Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15500 | A02 | 7480097 | G | A | missense_variant | MODERATE | c.869C>T|p.Thr290Ile |
S172 S217 |
2 | BAA02g15500 | A02 | 7480553 | C | T | missense_variant | MODERATE | c.413G>A|p.Gly138Asp |
S6 |
3 | BAA02g15500 | A02 | 7484529 | C | T | upstream_gene_variant | MODIFIER | c.-3478G>A| |
S284 |
4 | BAA02g15500 | A02 | 7485246 | C | T | upstream_gene_variant | MODIFIER | c.-4195G>A| |
S267 |
5 | BAA02g15500 | A02 | 7485529 | G | A | upstream_gene_variant | MODIFIER | c.-4478C>T| |
S231 |
6 | BAA02g15500 | A02 | 7485666 | C | T | upstream_gene_variant | MODIFIER | c.-4615G>A| |
S180 |
7 | BAA02g15500 | A02 | 7485917 | G | A | upstream_gene_variant | MODIFIER | c.-4866C>T| |
S190 |