"SIB Swiss Institute of Bioinformatics"[submitter] AND "CALM1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 39757	NM_006888.6(CALM1):c.161A>T (p.Asn54Ile)	CALM1 (N54I +2 more)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 4	GLikely pathogenic
Select item 183232	NM_006888.6(CALM1):c.268T>C (p.Phe90Leu)	CALM1 (F90L +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 14	GLikely pathogenic
Select item 183230	NM_006888.6(CALM1):c.389A>G (p.Asp130Gly)	CALM1, LOC126862021 (D130G +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 974613	NM_006888.6(CALM1):c.422A>T (p.Glu141Val)	CALM1, LOC126862021 (E105V +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 14	GPathogenic
Select item 974612	NM_006888.6(CALM1):c.422A>G (p.Glu141Gly)	CALM1, LOC126862021 (E105G +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 14	GPathogenic
Select item 183231	NM_006888.6(CALM1):c.426C>G (p.Phe142Leu)	CALM1, LOC126862021 (F142L +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 14	GPathogenic

ClinVar