Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01970 | A02 | 881321 | G | A | upstream_gene_variant | MODIFIER | c.-547G>A| |
S237 |
2 | BAA02g01970 | A02 | 881332 | C | T | upstream_gene_variant | MODIFIER | c.-536C>T| |
S178 |
3 | BAA02g01970 | A02 | 881413 | C | T | upstream_gene_variant | MODIFIER | c.-455C>T| |
S216 |
4 | BAA02g01970 | A02 | 881465 | C | T | upstream_gene_variant | MODIFIER | c.-403C>T| |
S34 |
5 | BAA02g01970 | A02 | 881502 | C | T | upstream_gene_variant | MODIFIER | c.-366C>T| |
S195 |
6 | BAA02g01970 | A02 | 881830 | G | A | upstream_gene_variant | MODIFIER | c.-38G>A| |
S208 |
7 | BAA02g01970 | A02 | 882728 | C | T | missense_variant | MODERATE | c.421C>T|p.Pro141Ser |
S274 |
8 | BAA02g01970 | A02 | 883704 | G | A | missense_variant | MODERATE | c.827G>A|p.Ser276Asn |
S48 |
9 | BAA02g01970 | A02 | 887136 | G | A | downstream_gene_variant | MODIFIER | c.*3246G>A| |
S256 |
10 | BAA02g01970 | A02 | 888124 | G | A | downstream_gene_variant | MODIFIER | c.*4234G>A| |
S23 |