G10W (p.Gly10Trp) variant of CNTNAP2 (Q9UHC6)
G10W (p.Gly10Trp) in CNTNAP2 (Q9UHC6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
G10W (p.Gly10Trp) variant details
- p.Gly10Trp
- gnomAD rs1169898267
- Missense
- Variant Prioritization Score for Impact Estimate 0.448
- REVEL 0.38
- CADD 23.40
- PolyPhen-2 0.34
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.9e-06)
- Structural context available