Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g05210 | A09 | 3012782 | G | A | missense_variant | MODERATE | c.49G>A|p.Asp17Asn |
S75 S81 |
2 | BAA09g05210 | A09 | 3012990 | G | A | missense_variant | MODERATE | c.257G>A|p.Ser86Asn |
S295 |
3 | BAA09g05210 | A09 | 3013421 | G | A | missense_variant | MODERATE | c.688G>A|p.Glu230Lys |
S295 |
4 | BAA09g05210 | A09 | 3013665 | C | T | missense_variant | MODERATE | c.932C>T|p.Thr311Ile |
S249 |
5 | BAA09g05210 | A09 | 3013690 | G | A | synonymous_variant | LOW | c.957G>A|p.Lys319Lys |
S14 |
6 | BAA09g05210 | A09 | 3013841 | G | A | missense_variant | MODERATE | c.1108G>A|p.Glu370Lys |
S124 |
7 | BAA09g05210 | A09 | 3014057 | G | A | missense_variant | MODERATE | c.1324G>A|p.Glu442Lys |
S192 |
8 | BAA09g05210 | A09 | 3014311 | G | A | synonymous_variant | LOW | c.1578G>A|p.Arg526Arg |
S189 |
9 | BAA09g05210 | A09 | 3014819 | G | A | missense_variant | MODERATE | c.1933G>A|p.Glu645Lys |
S201 |
10 | BAA09g05210 | A09 | 3015434 | G | A | missense_variant&splice_region_variant | MODERATE | c.2362G>A|p.Ala788Thr |
S74 |
11 | BAA09g05210 | A09 | 3015692 | G | A | missense_variant | MODERATE | c.2620G>A|p.Ala874Thr |
S255 |