Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g15500 | A08 | 13069945 | G | A | missense_variant | MODERATE | c.593G>A|p.Gly198Glu |
S192 |
2 | BAA08g15500 | A08 | 13069990 | C | T | missense_variant | MODERATE | c.638C>T|p.Pro213Leu |
S76 |
3 | BAA08g15500 | A08 | 13070073 | C | T | missense_variant | MODERATE | c.721C>T|p.Pro241Ser |
S303 |
4 | BAA08g15500 | A08 | 13070124 | G | A | missense_variant | MODERATE | c.772G>A|p.Glu258Lys |
S159 S187 S188 S243 S276 S298 |
5 | BAA08g15500 | A08 | 13070915 | G | A | missense_variant | MODERATE | c.1405G>A|p.Asp469Asn |
S79 S91 |
6 | BAA08g15500 | A08 | 13070989 | G | A | synonymous_variant | LOW | c.1479G>A|p.Arg493Arg |
S131 |
7 | BAA08g15500 | A08 | 13071016 | C | T | synonymous_variant | LOW | c.1506C>T|p.Ile502Ile |
S60 |
8 | BAA08g15500 | A08 | 13071068 | G | A | missense_variant | MODERATE | c.1558G>A|p.Ala520Thr |
S282 |
9 | BAA08g15500 | A08 | 13071488 | G | A | stop_gained | HIGH | c.1899G>A|p.Trp633* |
S35 |