Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14860 | A02 | 7020844 | C | T | upstream_gene_variant | MODIFIER | c.-991C>T| |
S87 |
2 | BAA02g14860 | A02 | 7021759 | C | T | upstream_gene_variant | MODIFIER | c.-76C>T| |
S261 |
3 | BAA02g14860 | A02 | 7023360 | G | A | synonymous_variant | LOW | c.1089G>A|p.Arg363Arg |
S168 |
4 | BAA02g14860 | A02 | 7023452 | T | G | missense_variant | MODERATE | c.1181T>G|p.Ile394Ser |
S15 S186 S215 S230 S234 S41 |
5 | BAA02g14860 | A02 | 7024280 | G | A | downstream_gene_variant | MODIFIER | c.*587G>A| |
S251 |
6 | BAA02g14860 | A02 | 7024579 | C | T | downstream_gene_variant | MODIFIER | c.*886C>T| |
S78 S83 |
7 | BAA02g14860 | A02 | 7026101 | G | A | downstream_gene_variant | MODIFIER | c.*2408G>A| |
S10 |
8 | BAA02g14860 | A02 | 7026601 | C | T | downstream_gene_variant | MODIFIER | c.*2908C>T| |
S115 |
9 | BAA02g14860 | A02 | 7026729 | C | T | downstream_gene_variant | MODIFIER | c.*3036C>T| |
S230 |
10 | BAA02g14860 | A02 | 7026766 | C | T | downstream_gene_variant | MODIFIER | c.*3073C>T| |
S267 |