A13S (p.Ala13Ser) variant of BCR (P11274)
A13S (p.Ala13Ser) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
A13S (p.Ala13Ser) variant details
- p.Ala13Ser
- Ensembl rs2146187440
- Missense
- Variant Prioritization Score for Impact Estimate 0.474
- REVEL 0.30
- CADD 26.30
- PolyPhen-2 0.99
- SIFT 0.01
- Most common in the HGDP:FRENCH population (allele frequency 0.019)
- Structural context available