Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g05380 | A09 | 3092781 | C | T | missense_variant | MODERATE | c.220G>A|p.Ala74Thr |
S13 |
2 | BAA09g05380 | A09 | 3092797 | G | A | splice_region_variant&synonymous_variant | LOW | c.204C>T|p.Val68Val |
S277 |
3 | BAA09g05380 | A09 | 3093825 | C | T | upstream_gene_variant | MODIFIER | c.-462G>A| |
S95 |
4 | BAA09g05380 | A09 | 3094978 | G | A | upstream_gene_variant | MODIFIER | c.-1615C>T| |
S165 |
5 | BAA09g05380 | A09 | 3097218 | C | T | upstream_gene_variant | MODIFIER | c.-3855G>A| |
S133 |