"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PCDHGA11"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2655863	NM_003735.3(PCDHGA12):c.1110T>C (p.Asn370=)	PCDHG@, PCDHGA1 +18 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655864	NM_003735.3(PCDHGA12):c.1656G>A (p.Val552=)	PCDHG@, PCDHGA1 +18 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655865	NM_003736.4(PCDHGB4):c.2397+42563A>G	PCDHG@, PCDHGA1 +18 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3025035	NM_018928.3(PCDHGC4):c.1955G>T (p.Ser652Ile)	PCDHGC4, PCDHGB5 +20 more (S652I)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2655866	NM_018928.3(PCDHGC4):c.2092G>C (p.Val698Leu)	PCDHG@, PCDHGA1 +20 more (V698L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2655867	NM_018912.3(PCDHGA1):c.2502C>T (p.Thr834=)	PCDHG@, PCDHGA1 +21 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 425542	GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3	ARL10, ARL14EPL +511 more	Copy number gain	not provided	GLikely benign

ClinVar