Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00770 | A02 | 376312 | C | T | missense_variant | MODERATE | c.1070G>A|p.Ser357Asn |
S1 S90 |
2 | BAA02g00770 | A02 | 376428 | C | T | missense_variant | MODERATE | c.1019G>A|p.Gly340Glu |
S306 S308 |
3 | BAA02g00770 | A02 | 377201 | G | A | missense_variant | MODERATE | c.643C>T|p.Pro215Ser |
S163 |
4 | BAA02g00770 | A02 | 377420 | C | T | missense_variant | MODERATE | c.505G>A|p.Ala169Thr |
S133 |
5 | BAA02g00770 | A02 | 380730 | C | T | upstream_gene_variant | MODIFIER | c.-2499G>A| |
S178 |
6 | BAA02g00770 | A02 | 380775 | G | A | upstream_gene_variant | MODIFIER | c.-2544C>T| |
S17 |