"PreventionGenetics, part of Exact Sciences"[submitter] AND "PCDHAC1"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 770914	NM_018903.4(PCDHA12):c.2492C>G (p.Pro831Arg)	PCDHA4, PCDHA6 +15 more (P576R +10 more)	Single nucleotide variant (missense variant)	PCDHA9-related disorder +1 more	GBenign/Likely benign
Select item 3044804	NM_018904.3(PCDHA13):c.2543-9_2543-8del	PCDHA1, PCDHA10 +15 more	Deletion (intron variant)	PCDHA13-related disorder	GLikely benign
Select item 3044886	NM_018904.3(PCDHA13):c.2802C>T (p.Thr934=)	PCDHA1, PCDHA10 +15 more	Single nucleotide variant (synonymous variant)	PCDHA13-related disorder	GBenign

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