Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19700 | A02 | 10260975 | C | T | synonymous_variant | LOW | c.822G>A|p.Ala274Ala |
S80 |
2 | BAA02g19700 | A02 | 10261308 | G | A | synonymous_variant | LOW | c.489C>T|p.Val163Val |
S34 |
3 | BAA02g19700 | A02 | 10261397 | C | T | missense_variant | MODERATE | c.400G>A|p.Asp134Asn |
S46 |
4 | BAA02g19700 | A02 | 10261451 | G | A | missense_variant | MODERATE | c.346C>T|p.Pro116Ser |
S174 S27 |
5 | BAA02g19700 | A02 | 10262893 | C | T | upstream_gene_variant | MODIFIER | c.-1097G>A| |
S171 |
6 | BAA02g19700 | A02 | 10262908 | C | T | upstream_gene_variant | MODIFIER | c.-1112G>A| |
S279 |
7 | BAA02g19700 | A02 | 10263354 | C | T | upstream_gene_variant | MODIFIER | c.-1558G>A| |
S49 |
8 | BAA02g19700 | A02 | 10264612 | C | T | upstream_gene_variant | MODIFIER | c.-2816G>A| |
S119 |
9 | BAA02g19700 | A02 | 10265401 | G | A | upstream_gene_variant | MODIFIER | c.-3605C>T| |
S256 |
10 | BAA02g19700 | A02 | 10266321 | C | T | upstream_gene_variant | MODIFIER | c.-4525G>A| |
S58 |