Submissions for variant NM_002291.3(LAMB1):c.979C>T (p.Arg327Ter)

Total submissions: 1

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Neuberg Centre For Genomic Medicine, NCGM	RCV004577220	SCV005061135	likely pathogenic	Cobblestone lissencephaly without muscular or ocular involvement		criteria provided, single submitter	clinical testing	The observed stop gained c.979C>T (p.Arg327Ter) variant in LAMB1 gene has not been previously reported as a pathogenic variant nor as a benign variant, to our knowledge. The p.Arg327Ter variant has been reported with allele frequency of 0.004% in gnomAD Exomes. This variant has not been submitted to the ClinVar database. The nucleotide change c.979C>T in LAMB1 is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. This sequence change creates a premature translational stop signal (p.Arg327Ter) in the LAMB1 gene. This variant is predicted to cause loss of normal protein function through protein truncation. Loss of function variants in LAMB1 gene have been previously reported to be pathogenic (Radmanesh et al., 2013). Computational evidence (MutationTaster - Disease causing) predicts damaging effect on protein structure and function for this variant. However, additional functional studies will be required to prove the pathogenicity of this variant. For these reasons, this variant has been classified as Likely Pathogenic.