Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26220 | A05 | 30892698 | G | A | synonymous_variant | LOW | c.87G>A|p.Gln29Gln |
S260 |
2 | BAA05g26220 | A05 | 30893508 | G | A | missense_variant&splice_region_variant | MODERATE | c.574G>A|p.Glu192Lys |
S77 |
3 | BAA05g26220 | A05 | 30893671 | G | A | missense_variant | MODERATE | c.654G>A|p.Met218Ile |
S15 S151 S263 |
4 | BAA05g26220 | A05 | 30893675 | C | T | splice_region_variant&synonymous_variant | LOW | c.658C>T|p.Leu220Leu |
S264 |
5 | BAA05g26220 | A05 | 30893996 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.796-1G>A| |
S301 S304 |
6 | BAA05g26220 | A05 | 30894285 | G | A | splice_region_variant&synonymous_variant | LOW | c.993G>A|p.Arg331Arg |
S190 |
7 | BAA05g26220 | A05 | 30895942 | G | A | missense_variant | MODERATE | c.1528G>A|p.Gly510Arg |
S107 |
8 | BAA05g26220 | A05 | 30896638 | G | A | missense_variant | MODERATE | c.1993G>A|p.Gly665Arg |
S82 S92 |
9 | BAA05g26220 | A05 | 30898374 | C | T | synonymous_variant | LOW | c.2671C>T|p.Leu891Leu |
S8 |
10 | BAA05g26220 | A05 | 30898698 | G | A | intron_variant | MODIFIER | c.2779+216G>A| |
S76 |