N34H (p.Asn34His) variant of TCF7L2 (Transcription factor 7-like 2)
N34H (p.Asn34His) in TCF7L2 (Transcription factor 7-like 2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
N34H (p.Asn34His) variant details
- p.Asn34His
- ExAC rs746837026
- TOPMed rs746837026
- gnomAD rs746837026
- Missense
- Variant Prioritization Score for Impact Estimate 0.499
- CADD 23.60
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available