Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g09060 | A09 | 5042404 | C | T | upstream_gene_variant | MODIFIER | c.-929C>T| |
S217 S248 |
2 | BAA09g09060 | A09 | 5042481 | G | A | upstream_gene_variant | MODIFIER | c.-852G>A| |
S175 |
3 | BAA09g09060 | A09 | 5043673 | C | T | missense_variant&splice_region_variant | MODERATE | c.187C>T|p.His63Tyr |
S19 |
4 | BAA09g09060 | A09 | 5043793 | C | T | missense_variant | MODERATE | c.307C>T|p.Leu103Phe |
S183 S198 |
5 | BAA09g09060 | A09 | 5043909 | C | T | missense_variant | MODERATE | c.353C>T|p.Ser118Phe |
S263 |
6 | BAA09g09060 | A09 | 5044019 | C | T | missense_variant | MODERATE | c.463C>T|p.Pro155Ser |
S87 |
7 | BAA09g09060 | A09 | 5044110 | G | A | stop_gained | HIGH | c.554G>A|p.Trp185* |
S88 |
8 | BAA09g09060 | A09 | 5047832 | G | A | downstream_gene_variant | MODIFIER | c.*3011G>A| |
S129 |
9 | BAA09g09060 | A09 | 5049010 | C | T | downstream_gene_variant | MODIFIER | c.*4189C>T| |
S168 |