T67N (p.Thr67Asn) variant of PRMT5 (O14744)
T67N (p.Thr67Asn) in PRMT5 (O14744) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data, published literature, and structural context.
T67N (p.Thr67Asn) variant details
- p.Thr67Asn
- rs765814196
- gnomAD 14-22920706-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.371
- CADD 14.10
- Most common in the Non-Finnish European population (allele frequency 4.4e-05)
- Structural context available
- Literature evidence available