Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00760 | A10 | 358420 | C | T | missense_variant | MODERATE | c.598G>A|p.Gly200Arg |
S263 |
2 | BAA10g00760 | A10 | 358954 | G | A | missense_variant | MODERATE | c.247C>T|p.Pro83Ser |
S280 |
3 | BAA10g00760 | A10 | 359960 | G | A | upstream_gene_variant | MODIFIER | c.-505C>T| |
S136 |
4 | BAA10g00760 | A10 | 363196 | C | T | upstream_gene_variant | MODIFIER | c.-3741G>A| |
S294 |
5 | BAA10g00760 | A10 | 364203 | T | C | upstream_gene_variant | MODIFIER | c.-4748A>G| |
S138 |