Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g12000 | A08 | 10539023 | C | T | missense_variant | MODERATE | c.163G>A|p.Asp55Asn |
S276 |
2 | BAA08g12000 | A08 | 10542730 | G | A | upstream_gene_variant | MODIFIER | c.-3545C>T| |
S279 |
3 | BAA08g12000 | A08 | 10544046 | C | T | upstream_gene_variant | MODIFIER | c.-4861G>A| |
S113 |
4 | BAA08g12000 | A08 | 10544051 | C | T | upstream_gene_variant | MODIFIER | c.-4866G>A| |
S201 |