Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00050 | A02 | 39107 | G | A | missense_variant | MODERATE | c.404C>T|p.Ser135Phe |
S50 |
2 | BAA02g00050 | A02 | 39240 | C | T | missense_variant | MODERATE | c.271G>A|p.Val91Met |
S61 |
3 | BAA02g00050 | A02 | 39282 | C | T | missense_variant | MODERATE | c.229G>A|p.Glu77Lys |
S194 |
4 | BAA02g00050 | A02 | 40719 | G | A | upstream_gene_variant | MODIFIER | c.-1209C>T| |
S163 |
5 | BAA02g00050 | A02 | 41963 | C | T | upstream_gene_variant | MODIFIER | c.-2453G>A| |
S199 |
6 | BAA02g00050 | A02 | 43263 | C | T | upstream_gene_variant | MODIFIER | c.-3753G>A| |
S252 |
7 | BAA02g00050 | A02 | 43457 | G | A | upstream_gene_variant | MODIFIER | c.-3947C>T| |
S221 |