N66N (p.Asn66Asn) variant of NOS1AP (O75052)
N66N (p.Asn66Asn) in NOS1AP (O75052) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data, published literature, and structural context.
N66N (p.Asn66Asn) variant details
- p.Asn66Asn
- gnomAD 1-162287364-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.211
- CADD 7.01
- Most common in the Non-Finnish European population (allele frequency 9e-06)
- Structural context available
- Literature evidence available