Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00690 | A10 | 335125 | G | A | missense_variant | MODERATE | c.586C>T|p.Pro196Ser |
S156 |
2 | BAA10g00690 | A10 | 335297 | G | A | synonymous_variant | LOW | c.414C>T|p.Asp138Asp |
S180 |
3 | BAA10g00690 | A10 | 336213 | G | A | upstream_gene_variant | MODIFIER | c.-503C>T| |
S16 |
4 | BAA10g00690 | A10 | 338358 | G | A | upstream_gene_variant | MODIFIER | c.-2648C>T| |
S158 |
5 | BAA10g00690 | A10 | 339316 | G | A | upstream_gene_variant | MODIFIER | c.-3606C>T| |
S134 |