P35A (p.Pro35Ala) variant of CDKN1B (P46527)
P35A (p.Pro35Ala) in CDKN1B (P46527) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Multiple endocrine neoplasia type 4. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes published literature and structural context.
P35A (p.Pro35Ala) variant details
- p.Pro35Ala
- rs1946488503
- ClinGen CA383968611
- ClinVar RCV001327314
- Ensembl rs1946488503
- Uncertain significance
- Multiple endocrine neoplasia type 4
- Missense
- Variant Prioritization Score for Impact Estimate 0.588
- AlphaMissense 0.19
- MetaLR 0.75
- MetaSVM 0.52
- PolyPhen-2 0.71
- SIFT 0.11
- EVE 0.29
- ClinVar: Uncertain significance (Multiple endocrine neoplasia type 4)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Cancer Genetics Risk Assessment and Counseling (PDQ®): Health Professional Version. (PMID 26389258)
- Cited in: Genetics of Endocrine and Neuroendocrine Neoplasias (PDQ®): Health Professional Version. (PMID 26389271)