S49F (p.Ser49Phe) variant of TTN (Titin)
S49F (p.Ser49Phe) in TTN (Titin) is a missense change. The record also includes variant effect predictions and population frequency data.
S49F (p.Ser49Phe) variant details
- p.Ser49Phe
- ESP rs368887734
- ExAC rs368887734
- TOPMed rs368887734
- gnomAD rs368887734
- Missense
- CADD 27.50
- Population evidence available