P89S (p.Pro89Ser) variant of CALCRL (Q16602)
P89S (p.Pro89Ser) in CALCRL (Q16602) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data and structural context.
P89S (p.Pro89Ser) variant details
- p.Pro89Ser
- ExAC rs759762165
- gnomAD rs759762165
- Missense
- Variant Prioritization Score for Impact Estimate 0.775
- REVEL 0.77
- CADD 26.60
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available