Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43980 | A02 | 36299024 | C | T | upstream_gene_variant | MODIFIER | c.-3000C>T| |
S208 S219 |
2 | BAA02g43980 | A02 | 36303607 | C | T | missense_variant | MODERATE | c.902C>T|p.Ser301Phe |
S130 |
3 | BAA02g43980 | A02 | 36303730 | G | A | missense_variant | MODERATE | c.1025G>A|p.Arg342Lys |
S57 |
4 | BAA02g43980 | A02 | 36304438 | G | A | stop_gained | HIGH | c.1449G>A|p.Trp483* |
S302 |
5 | BAA02g43980 | A02 | 36304557 | C | T | missense_variant | MODERATE | c.1568C>T|p.Pro523Leu |
S133 |
6 | BAA02g43980 | A02 | 36306729 | G | A | intron_variant | MODIFIER | c.1844+313G>A| |
S156 |
7 | BAA02g43980 | A02 | 36307671 | C | T | intron_variant | MODIFIER | c.1845-92C>T| |
S257 |
8 | BAA02g43980 | A02 | 36307693 | G | A | intron_variant | MODIFIER | c.1845-70G>A| |
S84 S93 |
9 | BAA02g43980 | A02 | 36308166 | G | A | downstream_gene_variant | MODIFIER | c.*322G>A| |
S164 |
10 | BAA02g43980 | A02 | 36311506 | C | T | downstream_gene_variant | MODIFIER | c.*3662C>T| |
S249 |