Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10070 | A02 | 4441665 | C | T | upstream_gene_variant | MODIFIER | c.-4020C>T| |
S117 |
2 | BAA02g10070 | A02 | 4441673 | G | A | upstream_gene_variant | MODIFIER | c.-4012G>A| |
S67 |
3 | BAA02g10070 | A02 | 4445820 | G | A | missense_variant | MODERATE | c.136G>A|p.Gly46Ser |
S52 |
4 | BAA02g10070 | A02 | 4447348 | G | A | missense_variant | MODERATE | c.673G>A|p.Asp225Asn |
S261 |
5 | BAA02g10070 | A02 | 4447468 | G | A | missense_variant | MODERATE | c.793G>A|p.Glu265Lys |
S188 |