Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14270 | A02 | 6677098 | G | A | missense_variant | MODERATE | c.386C>T|p.Pro129Leu |
S82 S92 |
2 | BAA02g14270 | A02 | 6677961 | C | T | upstream_gene_variant | MODIFIER | c.-243G>A| |
S92 |
3 | BAA02g14270 | A02 | 6679105 | G | A | upstream_gene_variant | MODIFIER | c.-1387C>T| |
S282 |
4 | BAA02g14270 | A02 | 6680141 | G | A | upstream_gene_variant | MODIFIER | c.-2423C>T| |
S256 |
5 | BAA02g14270 | A02 | 6680217 | C | G | upstream_gene_variant | MODIFIER | c.-2499G>C| |
S108 |
6 | BAA02g14270 | A02 | 6680416 | T | A | upstream_gene_variant | MODIFIER | c.-2698A>T| |
S257 |