F7L (p.Phe7Leu) variant of BCR (P11274)
F7L (p.Phe7Leu) in BCR (P11274) 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 0.50 / 1. The record also includes population frequency data and structural context.
F7L (p.Phe7Leu) variant details
- p.Phe7Leu
- rs1233802398
- NCI-TCGA Cosmic COSV1000
- cosmic curated COSV10000
- gnomAD rs1233802398
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.501
- REVEL 0.42
- CADD 28.70
- PolyPhen-2 0.97
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available