Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20990 | A02 | 11218688 | C | T | upstream_gene_variant | MODIFIER | c.-3509C>T| |
S308 |
2 | BAA02g20990 | A02 | 11218817 | G | A | upstream_gene_variant | MODIFIER | c.-3380G>A| |
S269 |
3 | BAA02g20990 | A02 | 11219470 | A | T | upstream_gene_variant | MODIFIER | c.-2727A>T| |
S249 |
4 | BAA02g20990 | A02 | 11220116 | G | A | upstream_gene_variant | MODIFIER | c.-2081G>A| |
S282 |
5 | BAA02g20990 | A02 | 11220476 | G | A | upstream_gene_variant | MODIFIER | c.-1721G>A| |
S297 |
6 | BAA02g20990 | A02 | 11223824 | C | T | missense_variant | MODERATE | c.1091C>T|p.Ser364Phe |
S155 S211 |