"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ERBB2"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 134090	NM_004448.4(ERBB2):c.428G>A (p.Arg143Gln)	ERBB2 (R113Q +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign/Likely benign
Select item 775162	NM_004448.4(ERBB2):c.528C>T (p.Asn176=)	ERBB2	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 376188	NM_004448.4(ERBB2):c.929C>A (p.Ser310Tyr)	ERBB2 (S280Y +7 more)	Single nucleotide variant (missense variant +1 more)	not provided	GPathogenic
Select item 13874	NM_004448.4(ERBB2):c.1960A>G (p.Ile654Val)	ERBB2 (I654V +13 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign/Likely benign
Select item 2647722	NM_004448.4(ERBB2):c.2967C>T (p.Ile989=)	ERBB2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1596027	NM_004448.4(ERBB2):c.3249C>A (p.Ser1083=)	ERBB2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2169163	NM_004448.4(ERBB2):c.3470T>G (p.Leu1157Arg)	ERBB2 (L1089R +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GConflicting classifications of pathogenicity
Select item 134084	NM_004448.4(ERBB2):c.3647C>A (p.Ala1216Asp)	ERBB2 (A1186D +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign/Likely benign

ClinVar