Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12130 | A02 | 5474070 | G | A | upstream_gene_variant | MODIFIER | c.-2992G>A| |
S52 |
2 | BAA02g12130 | A02 | 5474876 | C | T | upstream_gene_variant | MODIFIER | c.-2186C>T| |
S274 |
3 | BAA02g12130 | A02 | 5475106 | G | A | upstream_gene_variant | MODIFIER | c.-1956G>A| |
S161 |
4 | BAA02g12130 | A02 | 5475480 | C | T | upstream_gene_variant | MODIFIER | c.-1582C>T| |
S234 |
5 | BAA02g12130 | A02 | 5475616 | C | T | upstream_gene_variant | MODIFIER | c.-1446C>T| |
S181 |
6 | BAA02g12130 | A02 | 5475723 | C | T | upstream_gene_variant | MODIFIER | c.-1339C>T| |
S144 |
7 | BAA02g12130 | A02 | 5477399 | C | T | missense_variant | MODERATE | c.250C>T|p.Arg84Cys |
S299 |
8 | BAA02g12130 | A02 | 5477889 | C | T | missense_variant | MODERATE | c.506C>T|p.Thr169Ile |
S216 |
9 | BAA02g12130 | A02 | 5478513 | C | T | missense_variant | MODERATE | c.911C>T|p.Thr304Ile |
S224 |