Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19730 | A10 | 18006328 | G | A | missense_variant | MODERATE | c.214G>A|p.Glu72Lys |
S240 |
2 | BAA10g19730 | A10 | 18007870 | C | T | synonymous_variant | LOW | c.1248C>T|p.Arg416Arg |
S10 |
3 | BAA10g19730 | A10 | 18008700 | C | T | missense_variant | MODERATE | c.1715C>T|p.Thr572Ile |
S200 |
4 | BAA10g19730 | A10 | 18009195 | G | A | missense_variant | MODERATE | c.2030G>A|p.Gly677Glu |
S143 |
5 | BAA10g19730 | A10 | 18009220 | C | T | splice_region_variant&synonymous_variant | LOW | c.2055C>T|p.Phe685Phe |
S2 |
6 | BAA10g19730 | A10 | 18010060 | C | T | splice_region_variant&synonymous_variant | LOW | c.2484C>T|p.Val828Val |
S246 |