Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09680 | A02 | 4260178 | C | T | splice_region_variant&intron_variant | LOW | c.259+8C>T| |
S58 |
2 | BAA02g09680 | A02 | 4260416 | G | A | missense_variant | MODERATE | c.343G>A|p.Asp115Asn |
S41 |
3 | BAA02g09680 | A02 | 4260419 | C | T | missense_variant | MODERATE | c.346C>T|p.Pro116Ser |
S9 |
4 | BAA02g09680 | A02 | 4260768 | C | T | synonymous_variant | LOW | c.534C>T|p.Arg178Arg |
S71 |
5 | BAA02g09680 | A02 | 4261220 | C | T | synonymous_variant | LOW | c.915C>T|p.Phe305Phe |
S224 |
6 | BAA02g09680 | A02 | 4261659 | C | T | missense_variant | MODERATE | c.1354C>T|p.Leu452Phe |
S193 |
7 | BAA02g09680 | A02 | 4265317 | C | T | downstream_gene_variant | MODIFIER | c.*3566C>T| |
S1 S90 |
8 | BAA02g09680 | A02 | 4265529 | C | T | downstream_gene_variant | MODIFIER | c.*3778C>T| |
S219 |
9 | BAA02g09680 | A02 | 4265700 | A | T | downstream_gene_variant | MODIFIER | c.*3949A>T| |
S84 S93 |