Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g44990 | A06 | 28733477 | G | A | splice_region_variant&intron_variant | LOW | c.1846-8C>T| |
S79 S91 |
2 | BAA06g44990 | A06 | 28733890 | C | T | missense_variant | MODERATE | c.1660G>A|p.Gly554Arg |
S182 |
3 | BAA06g44990 | A06 | 28735742 | C | T | missense_variant&splice_region_variant | MODERATE | c.725G>A|p.Gly242Asp |
S249 |
4 | BAA06g44990 | A06 | 28736631 | G | A | missense_variant | MODERATE | c.277C>T|p.Leu93Phe |
S152 |
5 | BAA06g44990 | A06 | 28737326 | C | T | upstream_gene_variant | MODIFIER | c.-318G>A| |
S9 |
6 | BAA06g44990 | A06 | 28737345 | C | T | upstream_gene_variant | MODIFIER | c.-337G>A| |
S80 |
7 | BAA06g44990 | A06 | 28737779 | C | T | upstream_gene_variant | MODIFIER | c.-771G>A| |
S155 |
8 | BAA06g44990 | A06 | 28739895 | C | T | upstream_gene_variant | MODIFIER | c.-2887G>A| |
S252 |
9 | BAA06g44990 | A06 | 28740214 | C | T | upstream_gene_variant | MODIFIER | c.-3206G>A| |
S274 |