Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17110 | A10 | 16622711 | C | T | missense_variant | MODERATE | c.2263G>A|p.Asp755Asn |
S302 |
2 | BAA10g17110 | A10 | 16626629 | C | T | upstream_gene_variant | MODIFIER | c.-1656G>A| |
S168 |
3 | BAA10g17110 | A10 | 16628137 | C | T | upstream_gene_variant | MODIFIER | c.-3164G>A| |
S10 |
4 | BAA10g17110 | A10 | 16628750 | G | A | upstream_gene_variant | MODIFIER | c.-3777C>T| |
S234 |
5 | BAA10g17110 | A10 | 16628891 | C | T | upstream_gene_variant | MODIFIER | c.-3918G>A| |
S25 |
6 | BAA10g17110 | A10 | 16628916 | C | T | upstream_gene_variant | MODIFIER | c.-3943G>A| |
S271 |
7 | BAA10g17110 | A10 | 16629305 | G | A | upstream_gene_variant | MODIFIER | c.-4332C>T| |
S57 |