Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g48230 | A02 | 38733345 | C | T | missense_variant | MODERATE | c.527G>A|p.Arg176Lys |
S269 |
2 | BAA02g48230 | A02 | 38733373 | G | A | missense_variant | MODERATE | c.499C>T|p.Leu167Phe |
S130 |
3 | BAA02g48230 | A02 | 38734221 | C | T | missense_variant | MODERATE | c.5G>A|p.Gly2Asp |
S69 |
4 | BAA02g48230 | A02 | 38735400 | G | A | upstream_gene_variant | MODIFIER | c.-1175C>T| |
S37 |
5 | BAA02g48230 | A02 | 38735894 | C | T | upstream_gene_variant | MODIFIER | c.-1669G>A| |
S241 |
6 | BAA02g48230 | A02 | 38737143 | C | T | upstream_gene_variant | MODIFIER | c.-2918G>A| |
S244 |
7 | BAA02g48230 | A02 | 38737458 | C | T | upstream_gene_variant | MODIFIER | c.-3233G>A| |
S65 |
8 | BAA02g48230 | A02 | 38737944 | C | T | upstream_gene_variant | MODIFIER | c.-3719G>A| |
S193 |
9 | BAA02g48230 | A02 | 38737999 | G | A | upstream_gene_variant | MODIFIER | c.-3774C>T| |
S278 |