List of variants in gene SCN1B reported as pathogenic for Brugada syndrome 5

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001037.5(SCN1B):c.265C>T (p.Arg89Cys)	rs766910280	0.00004
NM_001037.5(SCN1B):c.363C>G (p.Cys121Trp)	rs104894718	0.00003
NM_001037.5(SCN1B):c.254G>A (p.Arg85His)	rs16969925	0.00002
NM_001037.5(SCN1B):c.3G>C (p.Met1Ile)	rs2064208424	0.00001
NM_001037.5(SCN1B):c.448+88G>A	rs267607028	0.00001
NM_001037.5(SCN1B):c.105del (p.Phe36fs)
NM_001037.5(SCN1B):c.178dup (p.Arg60fs)
NM_001037.5(SCN1B):c.1A>C (p.Met1Leu)	rs1375857363
NM_001037.5(SCN1B):c.207+1G>A	rs2064222084
NM_001037.5(SCN1B):c.253C>T (p.Arg85Cys)	rs786205830
NM_001037.5(SCN1B):c.2T>C (p.Met1Thr)	rs2151745332
NM_001037.5(SCN1B):c.312_315del (p.Ile106fs)
NM_001037.5(SCN1B):c.347del (p.Ser116fs)	rs794727487
NM_001037.5(SCN1B):c.3G>A (p.Met1Ile)
NM_001037.5(SCN1B):c.472G>A (p.Val158Met)	rs138450474
NM_001037.5(SCN1B):c.518G>A (p.Trp173Ter)
NM_001037.5(SCN1B):c.59dup (p.Cys21fs)
NM_001037.5(SCN1B):c.94_95insC (p.Tyr32fs)

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