G128W (p.Gly128Trp) variant of CDKN1C (P49918)
G128W (p.Gly128Trp) in CDKN1C (P49918) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data, published literature, and structural context.
G128W (p.Gly128Trp) variant details
- p.Gly128Trp
- gnomAD 11-2883845-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.444
- CADD 20.40
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available
- Literature evidence available