"Database of Curated Mutations (DoCM)"[submitter] AND "ERBB4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376170	NM_005235.3(ERBB4):c.2614G>A (p.Glu872Lys)	ERBB4 (E872K)	Single nucleotide variant (missense variant)	Melanoma	GLikely pathogenic
Select item 74426	NM_005235.3(ERBB4):c.1630C>T (p.Arg544Trp)	ERBB4 (R544W)	Single nucleotide variant (missense variant)	Melanoma	GLikely pathogenic
Select item 376171	NM_005235.3(ERBB4):c.1624G>A (p.Glu542Lys)	ERBB4 (E542K)	Single nucleotide variant (missense variant)	Melanoma	GLikely pathogenic
Select item 91898	NM_005235.3(ERBB4):c.1354G>A (p.Glu452Lys)	ERBB4 (E452K)	Single nucleotide variant (missense variant)	Melanoma	GLikely pathogenic
Select item 376172	NM_005235.3(ERBB4):c.1177C>T (p.Arg393Trp)	ERBB4 (R393W)	Single nucleotide variant (missense variant)	Melanoma	GLikely pathogenic
Select item 74427	NM_005235.3(ERBB4):c.949G>A (p.Glu317Lys)	ERBB4 (E317K)	Single nucleotide variant (missense variant)	Melanoma	GLikely pathogenic

ClinVar