Submissions for variant NM_024306.5(FA2H):c.847G>A (p.Val283Ile)

gnomAD frequency: 0.00220  dbSNP: rs138244546

Total submissions: 5

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Illumina Laboratory Services, Illumina	RCV000350126	SCV000398845	benign	Hereditary spastic paraplegia 35	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.
GeneDx	RCV000840125	SCV000982042	likely benign	not provided	2019-07-26	criteria provided, single submitter	clinical testing
Invitae	RCV001085749	SCV001003790	benign	Spastic paraplegia	2024-01-09	criteria provided, single submitter	clinical testing
Athena Diagnostics Inc	RCV000117011	SCV001477236	benign	not specified	2019-12-31	criteria provided, single submitter	clinical testing
Genetic Services Laboratory, University of Chicago	RCV000117011	SCV000151132	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.