S68N (p.Ser68Asn) variant of MAPT (P10636)
S68N (p.Ser68Asn) in MAPT (P10636) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
S68N (p.Ser68Asn) variant details
- p.Ser68Asn
- TOPMed rs1447868249
- gnomAD rs1447868249
- Missense
- Variant Prioritization Score for Impact Estimate 0.364
- REVEL 0.19
- MetaLR 0.19
- MetaSVM -0.89
- CADD 25.70
- PolyPhen-2 0.17
- SIFT 0.03
- Population evidence available
- Structural context available