N102D (p.Asn102Asp) variant of SRD5A2 (P31213)
N102D (p.Asn102Asp) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data and structural context.
N102D (p.Asn102Asp) variant details
- p.Asn102Asp
- gnomAD rs1477387133
- Missense
- Variant Prioritization Score for Impact Estimate 0.585
- CADD 22.10
- PolyPhen-2 0.04
- SIFT 0.15
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available