Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13100 | A09 | 7540349 | C | T | upstream_gene_variant | MODIFIER | c.-378C>T| |
S39 |
2 | BAA09g13100 | A09 | 7541332 | G | A | synonymous_variant | LOW | c.606G>A|p.Arg202Arg |
S60 |
3 | BAA09g13100 | A09 | 7541478 | G | A | stop_gained | HIGH | c.752G>A|p.Trp251* |
S182 |
4 | BAA09g13100 | A09 | 7541528 | C | T | missense_variant | MODERATE | c.802C>T|p.Leu268Phe |
S297 |
5 | BAA09g13100 | A09 | 7542003 | C | T | missense_variant | MODERATE | c.1277C>T|p.Pro426Leu |
S68 |
6 | BAA09g13100 | A09 | 7542034 | G | A | synonymous_variant | LOW | c.1308G>A|p.Thr436Thr |
S193 |
7 | BAA09g13100 | A09 | 7545644 | G | A | downstream_gene_variant | MODIFIER | c.*3118G>A| |
S246 |
8 | BAA09g13100 | A09 | 7547009 | G | A | downstream_gene_variant | MODIFIER | c.*4483G>A| |
S20 |