Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16170 | A02 | 7876899 | C | T | missense_variant | MODERATE | c.928G>A|p.Asp310Asn |
S135 |
2 | BAA02g16170 | A02 | 7877142 | G | A | missense_variant | MODERATE | c.685C>T|p.Arg229Cys |
S136 |
3 | BAA02g16170 | A02 | 7877681 | C | T | missense_variant | MODERATE | c.341G>A|p.Arg114Lys |
S13 |
4 | BAA02g16170 | A02 | 7881030 | C | T | upstream_gene_variant | MODIFIER | c.-3009G>A| |
S255 |
5 | BAA02g16170 | A02 | 7882138 | C | T | upstream_gene_variant | MODIFIER | c.-4117G>A| |
S181 |
6 | BAA02g16170 | A02 | 7882275 | G | A | upstream_gene_variant | MODIFIER | c.-4254C>T| |
S159 S243 |
7 | BAA02g16170 | A02 | 7882318 | G | A | upstream_gene_variant | MODIFIER | c.-4297C>T| |
S260 |
8 | BAA02g16170 | A02 | 7882989 | C | T | upstream_gene_variant | MODIFIER | c.-4968G>A| |
S138 |