D68N (p.Asp68Asn) variant of WWTR1 (Q9GZV5)
D68N (p.Asp68Asn) in WWTR1 (Q9GZV5) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
D68N (p.Asp68Asn) variant details
- p.Asp68Asn
- cosmic curated COSV10525
- Missense
- Variant Prioritization Score for Impact Estimate 0.439
- REVEL 0.16
- CADD 31.00
- PolyPhen-2 0.98
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available