Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46470 | A02 | 37766979 | C | T | missense_variant | MODERATE | c.631G>A|p.Asp211Asn |
S107 |
2 | BAA02g46470 | A02 | 37767079 | C | T | synonymous_variant | LOW | c.531G>A|p.Lys177Lys |
S189 |
3 | BAA02g46470 | A02 | 37768240 | A | C | missense_variant | MODERATE | c.83T>G|p.Leu28Arg |
S158 S55 S75 |
4 | BAA02g46470 | A02 | 37768242 | G | A | synonymous_variant | LOW | c.81C>T|p.Asp27Asp |
S113 |
5 | BAA02g46470 | A02 | 37770642 | G | A | upstream_gene_variant | MODIFIER | c.-2320C>T| |
S235 |
6 | BAA02g46470 | A02 | 37772694 | C | T | upstream_gene_variant | MODIFIER | c.-4372G>A| |
S9 |
7 | BAA02g46470 | A02 | 37773168 | C | T | upstream_gene_variant | MODIFIER | c.-4846G>A| |
S159 S187 S188 S243 S276 S299 |
8 | BAA02g46470 | A02 | 37773221 | C | T | upstream_gene_variant | MODIFIER | c.-4899G>A| |
S157 |