P16T (p.Pro16Thr) variant of BCR (P11274)
P16T (p.Pro16Thr) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
P16T (p.Pro16Thr) variant details
- p.Pro16Thr
- 1000Genomes rs2072242440
- gnomAD rs2072242440
- Missense
- Variant Prioritization Score for Impact Estimate 0.347
- REVEL 0.11
- CADD 22.90
- PolyPhen-2 0.38
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 0.00041)
- Structural context available