List of variants in gene PDCD10 reported as likely benign for cerebral cavernous malformation 3

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_007217.4(PDCD10):c.395+46C>T	rs200959967	0.00353
NM_007217.4(PDCD10):c.*285G>T	rs190941416	0.00245
NM_007217.4(PDCD10):c.574G>A (p.Val192Ile)	rs151267430	0.00061
NM_007217.4(PDCD10):c.213C>T (p.Ser71=)	rs201316215	0.00001
NM_007217.4(PDCD10):c.45A>G (p.Thr15=)	rs751478724	0.00001
NM_007217.4(PDCD10):c.96+17T>C	rs1208666143	0.00001
NM_007217.4(PDCD10):c.150+11A>G
NM_007217.4(PDCD10):c.159A>G (p.Lys53=)
NM_007217.4(PDCD10):c.268+18del
NM_007217.4(PDCD10):c.270G>A (p.Glu90=)
NM_007217.4(PDCD10):c.312C>T (p.Asn104=)
NM_007217.4(PDCD10):c.396-19T>C
NM_007217.4(PDCD10):c.475-4del	rs772163237
NM_007217.4(PDCD10):c.475-8G>A
NM_007217.4(PDCD10):c.573C>T (p.Phe191=)

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