Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10740 | A02 | 4806326 | G | A | downstream_gene_variant | MODIFIER | c.*901C>T| |
S139 |
2 | BAA02g10740 | A02 | 4806972 | G | A | downstream_gene_variant | MODIFIER | c.*255C>T| |
S172 S202 S217 |
3 | BAA02g10740 | A02 | 4807571 | G | A | intron_variant | MODIFIER | c.979+88C>T| |
S133 |
4 | BAA02g10740 | A02 | 4807966 | G | A | missense_variant | MODERATE | c.833C>T|p.Thr278Ile |
S107 |
5 | BAA02g10740 | A02 | 4808613 | C | T | intron_variant | MODIFIER | c.600+210G>A| |
S67 |
6 | BAA02g10740 | A02 | 4808965 | C | T | intron_variant | MODIFIER | c.486-28G>A| |
S283 |
7 | BAA02g10740 | A02 | 4810259 | G | A | missense_variant | MODERATE | c.7C>T|p.Leu3Phe |
S164 |
8 | BAA02g10740 | A02 | 4812276 | G | A | upstream_gene_variant | MODIFIER | c.-2011C>T| |
S27 |