Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20960 | A02 | 11175261 | C | T | missense_variant | MODERATE | c.778G>A|p.Ala260Thr |
S185 |
2 | BAA02g20960 | A02 | 11176089 | C | T | missense_variant | MODERATE | c.415G>A|p.Asp139Asn |
S183 S198 |
3 | BAA02g20960 | A02 | 11176140 | C | T | missense_variant | MODERATE | c.364G>A|p.Glu122Lys |
S38 |
4 | BAA02g20960 | A02 | 11177067 | G | A | synonymous_variant | LOW | c.6C>T|p.Ile2Ile |
S34 |
5 | BAA02g20960 | A02 | 11179219 | G | A | upstream_gene_variant | MODIFIER | c.-2147C>T| |
S64 |
6 | BAA02g20960 | A02 | 11180017 | G | A | upstream_gene_variant | MODIFIER | c.-2945C>T| |
S232 |
7 | BAA02g20960 | A02 | 11180416 | G | A | upstream_gene_variant | MODIFIER | c.-3344C>T| |
S274 |