Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27630 | A10 | 21471892 | C | T | missense_variant | MODERATE | c.35G>A|p.Gly12Glu |
S266 |
2 | BAA10g27630 | A10 | 21473220 | G | A | upstream_gene_variant | MODIFIER | c.-1294C>T| |
S263 |
3 | BAA10g27630 | A10 | 21476759 | G | A | upstream_gene_variant | MODIFIER | c.-4833C>T| |
S112 |
4 | BAA10g27630 | A10 | 21476839 | C | T | upstream_gene_variant | MODIFIER | c.-4913G>A| |
S242 |