Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g25280 | A10 | 20500699 | G | A | missense_variant | MODERATE | c.803C>T|p.Thr268Ile |
S208 |
2 | BAA10g25280 | A10 | 20501036 | C | T | missense_variant | MODERATE | c.466G>A|p.Gly156Ser |
S89 |
3 | BAA10g25280 | A10 | 20504727 | G | A | upstream_gene_variant | MODIFIER | c.-3226C>T| |
S39 |
4 | BAA10g25280 | A10 | 20504971 | G | A | upstream_gene_variant | MODIFIER | c.-3470C>T| |
S216 |
5 | BAA10g25280 | A10 | 20505193 | C | T | upstream_gene_variant | MODIFIER | c.-3692G>A| |
S108 |
6 | BAA10g25280 | A10 | 20506349 | C | T | upstream_gene_variant | MODIFIER | c.-4848G>A| |
S8 |