Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00660 | A02 | 343104 | C | T | missense_variant | MODERATE | c.1075G>A|p.Val359Ile |
S186 |
2 | BAA02g00660 | A02 | 343755 | C | T | stop_gained | HIGH | c.504G>A|p.Trp168* |
S131 |
3 | BAA02g00660 | A02 | 343979 | G | A | missense_variant | MODERATE | c.367C>T|p.His123Tyr |
S202 |
4 | BAA02g00660 | A02 | 344892 | G | A | missense_variant | MODERATE | c.41C>T|p.Thr14Ile |
S293 |
5 | BAA02g00660 | A02 | 345316 | G | A | upstream_gene_variant | MODIFIER | c.-384C>T| |
S289 S290 |
6 | BAA02g00660 | A02 | 345891 | G | A | upstream_gene_variant | MODIFIER | c.-959C>T| |
S105 S106 |
7 | BAA02g00660 | A02 | 348175 | C | T | upstream_gene_variant | MODIFIER | c.-3243G>A| |
S167 |
8 | BAA02g00660 | A02 | 348496 | G | A | upstream_gene_variant | MODIFIER | c.-3564C>T| |
S96 |
9 | BAA02g00660 | A02 | 349861 | G | A | upstream_gene_variant | MODIFIER | c.-4929C>T| |
S161 |
10 | BAA02g00660 | A02 | 349925 | C | T | upstream_gene_variant | MODIFIER | c.-4993G>A| |
S150 |