Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00690 | A09 | 599717 | C | T | missense_variant | MODERATE | c.263G>A|p.Gly88Glu |
S35 |
2 | BAA09g00690 | A09 | 600004 | G | A | missense_variant | MODERATE | c.53C>T|p.Pro18Leu |
S148 S210 |
3 | BAA09g00690 | A09 | 604078 | C | T | upstream_gene_variant | MODIFIER | c.-4022G>A| |
S59 |
4 | BAA09g00690 | A09 | 604924 | C | T | upstream_gene_variant | MODIFIER | c.-4868G>A| |
S70 |