T62N (p.Thr62Asn) variant of RAMP1 (O60894)
T62N (p.Thr62Asn) in RAMP1 (O60894) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data, published literature, and structural context.
T62N (p.Thr62Asn) variant details
- p.Thr62Asn
- gnomAD 2-237877356-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.5
- REVEL 0.31
- CADD 23.50
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available