Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00610 | A10 | 295560 | C | T | missense_variant | MODERATE | c.766G>A|p.Asp256Asn |
S188 |
2 | BAA10g00610 | A10 | 295813 | G | A | synonymous_variant | LOW | c.513C>T|p.Ile171Ile |
S5 |
3 | BAA10g00610 | A10 | 297522 | C | T | upstream_gene_variant | MODIFIER | c.-1099G>A| |
S166 |
4 | BAA10g00610 | A10 | 299104 | C | T | upstream_gene_variant | MODIFIER | c.-2681G>A| |
S54 |
5 | BAA10g00610 | A10 | 300451 | G | A | upstream_gene_variant | MODIFIER | c.-4028C>T| |
S80 |