I67F (p.Ile67Phe) variant of SRD5A2 (P31213)
I67F (p.Ile67Phe) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
I67F (p.Ile67Phe) variant details
- p.Ile67Phe
- ESP rs371573955
- ExAC rs371573955
- TOPMed rs371573955
- gnomAD rs371573955
- Missense
- Variant Prioritization Score for Impact Estimate 0.29
- CADD 14.20
- PolyPhen-2 0.03
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available