Submissions for variant NM_006031.6(PCNT):c.6634C>T (p.Arg2212Trp)

gnomAD frequency: 0.00516  dbSNP: rs144471022

Total submissions: 8

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Genetic Services Laboratory, University of Chicago	RCV000177472	SCV000194540	likely benign	not specified	2015-07-29	criteria provided, single submitter	clinical testing
Eurofins Ntd Llc (ga)	RCV000177472	SCV000229333	benign	not specified	2015-04-22	criteria provided, single submitter	clinical testing
Illumina Laboratory Services, Illumina	RCV000378936	SCV000437051	likely benign	Microcephalic osteodysplastic primordial dwarfism type II	2018-01-12	criteria provided, single submitter	clinical testing	This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as likely benign is not then subjected to further curation. The score for this variant resulted in a classification of likely benign for this disease.
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics	RCV000513840	SCV000610192	likely benign	not provided	2017-09-05	criteria provided, single submitter	clinical testing
GeneDx	RCV000177472	SCV000729415	benign	not specified	2018-02-20	criteria provided, single submitter	clinical testing	This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae	RCV000513840	SCV001101729	benign	not provided	2024-01-31	criteria provided, single submitter	clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	RCV000378936	SCV001471236	benign	Microcephalic osteodysplastic primordial dwarfism type II	2020-12-05	criteria provided, single submitter	clinical testing
CeGaT Center for Human Genetics Tuebingen	RCV000513840	SCV004152034	likely benign	not provided	2023-12-01	criteria provided, single submitter	clinical testing	PCNT: BP4, BS2