"Eurofins Ntd Llc (ga)"[submitter] AND "HOMER2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 594584	NM_004839.4(HOMER2):c.763-8del	HOMER2	Deletion (intron variant)	not provided	GConflicting classifications of pathogenicity
Select item 508119	NM_004839.4(HOMER2):c.651+9G>A	HOMER2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 500298	NM_004839.4(HOMER2):c.643C>T (p.Arg215Cys)	HOMER2 (R215C +1 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 500844	NM_004839.4(HOMER2):c.609G>T (p.Gln203His)	HOMER2 (Q203H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 501014	NM_004839.4(HOMER2):c.363C>T (p.Ile121=)	HOMER2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 500053	NM_004839.4(HOMER2):c.33G>A (p.Ala11=)	HOMER2	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity

ClinVar