Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15660 | A01 | 7610874 | C | T | upstream_gene_variant | MODIFIER | c.-1303C>T| |
S49 |
2 | BAA01g15660 | A01 | 7612171 | C | T | upstream_gene_variant | MODIFIER | c.-6C>T| |
S122 |
3 | BAA01g15660 | A01 | 7612909 | G | A | synonymous_variant | LOW | c.513G>A|p.Ala171Ala |
S183 |
4 | BAA01g15660 | A01 | 7613647 | G | A | missense_variant | MODERATE | c.1009G>A|p.Glu337Lys |
S297 |
5 | BAA01g15660 | A01 | 7613667 | C | T | synonymous_variant | LOW | c.1029C>T|p.Leu343Leu |
S153 |
6 | BAA01g15660 | A01 | 7613829 | C | T | missense_variant | MODERATE | c.1103C>T|p.Thr368Ile |
S107 |