"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ERBB4"[gen - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 760722	NM_005235.3(ERBB4):c.3630C>T (p.Asn1210=)	ERBB4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1922637	NM_005235.3(ERBB4):c.3129G>A (p.Ser1043=)	ERBB4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 784585	NM_005235.3(ERBB4):c.2745C>T (p.Thr915=)	ERBB4	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 729304	NM_005235.3(ERBB4):c.2172T>C (p.Leu724=)	ERBB4	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2571116	NM_005235.3(ERBB4):c.1973T>C (p.Ile658Thr)	ERBB4 (I658T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1419117	NM_005235.3(ERBB4):c.1571G>A (p.Arg524His)	ERBB4 (R524H)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 2651862	NM_005235.3(ERBB4):c.1482A>G (p.Glu494=)	ERBB4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 726675	NM_005235.3(ERBB4):c.1170C>T (p.Asn390=)	ERBB4	Single nucleotide variant (synonymous variant)	ERBB4-related condition +1 more	GLikely benign
Select item 770696	NM_005235.3(ERBB4):c.1122T>G (p.His374Gln)	ERBB4 (H374Q)	Single nucleotide variant (missense variant)	Amyotrophic lateral sclerosis +3 more	GConflicting classifications of pathogenicity
Select item 2651863	NM_005235.3(ERBB4):c.884-9_884-7del	ERBB4	Deletion (intron variant)	not provided	GLikely benign
Select item 710418	NM_005235.3(ERBB4):c.882A>G (p.Pro294=)	ERBB4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 871310	NM_005235.3(ERBB4):c.731C>T (p.Thr244Ile)	ERBB4 (T244I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance