Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g34140 | A01 | 22818073 | C | T | upstream_gene_variant | MODIFIER | c.-623C>T| |
S249 |
2 | BAA01g34140 | A01 | 22818719 | G | A | splice_region_variant&intron_variant | LOW | c.16+8G>A| |
S144 |
3 | BAA01g34140 | A01 | 22820625 | G | A | missense_variant | MODERATE | c.1508G>A|p.Gly503Asp |
S60 |
4 | BAA01g34140 | A01 | 22820936 | T | C | synonymous_variant | LOW | c.1722T>C|p.Asn574Asn |
S75 |
5 | BAA01g34140 | A01 | 22820967 | G | A | missense_variant | MODERATE | c.1753G>A|p.Gly585Ser |
S263 |
6 | BAA01g34140 | A01 | 22822187 | C | T | downstream_gene_variant | MODIFIER | c.*1119C>T| |
S79 S84 |
7 | BAA01g34140 | A01 | 22822835 | C | T | downstream_gene_variant | MODIFIER | c.*1767C>T| |
S162 |
8 | BAA01g34140 | A01 | 22822852 | C | T | downstream_gene_variant | MODIFIER | c.*1784C>T| |
S200 |
9 | BAA01g34140 | A01 | 22826005 | G | A | downstream_gene_variant | MODIFIER | c.*4937G>A| |
S135 S221 |