Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g42170 | A01 | 28004043 | G | A | missense_variant | MODERATE | c.636G>A|p.Met212Ile |
S284 |
2 | BAA01g42170 | A01 | 28004190 | G | A | splice_region_variant&synonymous_variant | LOW | c.783G>A|p.Lys261Lys |
S223 |
3 | BAA01g42170 | A01 | 28004781 | C | T | synonymous_variant | LOW | c.873C>T|p.Ile291Ile |
S201 |
4 | BAA01g42170 | A01 | 28004878 | G | A | missense_variant | MODERATE | c.970G>A|p.Glu324Lys |
S197 |
5 | BAA01g42170 | A01 | 28005740 | C | T | missense_variant | MODERATE | c.1499C>T|p.Ala500Val |
S130 |
6 | BAA01g42170 | A01 | 28006686 | G | A | downstream_gene_variant | MODIFIER | c.*603G>A| |
S70 |
7 | BAA01g42170 | A01 | 28008156 | C | T | downstream_gene_variant | MODIFIER | c.*2073C>T| |
S162 |
8 | BAA01g42170 | A01 | 28008562 | G | A | downstream_gene_variant | MODIFIER | c.*2479G>A| |
S251 |