Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27690 | A10 | 21492697 | C | T | upstream_gene_variant | MODIFIER | c.-4720C>T| |
S277 |
2 | BAA10g27690 | A10 | 21497908 | G | A | synonymous_variant | LOW | c.492G>A|p.Ala164Ala |
S122 |
3 | BAA10g27690 | A10 | 21498439 | C | T | synonymous_variant | LOW | c.1023C>T|p.Ser341Ser |
S36 |