Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44760 | A02 | 36773661 | C | T | missense_variant | MODERATE | c.1079G>A|p.Cys360Tyr |
S138 |
2 | BAA02g44760 | A02 | 36773699 | C | A | missense_variant | MODERATE | c.1041G>T|p.Arg347Ser |
S171 |
3 | BAA02g44760 | A02 | 36774325 | C | T | missense_variant | MODERATE | c.415G>A|p.Asp139Asn |
S79 S84 |
4 | BAA02g44760 | A02 | 36775593 | A | G | upstream_gene_variant | MODIFIER | c.-155T>C| |
S177 |
5 | BAA02g44760 | A02 | 36775697 | G | A | upstream_gene_variant | MODIFIER | c.-259C>T| |
S291 |
6 | BAA02g44760 | A02 | 36775783 | C | T | upstream_gene_variant | MODIFIER | c.-345G>A| |
S121 |
7 | BAA02g44760 | A02 | 36776177 | G | A | upstream_gene_variant | MODIFIER | c.-739C>T| |
S229 |
8 | BAA02g44760 | A02 | 36776651 | C | T | upstream_gene_variant | MODIFIER | c.-1213G>A| |
S179 |
9 | BAA02g44760 | A02 | 36778424 | C | T | upstream_gene_variant | MODIFIER | c.-2986G>A| |
S183 S198 |
10 | BAA02g44760 | A02 | 36779548 | G | A | upstream_gene_variant | MODIFIER | c.-4110C>T| |
S25 |
11 | BAA02g44760 | A02 | 36779982 | G | A | upstream_gene_variant | MODIFIER | c.-4544C>T| |
S155 |
12 | BAA02g44760 | A02 | 36780145 | C | T | upstream_gene_variant | MODIFIER | c.-4707G>A| |
S42 |