Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g04980 | A01 | 2198388 | G | A | upstream_gene_variant | MODIFIER | c.-1906G>A| |
S54 |
2 | BAA01g04980 | A01 | 2198856 | G | A | upstream_gene_variant | MODIFIER | c.-1438G>A| |
S8 |
3 | BAA01g04980 | A01 | 2199309 | C | T | upstream_gene_variant | MODIFIER | c.-985C>T| |
S8 |
4 | BAA01g04980 | A01 | 2199847 | C | T | upstream_gene_variant | MODIFIER | c.-447C>T| |
S64 |
5 | BAA01g04980 | A01 | 2200153 | C | T | upstream_gene_variant | MODIFIER | c.-141C>T| |
S111 |
6 | BAA01g04980 | A01 | 2200332 | G | A | synonymous_variant | LOW | c.39G>A|p.Lys13Lys |
S295 |
7 | BAA01g04980 | A01 | 2200440 | T | A | synonymous_variant | LOW | c.147T>A|p.Leu49Leu |
S269 |
8 | BAA01g04980 | A01 | 2200644 | C | T | missense_variant | MODERATE | c.256C>T|p.His86Tyr |
S48 |
9 | BAA01g04980 | A01 | 2200869 | C | T | stop_gained | HIGH | c.481C>T|p.Gln161* |
S129 |