Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10100 | A01 | 4574880 | G | A | upstream_gene_variant | MODIFIER | c.-2933G>A| |
S183 S198 |
2 | BAA01g10100 | A01 | 4575812 | C | T | upstream_gene_variant | MODIFIER | c.-2001C>T| |
S109 |
3 | BAA01g10100 | A01 | 4576940 | G | A | upstream_gene_variant | MODIFIER | c.-873G>A| |
S27 |
4 | BAA01g10100 | A01 | 4577023 | C | T | upstream_gene_variant | MODIFIER | c.-790C>T| |
S266 |
5 | BAA01g10100 | A01 | 4577498 | C | T | upstream_gene_variant | MODIFIER | c.-315C>T| |
S246 |
6 | BAA01g10100 | A01 | 4577976 | G | A | missense_variant | MODERATE | c.164G>A|p.Gly55Glu |
S179 S193 |
7 | BAA01g10100 | A01 | 4578631 | C | T | missense_variant | MODERATE | c.479C>T|p.Pro160Leu |
S42 |
8 | BAA01g10100 | A01 | 4578920 | C | T | synonymous_variant | LOW | c.678C>T|p.Phe226Phe |
S139 |
9 | BAA01g10100 | A01 | 4579700 | C | T | stop_gained | HIGH | c.982C>T|p.Gln328* |
S46 |
10 | BAA01g10100 | A01 | 4579912 | C | T | missense_variant | MODERATE | c.1106C>T|p.Ser369Phe |
S59 |
11 | BAA01g10100 | A01 | 4584842 | G | A | downstream_gene_variant | MODIFIER | c.*4002G>A| |
S273 |
12 | BAA01g10100 | A01 | 4585436 | G | A | downstream_gene_variant | MODIFIER | c.*4596G>A| |
S153 |