P14S (p.Pro14Ser) variant of CALCRL (Q16602)
P14S (p.Pro14Ser) in CALCRL (Q16602) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
P14S (p.Pro14Ser) variant details
- p.Pro14Ser
- TOPMed rs1464838331
- gnomAD rs1464838331
- Missense
- Variant Prioritization Score for Impact Estimate 0.116
- REVEL 0.09
- CADD 0.78
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available