Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g42090 | A09 | 48617107 | G | A | missense_variant | MODERATE | c.211C>T|p.His71Tyr |
S262 |
2 | BAA09g42090 | A09 | 48620117 | C | T | upstream_gene_variant | MODIFIER | c.-1123G>A| |
S183 |
3 | BAA09g42090 | A09 | 48622067 | G | A | upstream_gene_variant | MODIFIER | c.-3073C>T| |
S15 S3 |
4 | BAA09g42090 | A09 | 48623271 | G | A | upstream_gene_variant | MODIFIER | c.-4277C>T| |
S252 |
5 | BAA09g42090 | A09 | 48623929 | G | A | upstream_gene_variant | MODIFIER | c.-4935C>T| |
S181 |