Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17850 | A05 | 10125120 | C | T | upstream_gene_variant | MODIFIER | c.-2059C>T| |
S256 |
2 | BAA05g17850 | A05 | 10127991 | C | T | missense_variant&splice_region_variant | MODERATE | c.584C>T|p.Ala195Val |
S207 |
3 | BAA05g17850 | A05 | 10128688 | G | A | missense_variant | MODERATE | c.925G>A|p.Asp309Asn |
S244 |
4 | BAA05g17850 | A05 | 10129832 | G | A | downstream_gene_variant | MODIFIER | c.*1043G>A| |
S293 |
5 | BAA05g17850 | A05 | 10130954 | C | T | downstream_gene_variant | MODIFIER | c.*2165C>T| |
S146 |
6 | BAA05g17850 | A05 | 10131073 | G | A | downstream_gene_variant | MODIFIER | c.*2284G>A| |
S306 |
7 | BAA05g17850 | A05 | 10131329 | G | A | downstream_gene_variant | MODIFIER | c.*2540G>A| |
S38 |
8 | BAA05g17850 | A05 | 10131875 | C | T | downstream_gene_variant | MODIFIER | c.*3086C>T| |
S256 |
9 | BAA05g17850 | A05 | 10133427 | G | A | downstream_gene_variant | MODIFIER | c.*4638G>A| |
S62 |
10 | BAA05g17850 | A05 | 10133605 | G | A | downstream_gene_variant | MODIFIER | c.*4816G>A| |
S279 |