V8M (p.Val8Met) variant of CDKN1A (P38936)
V8M (p.Val8Met) in CDKN1A (P38936) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and published literature.
V8M (p.Val8Met) variant details
- p.Val8Met
- gnomAD 22-46248251-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.154
- REVEL 0.00
- MetaLR 0.04
- MetaSVM -1.04
- CADD 10.10
- PolyPhen-2 0.01
- SIFT 0.34
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Literature evidence available