"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC110121 - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3046912	NM_006514.4(SCN10A):c.3507+6G>A	LOC110121288, SCN10A	Single nucleotide variant (intron variant)	SCN10A-related disorder	GLikely benign
Select item 1034930	NM_006514.4(SCN10A):c.3394A>C (p.Lys1132Gln)	LOC110121288, SCN10A (K1034Q +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +2 more	GConflicting classifications of pathogenicity
Select item 259998	NM_006514.4(SCN10A):c.3393C>G (p.Thr1131=)	LOC110121288, SCN10A	Single nucleotide variant (synonymous variant)	Episodic pain syndrome, familial, 2 +3 more	GBenign
Select item 3030262	NM_006514.4(SCN10A):c.3353-5C>T	LOC110121288, SCN10A	Single nucleotide variant (intron variant)	SCN10A-related disorder	GLikely benign
Select item 259997	NM_006514.4(SCN10A):c.3275T>C (p.Leu1092Pro)	LOC110121288, SCN10A (L1092P +2 more)	Single nucleotide variant (missense variant)	Episodic pain syndrome, familial, 2 +3 more	GBenign/Likely benign
Select item 259996	NM_006514.4(SCN10A):c.3218T>C (p.Val1073Ala)	LOC110121288, SCN10A (V1073A +2 more)	Single nucleotide variant (missense variant)	Brugada syndrome +3 more	GBenign
Select item 259995	NM_006514.4(SCN10A):c.3192G>A (p.Thr1064=)	LOC110121288, SCN10A	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GBenign
Select item 259994	NM_006514.4(SCN10A):c.2937C>T (p.Gly979=)	LOC110121288, SCN10A	Single nucleotide variant (synonymous variant)	Episodic pain syndrome, familial, 2 +3 more	GBenign
Select item 95401	NM_006514.4(SCN10A):c.2884A>G (p.Ile962Val)	LOC110121288, SCN10A (I962V +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign