Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g47910 | A03 | 23021646 | C | T | upstream_gene_variant | MODIFIER | c.-1377C>T| |
S99 |
2 | BAA03g47910 | A03 | 23021725 | C | T | upstream_gene_variant | MODIFIER | c.-1298C>T| |
S113 |
3 | BAA03g47910 | A03 | 23021815 | C | T | upstream_gene_variant | MODIFIER | c.-1208C>T| |
S241 |
4 | BAA03g47910 | A03 | 23022097 | C | T | upstream_gene_variant | MODIFIER | c.-926C>T| |
S229 |
5 | BAA03g47910 | A03 | 23023254 | C | T | intron_variant | MODIFIER | c.121-14C>T| |
S192 |
6 | BAA03g47910 | A03 | 23023481 | C | T | synonymous_variant | LOW | c.216C>T|p.Ile72Ile |
S293 |
7 | BAA03g47910 | A03 | 23024329 | C | T | intron_variant | MODIFIER | c.289+775C>T| |
S18 |
8 | BAA03g47910 | A03 | 23024765 | C | T | intron_variant | MODIFIER | c.290-473C>T| |
S82 S92 |
9 | BAA03g47910 | A03 | 23025276 | C | T | missense_variant | MODERATE | c.328C>T|p.Pro110Ser |
S296 |
10 | BAA03g47910 | A03 | 23025674 | G | A | synonymous_variant | LOW | c.576G>A|p.Pro192Pro |
S42 |