Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64960 | A09 | 60064405 | G | A | synonymous_variant | LOW | c.1114C>T|p.Leu372Leu |
S69 |
2 | BAA09g64960 | A09 | 60064587 | G | A | missense_variant | MODERATE | c.932C>T|p.Ser311Phe |
S74 |
3 | BAA09g64960 | A09 | 60065091 | G | A | missense_variant | MODERATE | c.505C>T|p.Pro169Ser |
S39 |
4 | BAA09g64960 | A09 | 60065796 | G | A | splice_region_variant&intron_variant | LOW | c.15+7C>T| |
S275 |
5 | BAA09g64960 | A09 | 60065890 | C | T | upstream_gene_variant | MODIFIER | c.-73G>A| |
S100 |
6 | BAA09g64960 | A09 | 60066498 | T | A | upstream_gene_variant | MODIFIER | c.-681A>T| |
S54 |