"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "CDC27"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2647872	NM_001256.6(CDC27):c.1758A>G (p.Ala586=)	CDC27	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 782550	NM_001256.6(CDC27):c.858A>G (p.Pro286=)	CDC27	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign/Likely benign
Select item 2647873	NM_001256.6(CDC27):c.501A>T (p.Thr167=)	CDC27	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign

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