Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g10660 | A04 | 16739791 | C | T | missense_variant | MODERATE | c.190G>A|p.Asp64Asn |
S20 |
2 | BAA04g10660 | A04 | 16740257 | G | A | upstream_gene_variant | MODIFIER | c.-277C>T| |
S219 S72 |
3 | BAA04g10660 | A04 | 16740385 | C | T | upstream_gene_variant | MODIFIER | c.-405G>A| |
S302 |
4 | BAA04g10660 | A04 | 16742076 | A | T | upstream_gene_variant | MODIFIER | c.-2096T>A| |
S174 |
5 | BAA04g10660 | A04 | 16742498 | C | T | upstream_gene_variant | MODIFIER | c.-2518G>A| |
S267 |
6 | BAA04g10660 | A04 | 16744267 | C | T | upstream_gene_variant | MODIFIER | c.-4287G>A| |
S156 |
7 | BAA04g10660 | A04 | 16744611 | G | A | upstream_gene_variant | MODIFIER | c.-4631C>T| |
S125 |
8 | BAA04g10660 | A04 | 16744666 | C | T | upstream_gene_variant | MODIFIER | c.-4686G>A| |
S135 |