"Clinical Genetics, Academic Medical Center"[submitter] AND "SCN4B"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 139036	NM_174934.4(SCN4B):c.639C>T (p.Asn213=)	SCN4B	Single nucleotide variant (synonymous variant +1 more)	Long QT syndrome 10 +3 more	GBenign
Select item 190895	NM_174934.4(SCN4B):c.632C>G (p.Thr211Arg)	SCN4B (T211R +2 more)	Single nucleotide variant (missense variant +1 more)	Long QT syndrome 10 +2 more	GConflicting classifications of pathogenicity
Select item 517068	NM_174934.4(SCN4B):c.378G>A (p.Thr126=)	SCN4B, LOC126861356	Single nucleotide variant (synonymous variant +1 more)	Cardiovascular phenotype +3 more	GLikely benign
Select item 1284803	NM_174934.4(SCN4B):c.208T>C (p.Tyr70His)	SCN4B (Y70H)	Single nucleotide variant (5 prime UTR variant +3 more)	not provided	GUncertain significance
Select item 139037	NM_174934.4(SCN4B):c.174C>T (p.Cys58=)	SCN4B	Single nucleotide variant (5 prime UTR variant +3 more)	Congenital long QT syndrome +3 more	GBenign/Likely benign
Select item 190889	NM_174934.4(SCN4B):c.18C>A (p.Asp6Glu)	SCN4B (D6E)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity

ClinVar