Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g51480 | A09 | 53804037 | C | T | synonymous_variant | LOW | c.2067G>A|p.Val689Val |
S162 |
2 | BAA09g51480 | A09 | 53804377 | C | T | missense_variant | MODERATE | c.1727G>A|p.Arg576Gln |
S208 |
3 | BAA09g51480 | A09 | 53805131 | G | A | missense_variant | MODERATE | c.1181C>T|p.Ser394Phe |
S135 |
4 | BAA09g51480 | A09 | 53805161 | C | T | missense_variant | MODERATE | c.1151G>A|p.Arg384Lys |
S37 |
5 | BAA09g51480 | A09 | 53807082 | G | A | missense_variant&splice_region_variant | MODERATE | c.278C>T|p.Pro93Leu |
S128 |
6 | BAA09g51480 | A09 | 53809305 | C | T | upstream_gene_variant | MODIFIER | c.-1946G>A| |
S293 |
7 | BAA09g51480 | A09 | 53809880 | G | A | upstream_gene_variant | MODIFIER | c.-2521C>T| |
S247 |
8 | BAA09g51480 | A09 | 53812201 | G | A | upstream_gene_variant | MODIFIER | c.-4842C>T| |
S178 |