"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "CTTNBP2"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2657962	NM_033427.3(CTTNBP2):c.4757C>T (p.Pro1586Leu)	CTTNBP2 (P1568L +2 more)	Single nucleotide variant (missense variant)	CTTNBP2-related condition +1 more	GBenign
Select item 2657963	NM_033427.3(CTTNBP2):c.4278A>G (p.Thr1426=)	CTTNBP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657964	NM_033427.3(CTTNBP2):c.4056-5G>T	CTTNBP2	Single nucleotide variant (intron variant)	not provided	GLikely benign

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