F5L (p.Phe5Leu) variant of ABCC2 (Q92887)
F5L (p.Phe5Leu) in ABCC2 (Q92887) 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 0.60 / 1. The record also includes population frequency data and structural context.
F5L (p.Phe5Leu) variant details
- p.Phe5Leu
- NCI-TCGA Cosmic COSV6497
- cosmic curated COSV64971
- Ensembl rs2037638876
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.596
- CADD 23.00
- PolyPhen-2 0.13
- SIFT 0.17
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available