Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g15590 | A09 | 8937634 | C | T | upstream_gene_variant | MODIFIER | c.-4412C>T| |
S114 |
2 | BAA09g15590 | A09 | 8937852 | G | A | upstream_gene_variant | MODIFIER | c.-4194G>A| |
S151 |
3 | BAA09g15590 | A09 | 8941213 | C | T | upstream_gene_variant | MODIFIER | c.-833C>T| |
S293 |
4 | BAA09g15590 | A09 | 8942314 | G | A | missense_variant | MODERATE | c.269G>A|p.Arg90Lys |
S192 |
5 | BAA09g15590 | A09 | 8942462 | G | A | synonymous_variant | LOW | c.417G>A|p.Thr139Thr |
S16 S160 |
6 | BAA09g15590 | A09 | 8942513 | C | T | synonymous_variant | LOW | c.468C>T|p.Ile156Ile |
S174 S27 |
7 | BAA09g15590 | A09 | 8942615 | G | A | synonymous_variant | LOW | c.570G>A|p.Gln190Gln |
S142 |
8 | BAA09g15590 | A09 | 8944693 | C | T | downstream_gene_variant | MODIFIER | c.*1949C>T| |
S211 |
9 | BAA09g15590 | A09 | 8945396 | C | T | downstream_gene_variant | MODIFIER | c.*2652C>T| |
S200 |
10 | BAA09g15590 | A09 | 8945945 | C | T | downstream_gene_variant | MODIFIER | c.*3201C>T| |
S295 |