H38H (p.His38His) variant of CDKN1B (P46527)
H38H (p.His38His) in CDKN1B (P46527) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
H38H (p.His38His) variant details
- p.His38His
- rs141178987
- gnomAD 12-12717953-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.409
- CADD 12.60
- Most common in the 1KG:ASW population (allele frequency 0.0098)
- Structural context available
- Literature evidence available