Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19140 | A10 | 17677363 | C | T | upstream_gene_variant | MODIFIER | c.-174C>T| |
S72 |
2 | BAA10g19140 | A10 | 17677504 | G | A | upstream_gene_variant | MODIFIER | c.-33G>A| |
S292 |
3 | BAA10g19140 | A10 | 17677585 | C | T | missense_variant | MODERATE | c.49C>T|p.Arg17Trp |
S283 |
4 | BAA10g19140 | A10 | 17677593 | C | T | synonymous_variant | LOW | c.57C>T|p.Ala19Ala |
S298 |