197 |
8 | BAA01g17980 | A01 | 8804835 | C | T | downstream_gene_variant | MODIFIER | c.*109C>T| |
S51 |
9 | BAA01g17980 | A01 | 8804871 | G | A | downstream_gene_variant | MODIFIER | c.*145G>A| |
S294 |