Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g52150 | A03 | 25484790 | C | T | missense_variant | MODERATE | c.109C>T|p.Leu37Phe |
S58 |
2 | BAA03g52150 | A03 | 25485421 | G | A | missense_variant | MODERATE | c.740G>A|p.Arg247Lys |
S230 |
3 | BAA03g52150 | A03 | 25485925 | G | A | missense_variant | MODERATE | c.1244G>A|p.Gly415Glu |
S168 |
4 | BAA03g52150 | A03 | 25486062 | C | T | missense_variant | MODERATE | c.1381C>T|p.Leu461Phe |
S188 S276 S298 |
5 | BAA03g52150 | A03 | 25486078 | G | A | missense_variant | MODERATE | c.1397G>A|p.Gly466Glu |
S56 |
6 | BAA03g52150 | A03 | 25490510 | G | A | downstream_gene_variant | MODIFIER | c.*4278G>A| |
S256 |
7 | BAA03g52150 | A03 | 25490725 | G | A | downstream_gene_variant | MODIFIER | c.*4493G>A| |
S6 |
8 | BAA03g52150 | A03 | 25490765 | C | T | downstream_gene_variant | MODIFIER | c.*4533C>T| |
S296 |
9 | BAA03g52150 | A03 | 25491012 | C | T | downstream_gene_variant | MODIFIER | c.*4780C>T| |
S35 |