Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g36930 | A09 | 45115086 | C | T | missense_variant | MODERATE | c.838G>A|p.Gly280Arg |
S165 |
2 | BAA09g36930 | A09 | 45116661 | C | T | synonymous_variant | LOW | c.6G>A|p.Ala2Ala |
S229 |
3 | BAA09g36930 | A09 | 45118016 | A | T | upstream_gene_variant | MODIFIER | c.-1350T>A| |
S234 |
4 | BAA09g36930 | A09 | 45118427 | C | T | upstream_gene_variant | MODIFIER | c.-1761G>A| |
S63 |
5 | BAA09g36930 | A09 | 45118543 | G | A | upstream_gene_variant | MODIFIER | c.-1877C>T| |
S73 S91 |
6 | BAA09g36930 | A09 | 45120415 | C | T | upstream_gene_variant | MODIFIER | c.-3749G>A| |
S33 |