"Human Genetics Bochum, Ruhr University Bochum"[submitter] AND "ERBB4" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1801687	NM_005235.3(ERBB4):c.3494C>G (p.Pro1165Arg)	ERBB4 (P1149R +1 more)	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis type 10	GUncertain significance
Select item 1424254	NM_005235.3(ERBB4):c.1441A>G (p.Ile481Val)	ERBB4 (I481V)	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis type 10 +1 more	GUncertain significance