Submissions for variant NM_182925.5(FLT4):c.1921C>T (p.Pro641Ser)

gnomAD frequency: 0.00349  dbSNP: rs55667289

Total submissions: 10

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
PreventionGenetics, part of Exact Sciences	RCV000245029	SCV000316791	likely benign	not specified		criteria provided, single submitter	clinical testing
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics	RCV000428505	SCV000510616	likely benign	not provided	2016-07-13	criteria provided, single submitter	clinical testing	Converted during submission to Likely benign.
Invitae	RCV000428505	SCV001001600	benign	not provided	2019-12-31	criteria provided, single submitter	clinical testing
Mendelics	RCV000987648	SCV001137046	likely benign	Carcinoma of colon	2019-05-28	criteria provided, single submitter	clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	RCV000428505	SCV002048008	likely benign	not provided	2023-10-26	criteria provided, single submitter	clinical testing
CeGaT Center for Human Genetics Tuebingen	RCV000428505	SCV004032654	likely benign	not provided	2024-01-01	criteria provided, single submitter	clinical testing	FLT4: BS1
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV000428505	SCV001743383	likely benign	not provided		no assertion criteria provided	clinical testing
Clinical Genetics, Academic Medical Center	RCV000428505	SCV001916980	likely benign	not provided		no assertion criteria provided	clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+	RCV000245029	SCV001955293	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center	RCV000428505	SCV001976196	likely benign	not provided		no assertion criteria provided	clinical testing