Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28770 | A01 | 18075167 | C | T | missense_variant | MODERATE | c.1423C>T|p.Pro475Ser |
S271 |
2 | BAA01g28770 | A01 | 18075191 | G | A | missense_variant | MODERATE | c.1447G>A|p.Asp483Asn |
S218 |
3 | BAA01g28770 | A01 | 18075773 | G | A | missense_variant | MODERATE | c.1961G>A|p.Arg654His |
S294 |
4 | BAA01g28770 | A01 | 18075883 | G | A | missense_variant | MODERATE | c.2071G>A|p.Ala691Thr |
S281 |
5 | BAA01g28770 | A01 | 18080302 | G | A | downstream_gene_variant | MODIFIER | c.*224G>A| |
S197 |