A13T (p.Ala13Thr) variant of BCR (P11274)
A13T (p.Ala13Thr) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data, published literature, and structural context.
A13T (p.Ala13Thr) variant details
- p.Ala13Thr
- gnomAD 22-23180997-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.497
- REVEL 0.33
- CADD 27.70
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available
- Literature evidence available