L41F (p.Leu41Phe) variant of CALCB (P10092)
L41F (p.Leu41Phe) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
L41F (p.Leu41Phe) variant details
- p.Leu41Phe
- cosmic curated COSV10015
- Ensembl rs1850381939
- Missense
- Variant Prioritization Score for Impact Estimate 0.211
- REVEL 0.09
- CADD 16.40
- PolyPhen-2 0.02
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available