Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28910 | A02 | 16324921 | G | A | upstream_gene_variant | MODIFIER | c.-4621G>A| |
S228 |
2 | BAA02g28910 | A02 | 16324978 | G | A | upstream_gene_variant | MODIFIER | c.-4564G>A| |
S71 |
3 | BAA02g28910 | A02 | 16325657 | C | T | upstream_gene_variant | MODIFIER | c.-3885C>T| |
S142 |
4 | BAA02g28910 | A02 | 16326474 | C | T | upstream_gene_variant | MODIFIER | c.-3068C>T| |
S276 |
5 | BAA02g28910 | A02 | 16326970 | G | A | upstream_gene_variant | MODIFIER | c.-2572G>A| |
S37 |
6 | BAA02g28910 | A02 | 16327853 | G | A | upstream_gene_variant | MODIFIER | c.-1689G>A| |
S187 |
7 | BAA02g28910 | A02 | 16328896 | T | G | upstream_gene_variant | MODIFIER | c.-646T>G| |
S74 |
8 | BAA02g28910 | A02 | 16329343 | C | T | upstream_gene_variant | MODIFIER | c.-199C>T| |
S77 |
9 | BAA02g28910 | A02 | 16330603 | C | T | missense_variant | MODERATE | c.395C>T|p.Ala132Val |
S115 |