"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "HUNK"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2652590	NM_014586.2(HUNK):c.1280G>A (p.Arg427Gln)	HUNK (R427Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2652591	NM_014586.2(HUNK):c.1539G>C (p.Val513=)	HUNK	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1711546	GRCh37/hg19 21q22.11(chr21:33032083-34809269)x3	CFAP298, EPCIP +17 more	Copy number gain	not provided	GUncertain significance

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