F92L (p.Phe92Leu) variant of CALCRL (Q16602)
F92L (p.Phe92Leu) in CALCRL (Q16602) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
F92L (p.Phe92Leu) variant details
- p.Phe92Leu
- NCI-TCGA Cosmic COSV6647
- cosmic curated COSV66475
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.546
- REVEL 0.48
- CADD 26.40
- PolyPhen-2 0.50
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available