Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14110 | A02 | 6616768 | G | A | missense_variant | MODERATE | c.584G>A|p.Arg195Lys |
S298 |
2 | BAA02g14110 | A02 | 6616786 | G | A | missense_variant | MODERATE | c.602G>A|p.Gly201Glu |
S191 |
3 | BAA02g14110 | A02 | 6616872 | G | A | missense_variant | MODERATE | c.688G>A|p.Asp230Asn |
S35 |
4 | BAA02g14110 | A02 | 6617022 | C | T | synonymous_variant | LOW | c.747C>T|p.Asn249Asn |
S13 |
5 | BAA02g14110 | A02 | 6621163 | C | T | downstream_gene_variant | MODIFIER | c.*4138C>T| |
S124 |
6 | BAA02g14110 | A02 | 6621702 | G | A | downstream_gene_variant | MODIFIER | c.*4677G>A| |
S282 |