Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g61450 | A09 | 58490670 | C | T | missense_variant | MODERATE | c.2152G>A|p.Asp718Asn |
S33 |
2 | BAA09g61450 | A09 | 58492433 | C | T | missense_variant | MODERATE | c.998G>A|p.Gly333Glu |
S13 |
3 | BAA09g61450 | A09 | 58492830 | C | T | missense_variant | MODERATE | c.769G>A|p.Glu257Lys |
S20 |
4 | BAA09g61450 | A09 | 58492930 | G | A | synonymous_variant | LOW | c.669C>T|p.Ser223Ser |
S128 |
5 | BAA09g61450 | A09 | 58493143 | C | T | missense_variant | MODERATE | c.529G>A|p.Glu177Lys |
S75 S81 |
6 | BAA09g61450 | A09 | 58494033 | G | A | missense_variant&splice_region_variant | MODERATE | c.106C>T|p.His36Tyr |
S202 |
7 | BAA09g61450 | A09 | 58494826 | C | T | upstream_gene_variant | MODIFIER | c.-688G>A| |
S272 |
8 | BAA09g61450 | A09 | 58496577 | C | T | upstream_gene_variant | MODIFIER | c.-2439G>A| |
S208 S219 |
9 | BAA09g61450 | A09 | 58497889 | C | T | upstream_gene_variant | MODIFIER | c.-3751G>A| |
S223 |