D42G (p.Asp42Gly) variant of TTN (Titin)
D42G (p.Asp42Gly) in TTN (Titin) is a missense change. The record also includes variant effect predictions and population frequency data.
D42G (p.Asp42Gly) variant details
- p.Asp42Gly
- TOPMed rs200838218
- gnomAD rs200838218
- Missense
- CADD 29.80
- PolyPhen-2 1.00
- Population evidence available