G68D (p.Gly68Asp) variant of BMPR2 (Q13873)
G68D (p.Gly68Asp) in BMPR2 (Q13873) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as pathogenic in the context of Pulmonary hypertension, primary, 1; Pulmonary arterial hypertension. The available variant effect predictions contribute to a CATVariant prioritization score of 0.94 / 1. The record also includes published literature and structural context.
G68D (p.Gly68Asp) variant details
- p.Gly68Asp
- rs1085307180
- ClinGen CA350399390
- cosmic curated COSV65809
- ClinVar RCV000488700
- Pathogenic
- Pulmonary hypertension, primary, 1; Pulmonary arterial hypertension
- Missense
- Variant Prioritization Score for Impact Estimate 0.941
- AlphaMissense 1.00
- MetaLR 0.96
- MetaSVM 1.09
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.86
- ClinVar: Pathogenic (Pulmonary hypertension, primary, 1; Pulmonary arterial hypertens)
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available
- Cited in: Heritable Pulmonary Arterial Hypertension Overview. (PMID 20301658)