Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05140 | A02 | 2262629 | G | A | upstream_gene_variant | MODIFIER | c.-668G>A| |
S163 |
2 | BAA02g05140 | A02 | 2263842 | C | T | intron_variant | MODIFIER | c.291-226C>T| |
S38 |
3 | BAA02g05140 | A02 | 2264031 | G | A | intron_variant | MODIFIER | c.291-37G>A| |
S146 |
4 | BAA02g05140 | A02 | 2264234 | C | T | intron_variant | MODIFIER | c.393-21C>T| |
S42 |
5 | BAA02g05140 | A02 | 2266016 | C | T | missense_variant | MODERATE | c.1595C>T|p.Ser532Phe |
S200 |