Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03700 | A10 | 1783509 | G | A | missense_variant | MODERATE | c.742C>T|p.Pro248Ser |
S18 |
2 | BAA10g03700 | A10 | 1785081 | C | T | missense_variant | MODERATE | c.64G>A|p.Gly22Ser |
S19 |
3 | BAA10g03700 | A10 | 1787652 | C | T | upstream_gene_variant | MODIFIER | c.-2293G>A| |
S256 |
4 | BAA10g03700 | A10 | 1788390 | G | A | upstream_gene_variant | MODIFIER | c.-3031C>T| |
S158 |
5 | BAA10g03700 | A10 | 1790160 | G | A | upstream_gene_variant | MODIFIER | c.-4801C>T| |
S18 |