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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2659473	NM_007018.6(CNTRL):c.1455G>A (p.Lys485=)	CNTRL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2659474	NM_007018.6(CNTRL):c.4224A>G (p.Glu1408=)	CNTRL	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2659475	NM_007018.6(CNTRL):c.5809G>A (p.Glu1937Lys)	CNTRL (E1385K +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign

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