Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02820 | A02 | 1274303 | C | T | missense_variant | MODERATE | c.578G>A|p.Gly193Asp |
S281 |
2 | BAA02g02820 | A02 | 1274330 | G | A | missense_variant | MODERATE | c.551C>T|p.Ala184Val |
S149 S93 |
3 | BAA02g02820 | A02 | 1275746 | G | A | missense_variant | MODERATE | c.88C>T|p.Leu30Phe |
S209 |
4 | BAA02g02820 | A02 | 1277843 | C | T | upstream_gene_variant | MODIFIER | c.-2010G>A| |
S82 S92 |
5 | BAA02g02820 | A02 | 1278227 | G | A | upstream_gene_variant | MODIFIER | c.-2394C>T| |
S282 |
6 | BAA02g02820 | A02 | 1278267 | C | T | upstream_gene_variant | MODIFIER | c.-2434G>A| |
S211 S227 |
7 | BAA02g02820 | A02 | 1278451 | C | T | upstream_gene_variant | MODIFIER | c.-2618G>A| |
S207 |
8 | BAA02g02820 | A02 | 1278751 | C | T | upstream_gene_variant | MODIFIER | c.-2918G>A| |
S229 |
9 | BAA02g02820 | A02 | 1278886 | C | T | upstream_gene_variant | MODIFIER | c.-3053G>A| |
S116 |