Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46080 | A09 | 51018033 | C | T | missense_variant | MODERATE | c.1181G>A|p.Gly394Asp |
S94 |
2 | BAA09g46080 | A09 | 51018168 | G | A | missense_variant | MODERATE | c.1046C>T|p.Ala349Val |
S193 |
3 | BAA09g46080 | A09 | 51018654 | G | A | missense_variant | MODERATE | c.560C>T|p.Ser187Leu |
S268 |
4 | BAA09g46080 | A09 | 51018900 | G | A | missense_variant | MODERATE | c.314C>T|p.Ser105Phe |
S246 |
5 | BAA09g46080 | A09 | 51018938 | C | T | synonymous_variant | LOW | c.276G>A|p.Arg92Arg |
S96 |
6 | BAA09g46080 | A09 | 51019195 | C | T | missense_variant | MODERATE | c.19G>A|p.Asp7Asn |
S295 |
7 | BAA09g46080 | A09 | 51019746 | G | A | upstream_gene_variant | MODIFIER | c.-533C>T| |
S156 |
8 | BAA09g46080 | A09 | 51020053 | C | T | upstream_gene_variant | MODIFIER | c.-840G>A| |
S297 |
9 | BAA09g46080 | A09 | 51020110 | G | A | upstream_gene_variant | MODIFIER | c.-897C>T| |
S57 |
10 | BAA09g46080 | A09 | 51022766 | G | A | upstream_gene_variant | MODIFIER | c.-3553C>T| |
S244 |
11 | BAA09g46080 | A09 | 51023028 | C | T | upstream_gene_variant | MODIFIER | c.-3815G>A| |
S223 |
12 | BAA09g46080 | A09 | 51023187 | C | T | upstream_gene_variant | MODIFIER | c.-3974G>A| |
S204 |