N51N (p.Asn51Asn) variant of HSD3B2 (P26439)
N51N (p.Asn51Asn) in HSD3B2 (P26439) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
N51N (p.Asn51Asn) variant details
- p.Asn51Asn
- gnomAD 1-119419428-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.148
- CADD 1.04
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available