Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17770 | A05 | 10060470 | G | A | missense_variant | MODERATE | c.728G>A|p.Arg243Lys |
S219 |
2 | BAA05g17770 | A05 | 10061108 | C | T | downstream_gene_variant | MODIFIER | c.*232C>T| |
S99 |
3 | BAA05g17770 | A05 | 10061122 | C | T | downstream_gene_variant | MODIFIER | c.*246C>T| |
S149 |
4 | BAA05g17770 | A05 | 10061566 | C | T | downstream_gene_variant | MODIFIER | c.*690C>T| |
S182 |
5 | BAA05g17770 | A05 | 10061737 | G | A | downstream_gene_variant | MODIFIER | c.*861G>A| |
S11 |
6 | BAA05g17770 | A05 | 10061753 | G | A | downstream_gene_variant | MODIFIER | c.*877G>A| |
S218 |
7 | BAA05g17770 | A05 | 10061791 | C | T | downstream_gene_variant | MODIFIER | c.*915C>T| |
S216 |
8 | BAA05g17770 | A05 | 10061938 | C | T | downstream_gene_variant | MODIFIER | c.*1062C>T| |
S261 |
9 | BAA05g17770 | A05 | 10061998 | G | A | downstream_gene_variant | MODIFIER | c.*1122G>A| |
S278 |