Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28960 | A02 | 16429526 | G | A | missense_variant | MODERATE | c.2612C>T|p.Ser871Phe |
S68 |
2 | BAA02g28960 | A02 | 16429977 | C | T | missense_variant | MODERATE | c.2161G>A|p.Glu721Lys |
S157 S163 |
3 | BAA02g28960 | A02 | 16430401 | G | A | synonymous_variant | LOW | c.1737C>T|p.Tyr579Tyr |
S295 |
4 | BAA02g28960 | A02 | 16430882 | C | T | stop_gained | HIGH | c.1256G>A|p.Trp419* |
S281 |
5 | BAA02g28960 | A02 | 16432445 | G | A | synonymous_variant | LOW | c.612C>T|p.Asn204Asn |
S116 |
6 | BAA02g28960 | A02 | 16433068 | C | T | missense_variant | MODERATE | c.403G>A|p.Ala135Thr |
S67 |
7 | BAA02g28960 | A02 | 16433576 | C | T | synonymous_variant | LOW | c.186G>A|p.Lys62Lys |
S287 |
8 | BAA02g28960 | A02 | 16434436 | G | A | upstream_gene_variant | MODIFIER | c.-437C>T| |
S17 |
9 | BAA02g28960 | A02 | 16434676 | C | T | upstream_gene_variant | MODIFIER | c.-677G>A| |
S247 |
10 | BAA02g28960 | A02 | 16434684 | G | A | upstream_gene_variant | MODIFIER | c.-685C>T| |
S55 |
11 | BAA02g28960 | A02 | 16434690 | G | A | upstream_gene_variant | MODIFIER | c.-691C>T| |
S122 S279 |
12 | BAA02g28960 | A02 | 16434789 | G | A | upstream_gene_variant | MODIFIER | c.-790C>T| |
S47 |
13 | BAA02g28960 | A02 | 16435144 | G | A | upstream_gene_variant | MODIFIER | c.-1145C>T| |
S25 |
14 | BAA02g28960 | A02 | 16438746 | G | A | upstream_gene_variant | MODIFIER | c.-4747C>T| |
S188 |