Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05390 | A01 | 2377222 | C | T | synonymous_variant | LOW | c.789C>T|p.Thr263Thr |
S240 |
2 | BAA01g05390 | A01 | 2377816 | G | A | intron_variant | MODIFIER | c.813+570G>A| |
S5 |
3 | BAA01g05390 | A01 | 2378824 | G | A | intron_variant | MODIFIER | c.813+1578G>A| |
S39 |
4 | BAA01g05390 | A01 | 2379894 | G | A | intron_variant | MODIFIER | c.813+2648G>A| |
S6 |
5 | BAA01g05390 | A01 | 2380039 | C | T | intron_variant | MODIFIER | c.813+2793C>T| |
S273 |