D13N (p.Asp13Asn) variant of MAPT (P10636)
D13N (p.Asp13Asn) in MAPT (P10636) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
D13N (p.Asp13Asn) variant details
- p.Asp13Asn
- rs773820376
- NCI-TCGA Cosmic COSV5223
- cosmic curated COSV52238
- ExAC rs773820376
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.401
- AlphaMissense 0.20
- MetaLR 0.21
- MetaSVM -0.76
- PolyPhen-2 1.00
- SIFT 0.00
- MutPred 0.22
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available