"Eurofins Ntd Llc (ga)"[submitter] AND "SCN10A"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 95405	NM_006514.4(SCN10A):c.5657C>T (p.Ala1886Val)	SCN10A (A1886V +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +4 more	GBenign/Likely benign
Select item 95404	NM_006514.4(SCN10A):c.4866T>C (p.Ser1622=)	SCN10A	Single nucleotide variant (synonymous variant)	Brugada syndrome +4 more	GBenign
Select item 95403	NM_006514.4(SCN10A):c.4710G>A (p.Thr1570=)	SCN10A	Single nucleotide variant (synonymous variant)	Brugada syndrome +3 more	GBenign
Select item 95402	NM_006514.4(SCN10A):c.3859G>A (p.Val1287Ile)	SCN10A (V1287I +2 more)	Single nucleotide variant (missense variant)	Episodic pain syndrome, familial, 2 +3 more	GConflicting classifications of pathogenicity
Select item 95401	NM_006514.4(SCN10A):c.2884A>G (p.Ile962Val)	LOC110121288, SCN10A (I962V +1 more)	Single nucleotide variant (missense variant)	Brugada syndrome +4 more	GBenign/Likely benign
Select item 95400	NM_006514.4(SCN10A):c.1453C>T (p.Arg485Cys)	SCN10A (R485C)	Single nucleotide variant (missense variant)	Brugada syndrome +3 more	GBenign/Likely benign

ClinVar