Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18440 | A02 | 9407770 | A | C | missense_variant | MODERATE | c.622T>G|p.Ser208Ala |
S5 |
2 | BAA02g18440 | A02 | 9407780 | G | A | synonymous_variant | LOW | c.612C>T|p.Cys204Cys |
S5 |
3 | BAA02g18440 | A02 | 9407789 | G | A | synonymous_variant | LOW | c.603C>T|p.Asp201Asp |
S5 |
4 | BAA02g18440 | A02 | 9407803 | C | T | missense_variant | MODERATE | c.589G>A|p.Val197Ile |
S5 |
5 | BAA02g18440 | A02 | 9407807 | A | T | missense_variant | MODERATE | c.585T>A|p.His195Gln |
S5 |
6 | BAA02g18440 | A02 | 9407887 | C | T | missense_variant | MODERATE | c.505G>A|p.Ala169Thr |
S163 |
7 | BAA02g18440 | A02 | 9408092 | G | A | synonymous_variant | LOW | c.300C>T|p.Asp100Asp |
S136 |
8 | BAA02g18440 | A02 | 9408268 | C | T | missense_variant | MODERATE | c.124G>A|p.Asp42Asn |
S242 |