"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ADCY10"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2724245	NM_018417.6(ADCY10):c.3864A>C (p.Lys1288Asn)	ADCY10 (K1196N +2 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 718045	NM_018417.6(ADCY10):c.3765C>T (p.Tyr1255=)	ADCY10	Single nucleotide variant (synonymous variant)	Familial idiopathic hypercalciuria +1 more	GBenign/Likely benign
Select item 787696	NM_018417.6(ADCY10):c.2565G>A (p.Lys855=)	ADCY10	Single nucleotide variant (synonymous variant)	ADCY10-related condition +1 more	GBenign/Likely benign
Select item 787530	NM_018417.6(ADCY10):c.2097A>G (p.Ala699=)	ADCY10	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 949727	NM_018417.6(ADCY10):c.1263C>A (p.Tyr421Ter)	ADCY10, DCAF6 (Y268* +2 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic/Likely pathogenic
Select item 2639530	NM_018417.6(ADCY10):c.1021-8C>T	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1901853	NM_018417.6(ADCY10):c.437-8C>G	ADCY10, DCAF6	Single nucleotide variant (intron variant)	not provided	GLikely benign

ClinVar