Submissions for variant NM_033100.4(CDHR1):c.1071C>T (p.Ser357=)

gnomAD frequency: 0.00167  dbSNP: rs146588811

Total submissions: 5

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Illumina Laboratory Services, Illumina	RCV000625430	SCV000365421	uncertain significance	Cone-rod dystrophy 15	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, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.
CeGaT Center for Human Genetics Tuebingen	RCV000415766	SCV000493295	uncertain significance	not provided	2016-08-01	criteria provided, single submitter	clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center	RCV000625430	SCV000745342	likely benign	Cone-rod dystrophy 15	2017-06-28	criteria provided, single submitter	clinical testing
Invitae	RCV000415766	SCV001107229	likely benign	not provided	2024-01-25	criteria provided, single submitter	clinical testing
Clinical Genetics, Academic Medical Center	RCV001699435	SCV001922013	benign	not specified		no assertion criteria provided	clinical testing