V6G (p.Val6Gly) variant of CDKN1B (P46527)
V6G (p.Val6Gly) in CDKN1B (P46527) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data, published literature, and structural context.
V6G (p.Val6Gly) variant details
- p.Val6Gly
- gnomAD 12-12717856-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.664
- REVEL 0.67
- CADD 29.30
- PolyPhen-2 0.71
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available