Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g31100 | A05 | 33942746 | C | T | stop_gained | HIGH | c.711G>A|p.Trp237* |
S128 |
2 | BAA05g31100 | A05 | 33943044 | G | A | missense_variant | MODERATE | c.413C>T|p.Ala138Val |
S41 |
3 | BAA05g31100 | A05 | 33943128 | G | A | missense_variant | MODERATE | c.329C>T|p.Ser110Phe |
S122 |
4 | BAA05g31100 | A05 | 33943289 | C | T | synonymous_variant | LOW | c.168G>A|p.Lys56Lys |
S148 S30 S31 |
5 | BAA05g31100 | A05 | 33943376 | G | A | synonymous_variant | LOW | c.81C>T|p.His27His |
S150 |
6 | BAA05g31100 | A05 | 33943416 | G | A | missense_variant | MODERATE | c.41C>T|p.Ser14Phe |
S256 |
7 | BAA05g31100 | A05 | 33944578 | C | T | upstream_gene_variant | MODIFIER | c.-1122G>A| |
S135 |
8 | BAA05g31100 | A05 | 33945371 | G | A | upstream_gene_variant | MODIFIER | c.-1915C>T| |
S296 |
9 | BAA05g31100 | A05 | 33947672 | C | T | upstream_gene_variant | MODIFIER | c.-4216G>A| |
S146 |