"Neuberg Centre For Genomic Medicine, NCGM"[submitter] AND "CCNF"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2585153	NM_001761.3(CCNF):c.62G>A (p.Arg21Gln)	CCNF (R21Q)	Single nucleotide variant (5 prime UTR variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5	GUncertain significance
Select item 2627498	NM_001761.3(CCNF):c.436G>A (p.Ala146Thr)	CCNF (A146T)	Single nucleotide variant (5 prime UTR variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 5	GUncertain significance