T38N (p.Thr38Asn) variant of ETFDH (Q16134)
T38N (p.Thr38Asn) in ETFDH (Q16134) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
T38N (p.Thr38Asn) variant details
- p.Thr38Asn
- TOPMed rs1773826904
- Missense
- Variant Prioritization Score for Impact Estimate 0.211
- REVEL 0.32
- CADD 0.01
- PolyPhen-2 0.00
- SIFT 0.42
- Population evidence available
- Structural context available