D13N (p.Asp13Asn) variant of GNA11 (P29992)
D13N (p.Asp13Asn) in GNA11 (P29992) 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, published literature, and structural context.
D13N (p.Asp13Asn) variant details
- p.Asp13Asn
- gnomAD 19-3094688-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.445
- REVEL 0.30
- CADD 23.50
- PolyPhen-2 0.07
- SIFT 0.21
- Population evidence available
- Structural context available
- Literature evidence available