Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46000 | A02 | 37511077 | C | T | synonymous_variant | LOW | c.108C>T|p.Ala36Ala |
S42 |
2 | BAA02g46000 | A02 | 37511183 | G | A | missense_variant | MODERATE | c.214G>A|p.Asp72Asn |
S202 |
3 | BAA02g46000 | A02 | 37511944 | G | A | missense_variant | MODERATE | c.535G>A|p.Ala179Thr |
S37 |
4 | BAA02g46000 | A02 | 37512324 | C | T | missense_variant | MODERATE | c.670C>T|p.Pro224Ser |
S33 |
5 | BAA02g46000 | A02 | 37515073 | C | T | downstream_gene_variant | MODIFIER | c.*2467C>T| |
S193 |
6 | BAA02g46000 | A02 | 37515298 | T | C | downstream_gene_variant | MODIFIER | c.*2692T>C| |
S202 |
7 | BAA02g46000 | A02 | 37515538 | C | T | downstream_gene_variant | MODIFIER | c.*2932C>T| |
S47 |
8 | BAA02g46000 | A02 | 37515556 | C | T | downstream_gene_variant | MODIFIER | c.*2950C>T| |
S64 |