Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08930 | A02 | 3948440 | C | T | missense_variant | MODERATE | c.1312G>A|p.Glu438Lys |
S200 |
2 | BAA02g08930 | A02 | 3948525 | G | A | synonymous_variant | LOW | c.1227C>T|p.Leu409Leu |
S235 |
3 | BAA02g08930 | A02 | 3948751 | C | T | missense_variant | MODERATE | c.1069G>A|p.Glu357Lys |
S54 |
4 | BAA02g08930 | A02 | 3949263 | G | A | synonymous_variant | LOW | c.798C>T|p.Phe266Phe |
S229 |
5 | BAA02g08930 | A02 | 3952317 | G | A | synonymous_variant | LOW | c.312C>T|p.Ile104Ile |
S279 |
6 | BAA02g08930 | A02 | 3952899 | C | T | upstream_gene_variant | MODIFIER | c.-271G>A| |
S40 S49 |
7 | BAA02g08930 | A02 | 3953802 | G | A | upstream_gene_variant | MODIFIER | c.-1174C>T| |
S114 |
8 | BAA02g08930 | A02 | 3953922 | C | T | upstream_gene_variant | MODIFIER | c.-1294G>A| |
S290 |
9 | BAA02g08930 | A02 | 3954649 | G | A | upstream_gene_variant | MODIFIER | c.-2021C>T| |
S12 |
10 | BAA02g08930 | A02 | 3955111 | C | T | upstream_gene_variant | MODIFIER | c.-2483G>A| |
S112 |
11 | BAA02g08930 | A02 | 3956541 | G | A | upstream_gene_variant | MODIFIER | c.-3913C>T| |
S5 |