Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27990 | A02 | 15765452 | C | T | missense_variant | MODERATE | c.1055G>A|p.Cys352Tyr |
S299 |
2 | BAA02g27990 | A02 | 15765693 | C | T | missense_variant | MODERATE | c.901G>A|p.Gly301Arg |
S177 |
3 | BAA02g27990 | A02 | 15765714 | C | T | missense_variant | MODERATE | c.880G>A|p.Glu294Lys |
S8 |
4 | BAA02g27990 | A02 | 15766256 | C | T | missense_variant | MODERATE | c.503G>A|p.Ser168Asn |
S308 |
5 | BAA02g27990 | A02 | 15766359 | C | T | missense_variant | MODERATE | c.400G>A|p.Val134Ile |
S87 |
6 | BAA02g27990 | A02 | 15766395 | C | T | missense_variant | MODERATE | c.364G>A|p.Asp122Asn |
S250 |
7 | BAA02g27990 | A02 | 15766404 | G | A | missense_variant | MODERATE | c.355C>T|p.Leu119Phe |
S19 |
8 | BAA02g27990 | A02 | 15766485 | G | A | missense_variant | MODERATE | c.274C>T|p.Pro92Ser |
S116 |
9 | BAA02g27990 | A02 | 15766605 | G | A | missense_variant | MODERATE | c.154C>T|p.Pro52Ser |
S261 |
10 | BAA02g27990 | A02 | 15768996 | G | A | upstream_gene_variant | MODIFIER | c.-2238C>T| |
S251 |
11 | BAA02g27990 | A02 | 15771538 | G | A | upstream_gene_variant | MODIFIER | c.-4780C>T| |
S247 |