"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ADCY9"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2646144	NM_001116.4(ADCY9):c.3493G>A (p.Val1165Ile)	ADCY9 (V1165I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 769893	NM_001116.4(ADCY9):c.2994C>T (p.Arg998=)	ADCY9	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2646145	NM_001116.4(ADCY9):c.2898G>C (p.Ser966=)	ADCY9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 782311	NM_001116.4(ADCY9):c.2828+4C>G	ADCY9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2646146	NM_001116.4(ADCY9):c.1578C>T (p.Ala526=)	ADCY9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3024595	GRCh37/hg19 16p13.3(chr16:2990033-4837646)x1	ADCY9, ANKS3 +52 more	Copy number loss	not provided	GPathogenic

ClinVar