V25G (p.Val25Gly) variant of CDKN1A (P38936)
V25G (p.Val25Gly) in CDKN1A (P38936) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data.
V25G (p.Val25Gly) variant details
- p.Val25Gly
- rs765248879
- ClinGen CA3780321
- cosmic curated COSV10584
- ClinVar RCV004141616
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.595
- AlphaMissense 0.77
- MetaLR 0.58
- MetaSVM 0.02
- PolyPhen-2 1.00
- SIFT 0.00
- MutPred 0.73
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available