Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45970 | A02 | 37498226 | C | T | missense_variant | MODERATE | c.625C>T|p.Pro209Ser |
S249 |
2 | BAA02g45970 | A02 | 37498587 | G | A | missense_variant | MODERATE | c.773G>A|p.Ser258Asn |
S132 S137 S138 S215 S237 S288 |
3 | BAA02g45970 | A02 | 37498694 | G | A | missense_variant | MODERATE | c.880G>A|p.Gly294Arg |
S247 |
4 | BAA02g45970 | A02 | 37499798 | C | T | downstream_gene_variant | MODIFIER | c.*1033C>T| |
S241 |
5 | BAA02g45970 | A02 | 37500769 | T | C | downstream_gene_variant | MODIFIER | c.*2004T>C| |
|
6 | BAA02g45970 | A02 | 37501499 | G | A | downstream_gene_variant | MODIFIER | c.*2734G>A| |
S66 |
7 | BAA02g45970 | A02 | 37501847 | C | T | downstream_gene_variant | MODIFIER | c.*3082C>T| |
S270 |
8 | BAA02g45970 | A02 | 37501926 | C | T | downstream_gene_variant | MODIFIER | c.*3161C>T| |
S181 |