Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39460 | A09 | 47069015 | G | A | missense_variant | MODERATE | c.1240C>T|p.Pro414Ser |
S298 |
2 | BAA09g39460 | A09 | 47069079 | C | T | missense_variant | MODERATE | c.1176G>A|p.Met392Ile |
S279 |
3 | BAA09g39460 | A09 | 47069289 | C | T | synonymous_variant | LOW | c.966G>A|p.Gln322Gln |
S136 |
4 | BAA09g39460 | A09 | 47069717 | G | A | missense_variant | MODERATE | c.538C>T|p.His180Tyr |
S172 S217 |
5 | BAA09g39460 | A09 | 47070839 | C | T | upstream_gene_variant | MODIFIER | c.-585G>A| |
S296 |
6 | BAA09g39460 | A09 | 47070859 | C | T | upstream_gene_variant | MODIFIER | c.-605G>A| |
S30 S31 |
7 | BAA09g39460 | A09 | 47072253 | C | T | upstream_gene_variant | MODIFIER | c.-1999G>A| |
S293 |
8 | BAA09g39460 | A09 | 47074974 | C | T | upstream_gene_variant | MODIFIER | c.-4720G>A| |
S80 |