Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.24357700C>T | CA136643275 | DCDC2,KAAG1 | c.61C>T (p.Leu21Phe) c.51G>A (p.Lys17=) n.798C>T | dbSNP gnomAD v3 gnomAD v4 |
6 | g.24357700C>G | CA16616872 | DCDC2,KAAG1 | c.61C>G (p.Leu21Val) c.51G>C (p.Lys17Asn) n.798C>G | ClinVar dbSNP |