Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g04990 | A01 | 2203610 | C | T | missense_variant | MODERATE | c.902G>A|p.Ser301Asn |
S282 |
2 | BAA01g04990 | A01 | 2203876 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.723-1G>A| |
S117 |
3 | BAA01g04990 | A01 | 2205613 | C | T | missense_variant | MODERATE | c.319G>A|p.Gly107Arg |
S35 |
4 | BAA01g04990 | A01 | 2205756 | G | A | missense_variant | MODERATE | c.176C>T|p.Ser59Phe |
S259 |
5 | BAA01g04990 | A01 | 2205932 | C | T | upstream_gene_variant | MODIFIER | c.-1G>A| |
S18 |
6 | BAA01g04990 | A01 | 2208770 | G | A | upstream_gene_variant | MODIFIER | c.-2839C>T| |
S294 |
7 | BAA01g04990 | A01 | 2209999 | G | A | upstream_gene_variant | MODIFIER | c.-4068C>T| |
S108 |