Submissions for variant NM_198525.3(KIF7):c.3013G>A (p.Gly1005Arg)

gnomAD frequency: 0.52523  dbSNP: rs12900805

Total submissions: 14

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Eurofins Ntd Llc (ga)	RCV000082815	SCV000114863	benign	not specified	2014-11-14	criteria provided, single submitter	clinical testing
PreventionGenetics, part of Exact Sciences	RCV000082815	SCV000316985	benign	not specified		criteria provided, single submitter	clinical testing
Illumina Laboratory Services, Illumina	RCV000332349	SCV000394325	benign	Acrocallosal syndrome	2018-01-13	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.
Invitae	RCV000332349	SCV001731355	benign	Acrocallosal syndrome	2024-01-31	criteria provided, single submitter	clinical testing
GeneDx	RCV001682792	SCV001897862	benign	not provided	2015-03-03	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV001730517	SCV001981088	benign	Multiple epiphyseal dysplasia, Al-Gazali type	2021-08-19	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV001730518	SCV001981089	benign	Hydrolethalus syndrome 2	2021-08-19	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV000332349	SCV001981091	benign	Acrocallosal syndrome	2021-08-19	criteria provided, single submitter	clinical testing
Genetic Services Laboratory, University of Chicago	RCV000082815	SCV000151621	likely benign	not specified		no assertion criteria provided	clinical testing	Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated disease phenotype. NOT Sanger confirmed.
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV000082815	SCV001741510	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics, Academic Medical Center	RCV000082815	SCV001925412	benign	not specified		no assertion criteria provided	clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht	RCV000082815	SCV001927468	benign	not specified		no assertion criteria provided	clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+	RCV000082815	SCV001959963	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center	RCV000082815	SCV001969609	benign	not specified		no assertion criteria provided	clinical testing