"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "CYP26C1"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 496732	NM_183374.3(CYP26C1):c.845_851dup (p.Gln284fs)	CYP26C1 (Q284fs)	Duplication (frameshift variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 3025146	NM_183374.3(CYP26C1):c.862G>A (p.Glu288Lys)	CYP26C1 (E288K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2640681	NM_183374.3(CYP26C1):c.1260G>A (p.Val420=)	CYP26C1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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ClinVar