Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00150 | A02 | 112945 | G | A | upstream_gene_variant | MODIFIER | c.-2467G>A| |
S33 |
2 | BAA02g00150 | A02 | 113484 | C | T | upstream_gene_variant | MODIFIER | c.-1928C>T| |
S283 |
3 | BAA02g00150 | A02 | 114534 | G | A | upstream_gene_variant | MODIFIER | c.-878G>A| |
S208 S219 |
4 | BAA02g00150 | A02 | 114616 | G | A | upstream_gene_variant | MODIFIER | c.-796G>A| |
S302 |
5 | BAA02g00150 | A02 | 115157 | C | T | upstream_gene_variant | MODIFIER | c.-255C>T| |
S249 |
6 | BAA02g00150 | A02 | 115352 | C | T | upstream_gene_variant | MODIFIER | c.-60C>T| |
S255 |
7 | BAA02g00150 | A02 | 115460 | G | A | missense_variant | MODERATE | c.49G>A|p.Val17Ile |
S12 |
8 | BAA02g00150 | A02 | 116307 | G | A | missense_variant | MODERATE | c.896G>A|p.Gly299Asp |
S237 |
9 | BAA02g00150 | A02 | 116609 | G | A | missense_variant | MODERATE | c.1198G>A|p.Gly400Arg |
S148 S30 S31 |
10 | BAA02g00150 | A02 | 116699 | C | T | synonymous_variant | LOW | c.1288C>T|p.Leu430Leu |
S181 |