C5231489[trait identifier] AND "MVZ Medizinische Genetik Mainz"[submit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3236205	NM_001260.3(CDK8):c.185C>G (p.Ser62Trp)	CDK8 (S62W)	Single nucleotide variant (missense variant +1 more)	Intellectual developmental disorder with hypotonia and behavioral abnormalities	GLikely pathogenic
Select item 3234070	NM_001260.3(CDK8):c.398A>G (p.Tyr133Cys)	CDK8 (Y133C)	Single nucleotide variant (missense variant +1 more)	Intellectual developmental disorder with hypotonia and behavioral abnormalities	GUncertain significance