Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g14160 | A01 | 6721173 | G | A | missense_variant | MODERATE | c.55G>A|p.Glu19Lys |
S121 |
2 | BAA01g14160 | A01 | 6721274 | C | T | synonymous_variant | LOW | c.156C>T|p.Arg52Arg |
S77 |
3 | BAA01g14160 | A01 | 6721454 | G | A | synonymous_variant | LOW | c.336G>A|p.Glu112Glu |
S288 |
4 | BAA01g14160 | A01 | 6721796 | C | T | synonymous_variant | LOW | c.678C>T|p.His226His |
S303 |
5 | BAA01g14160 | A01 | 6721972 | G | A | missense_variant | MODERATE | c.854G>A|p.Ser285Asn |
S187 |
6 | BAA01g14160 | A01 | 6722008 | G | A | missense_variant | MODERATE | c.890G>A|p.Arg297Lys |
S280 |
7 | BAA01g14160 | A01 | 6722634 | G | A | missense_variant | MODERATE | c.1516G>A|p.Glu506Lys |
S202 |
8 | BAA01g14160 | A01 | 6722748 | C | T | missense_variant | MODERATE | c.1630C>T|p.Pro544Ser |
S5 |
9 | BAA01g14160 | A01 | 6722819 | G | A | synonymous_variant | LOW | c.1701G>A|p.Lys567Lys |
S212 |
10 | BAA01g14160 | A01 | 6722855 | C | T | synonymous_variant | LOW | c.1737C>T|p.Arg579Arg |
S189 |