Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09120 | A05 | 4558141 | C | T | upstream_gene_variant | MODIFIER | c.-213C>T| |
S197 |
2 | BAA05g09120 | A05 | 4559174 | C | T | missense_variant | MODERATE | c.572C>T|p.Thr191Ile |
S191 |
3 | BAA05g09120 | A05 | 4559389 | G | A | synonymous_variant | LOW | c.717G>A|p.Gly239Gly |
S158 |
4 | BAA05g09120 | A05 | 4559493 | G | A | missense_variant | MODERATE | c.821G>A|p.Gly274Glu |
S257 |
5 | BAA05g09120 | A05 | 4559662 | C | T | synonymous_variant | LOW | c.912C>T|p.Leu304Leu |
S2 |
6 | BAA05g09120 | A05 | 4560352 | C | T | missense_variant&splice_region_variant | MODERATE | c.1291C>T|p.Leu431Phe |
S116 |
7 | BAA05g09120 | A05 | 4560598 | G | A | synonymous_variant | LOW | c.1455G>A|p.Leu485Leu |
S173 |
8 | BAA05g09120 | A05 | 4560629 | C | T | missense_variant | MODERATE | c.1486C>T|p.Leu496Phe |
S182 |