Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01330 | A02 | 610810 | C | T | synonymous_variant | LOW | c.2016G>A|p.Arg672Arg |
S150 |
2 | BAA02g01330 | A02 | 612421 | C | T | missense_variant | MODERATE | c.1264G>A|p.Gly422Arg |
S2 |
3 | BAA02g01330 | A02 | 612881 | C | T | missense_variant | MODERATE | c.1046G>A|p.Gly349Glu |
S34 |
4 | BAA02g01330 | A02 | 613651 | C | T | missense_variant | MODERATE | c.800G>A|p.Arg267Lys |
S174 S216 S39 |
5 | BAA02g01330 | A02 | 614047 | C | T | missense_variant | MODERATE | c.586G>A|p.Val196Ile |
S219 |
6 | BAA02g01330 | A02 | 615397 | C | T | upstream_gene_variant | MODIFIER | c.-34G>A| |
S1 S90 |
7 | BAA02g01330 | A02 | 615822 | G | A | upstream_gene_variant | MODIFIER | c.-459C>T| |
S165 |
8 | BAA02g01330 | A02 | 615892 | C | T | upstream_gene_variant | MODIFIER | c.-529G>A| |
S278 |
9 | BAA02g01330 | A02 | 616064 | G | A | upstream_gene_variant | MODIFIER | c.-701C>T| |
S261 |
10 | BAA02g01330 | A02 | 616087 | G | A | upstream_gene_variant | MODIFIER | c.-724C>T| |
S76 |
11 | BAA02g01330 | A02 | 616411 | G | A | upstream_gene_variant | MODIFIER | c.-1048C>T| |
S143 |
12 | BAA02g01330 | A02 | 619066 | A | T | upstream_gene_variant | MODIFIER | c.-3703T>A| |
S183 S198 |
13 | BAA02g01330 | A02 | 619194 | C | T | upstream_gene_variant | MODIFIER | c.-3831G>A| |
S130 |