Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05080 | A10 | 2609760 | C | T | upstream_gene_variant | MODIFIER | c.-3381C>T| |
S294 |
2 | BAA10g05080 | A10 | 2610176 | G | A | upstream_gene_variant | MODIFIER | c.-2965G>A| |
S158 |
3 | BAA10g05080 | A10 | 2613243 | C | T | missense_variant | MODERATE | c.103C>T|p.Pro35Ser |
S47 |
4 | BAA10g05080 | A10 | 2613287 | C | T | synonymous_variant | LOW | c.147C>T|p.Tyr49Tyr |
S244 |
5 | BAA10g05080 | A10 | 2613430 | C | T | missense_variant | MODERATE | c.290C>T|p.Ser97Phe |
S15 S156 S2 S3 S34 |
6 | BAA10g05080 | A10 | 2613896 | G | A | missense_variant | MODERATE | c.674G>A|p.Cys225Tyr |
S303 |
7 | BAA10g05080 | A10 | 2614153 | G | A | missense_variant | MODERATE | c.931G>A|p.Gly311Arg |
S125 S164 |
8 | BAA10g05080 | A10 | 2616834 | G | A | downstream_gene_variant | MODIFIER | c.*2577G>A| |
S158 |
9 | BAA10g05080 | A10 | 2616844 | C | T | downstream_gene_variant | MODIFIER | c.*2587C>T| |
S139 |
10 | BAA10g05080 | A10 | 2617363 | C | T | downstream_gene_variant | MODIFIER | c.*3106C>T| |
S203 |