ClinVar (all) for Orgtrack (Select 507708) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 977217	NM_000228.3(LAMB3):c.2188C>T (p.Gln730Ter)	LAMB3 (Q730*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 370778	NM_000228.3(LAMB3):c.3119G>A (p.Trp1040Ter)	LAMB3 (W1040*)	Single nucleotide variant (nonsense)	not provided +2 more	GPathogenic/Likely pathogenic