Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44000 | A09 | 49891426 | C | T | missense_variant | MODERATE | c.710G>A|p.Ser237Asn |
S92 |
2 | BAA09g44000 | A09 | 49891971 | G | A | synonymous_variant | LOW | c.240C>T|p.Phe80Phe |
S150 |
3 | BAA09g44000 | A09 | 49892174 | G | A | stop_gained | HIGH | c.37C>T|p.Gln13* |
S271 |
4 | BAA09g44000 | A09 | 49892194 | G | A | missense_variant | MODERATE | c.17C>T|p.Ser6Phe |
S246 |
5 | BAA09g44000 | A09 | 49892201 | C | T | missense_variant | MODERATE | c.10G>A|p.Gly4Arg |
S152 |
6 | BAA09g44000 | A09 | 49893524 | C | T | upstream_gene_variant | MODIFIER | c.-1314G>A| |
S183 S198 |
7 | BAA09g44000 | A09 | 49893983 | G | A | upstream_gene_variant | MODIFIER | c.-1773C>T| |
S177 |
8 | BAA09g44000 | A09 | 49893998 | C | T | upstream_gene_variant | MODIFIER | c.-1788G>A| |
S55 |
9 | BAA09g44000 | A09 | 49894119 | C | T | upstream_gene_variant | MODIFIER | c.-1909G>A| |
S181 |
10 | BAA09g44000 | A09 | 49894798 | C | T | upstream_gene_variant | MODIFIER | c.-2588G>A| |
S35 |
11 | BAA09g44000 | A09 | 49895054 | C | T | upstream_gene_variant | MODIFIER | c.-2844G>A| |
S168 |
12 | BAA09g44000 | A09 | 49896018 | A | T | upstream_gene_variant | MODIFIER | c.-3808T>A| |
S76 |
13 | BAA09g44000 | A09 | 49896100 | C | T | upstream_gene_variant | MODIFIER | c.-3890G>A| |
S118 |
14 | BAA09g44000 | A09 | 49896227 | G | A | upstream_gene_variant | MODIFIER | c.-4017C>T| |
S266 |