Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26630 | A02 | 14901671 | C | T | missense_variant | MODERATE | c.406G>A|p.Glu136Lys |
S250 |
2 | BAA02g26630 | A02 | 14902147 | C | T | missense_variant | MODERATE | c.230G>A|p.Gly77Asp |
S157 S163 |
3 | BAA02g26630 | A02 | 14903975 | G | A | upstream_gene_variant | MODIFIER | c.-1599C>T| |
S236 S262 S263 |
4 | BAA02g26630 | A02 | 14904194 | G | A | upstream_gene_variant | MODIFIER | c.-1818C>T| |
S126 |
5 | BAA02g26630 | A02 | 14905096 | A | G | upstream_gene_variant | MODIFIER | c.-2720T>C| |
S250 |
6 | BAA02g26630 | A02 | 14906603 | G | A | upstream_gene_variant | MODIFIER | c.-4227C>T| |
S57 |
7 | BAA02g26630 | A02 | 14906803 | G | A | upstream_gene_variant | MODIFIER | c.-4427C>T| |
S291 |