Submissions for variant NM_000494.4(COL17A1):c.629C>T (p.Thr210Met)

gnomAD frequency: 0.59454  dbSNP: rs805708

Total submissions: 7

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
PreventionGenetics, part of Exact Sciences	RCV000252360	SCV000304525	benign	not specified		criteria provided, single submitter	clinical testing
Illumina Laboratory Services, Illumina	RCV000264886	SCV000360277	benign	Junctional epidermolysis bullosa, non-Herlitz type	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 benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.
Genome-Nilou Lab	RCV000264886	SCV001821788	benign	Junctional epidermolysis bullosa, non-Herlitz type	2021-07-22	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV001589241	SCV001821789	benign	Epithelial recurrent erosion dystrophy	2021-07-22	criteria provided, single submitter	clinical testing
GeneDx	RCV001711656	SCV001946062	benign	not provided	2015-03-03	criteria provided, single submitter	clinical testing
Labcorp Genetics (formerly Invitae), Labcorp	RCV001711656	SCV002407824	benign	not provided	2024-02-01	criteria provided, single submitter	clinical testing
Breakthrough Genomics, Breakthrough Genomics	RCV001711656	SCV005317126	benign	not provided		criteria provided, single submitter	not provided