Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19460 | A10 | 17828659 | C | T | upstream_gene_variant | MODIFIER | c.-4956C>T| |
S212 |
2 | BAA10g19460 | A10 | 17833816 | C | T | missense_variant | MODERATE | c.202C>T|p.Pro68Ser |
S277 |
3 | BAA10g19460 | A10 | 17834046 | C | T | synonymous_variant | LOW | c.432C>T|p.Asn144Asn |
S11 |