Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26770 | A09 | 17417002 | G | A | stop_gained | HIGH | c.319C>T|p.Gln107* |
S221 |
2 | BAA09g26770 | A09 | 17417059 | G | A | missense_variant | MODERATE | c.262C>T|p.Pro88Ser |
S259 |
3 | BAA09g26770 | A09 | 17417561 | G | A | synonymous_variant | LOW | c.171C>T|p.Leu57Leu |
S271 |
4 | BAA09g26770 | A09 | 17418860 | G | A | upstream_gene_variant | MODIFIER | c.-956C>T| |
S80 |
5 | BAA09g26770 | A09 | 17419538 | C | T | upstream_gene_variant | MODIFIER | c.-1634G>A| |
S54 |
6 | BAA09g26770 | A09 | 17421607 | C | T | upstream_gene_variant | MODIFIER | c.-3703G>A| |
S161 |
7 | BAA09g26770 | A09 | 17421812 | C | T | upstream_gene_variant | MODIFIER | c.-3908G>A| |
S153 |