"Genome-Nilou Lab"[submitter] AND "ERBB4"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1210000	NM_005235.3(ERBB4):c.1490-15T>C	ERBB4	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 770696	NM_005235.3(ERBB4):c.1122T>G (p.His374Gln)	ERBB4 (H374Q)	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis +2 more	GConflicting classifications of pathogenicity
Select item 769264	NM_005235.3(ERBB4):c.884-7del	ERBB4	Deletion (intron variant)	not specified +2 more	GBenign

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