"OMIM"[submitter] AND "PDCD10"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 468332	NM_007217.4(PDCD10):c.557+4_557+7del	PDCD10	Microsatellite (splice donor variant)	Cerebral cavernous malformation 3	GPathogenic
Select item 1869	NM_007217.4(PDCD10):c.475-1G>A	PDCD10	Single nucleotide variant (splice acceptor variant)	Cerebral cavernous malformation 3	GPathogenic
Select item 1865	NM_007217.4(PDCD10):c.385C>T (p.Gln129Ter)	PDCD10 (Q129*)	Single nucleotide variant (nonsense)	Cerebral cavernous malformation 3	GPathogenic
Select item 372445	NM_007217.4(PDCD10):c.103C>T (p.Arg35Ter)	PDCD10 (R35*)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 1870	NC_000003.12:g.(?_167683298_(167734892_?)del	PDCD10	Deletion	Cerebral cavernous malformation 3	GPathogenic
Select item 1867	NM_007217.4(PDCD10):c.97_150del	PDCD10	Deletion (splice acceptor variant)	Cerebral cavernous malformation 3	GPathogenic

ClinVar