Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38280 | A02 | 32621587 | G | A | missense_variant | MODERATE | c.1028C>T|p.Thr343Ile |
S229 |
2 | BAA02g38280 | A02 | 32623091 | C | T | upstream_gene_variant | MODIFIER | c.-477G>A| |
S92 |
3 | BAA02g38280 | A02 | 32623493 | G | A | upstream_gene_variant | MODIFIER | c.-879C>T| |
S25 |
4 | BAA02g38280 | A02 | 32624147 | C | T | upstream_gene_variant | MODIFIER | c.-1533G>A| |
S167 |
5 | BAA02g38280 | A02 | 32625300 | C | T | upstream_gene_variant | MODIFIER | c.-2686G>A| |
S23 |
6 | BAA02g38280 | A02 | 32626912 | C | T | upstream_gene_variant | MODIFIER | c.-4298G>A| |
S39 |