Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26230 | A09 | 17003403 | C | T | missense_variant | MODERATE | c.1165G>A|p.Asp389Asn |
S82 S92 |
2 | BAA09g26230 | A09 | 17003404 | G | A | synonymous_variant | LOW | c.1164C>T|p.Ser388Ser |
S259 |
3 | BAA09g26230 | A09 | 17003450 | C | T | missense_variant | MODERATE | c.1118G>A|p.Gly373Glu |
S40 |
4 | BAA09g26230 | A09 | 17004021 | G | A | missense_variant | MODERATE | c.547C>T|p.Pro183Ser |
S56 |
5 | BAA09g26230 | A09 | 17007419 | G | T | upstream_gene_variant | MODIFIER | c.-2852C>A| |
S133 S150 S172 |
6 | BAA09g26230 | A09 | 17007485 | C | T | upstream_gene_variant | MODIFIER | c.-2918G>A| |
S23 |
7 | BAA09g26230 | A09 | 17009289 | C | T | upstream_gene_variant | MODIFIER | c.-4722G>A| |
S278 |