Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16690 | A01 | 8129972 | C | T | upstream_gene_variant | MODIFIER | c.-1814C>T| |
S48 |
2 | BAA01g16690 | A01 | 8130454 | C | T | upstream_gene_variant | MODIFIER | c.-1332C>T| |
S62 |
3 | BAA01g16690 | A01 | 8131562 | G | A | upstream_gene_variant | MODIFIER | c.-224G>A| |
S296 |
4 | BAA01g16690 | A01 | 8132309 | C | T | missense_variant | MODERATE | c.347C>T|p.Ala116Val |
S206 |
5 | BAA01g16690 | A01 | 8132873 | G | A | missense_variant | MODERATE | c.911G>A|p.Gly304Glu |
S37 |
6 | BAA01g16690 | A01 | 8133011 | C | T | missense_variant | MODERATE | c.1049C>T|p.Ala350Val |
S19 |
7 | BAA01g16690 | A01 | 8133587 | C | T | missense_variant | MODERATE | c.1625C>T|p.Ser542Phe |
S68 |
8 | BAA01g16690 | A01 | 8133625 | G | A | missense_variant | MODERATE | c.1663G>A|p.Val555Ile |
S274 |
9 | BAA01g16690 | A01 | 8133704 | G | A | stop_gained | HIGH | c.1742G>A|p.Trp581* |
S256 |
10 | BAA01g16690 | A01 | 8133769 | G | A | missense_variant | MODERATE | c.1807G>A|p.Val603Met |
S301 S304 |
11 | BAA01g16690 | A01 | 8135958 | G | A | downstream_gene_variant | MODIFIER | c.*1863G>A| |
S224 |