Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17290 | A10 | 16715019 | G | A | missense_variant | MODERATE | c.751C>T|p.His251Tyr |
S122 |
2 | BAA10g17290 | A10 | 16719430 | G | A | upstream_gene_variant | MODIFIER | c.-3661C>T| |
S186 |
3 | BAA10g17290 | A10 | 16719665 | G | A | upstream_gene_variant | MODIFIER | c.-3896C>T| |
S180 |
4 | BAA10g17290 | A10 | 16720599 | G | A | upstream_gene_variant | MODIFIER | c.-4830C>T| |
S112 |
5 | BAA10g17290 | A10 | 16720645 | C | T | upstream_gene_variant | MODIFIER | c.-4876G>A| |
S189 |
6 | BAA10g17290 | A10 | 16720671 | C | T | upstream_gene_variant | MODIFIER | c.-4902G>A| |
S47 |