"Baylor Genetics"[submitter] AND "NECTIN4"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1029983	NM_030916.3(NECTIN4):c.1478G>C (p.Arg493Pro)	NECTIN4 (R493P)	Single nucleotide variant (missense variant)	Ectodermal dysplasia-syndactyly syndrome 1	GUncertain significance
Select item 1032240	NM_030916.3(NECTIN4):c.1387C>G (p.Pro463Ala)	NECTIN4 (P463A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 625771	GRCh37/hg19 1q23.2-25.1(chr1:160369890-175796325)	ADCY10, ALDH9A1 +137 more	Copy number loss	not provided	GPathogenic

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ClinVar