ClinVar for MedGen (Select 14047) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062000	NM_001379291.1(BRD4):c.703C>T (p.Gln235Ter)	BRD4 (Q235*)	Single nucleotide variant (nonsense)	Mental disorder	GLikely pathogenic
Select item 2671883	NM_001379291.1(BRD4):c.883A>C (p.Thr295Pro)	BRD4	Single nucleotide variant (missense variant)	Mental disorder	GUncertain significance
Select item 217510	NC_000002.10:g.[51151955_51190352del;51440969_51481281del]	NRXN1-DT	Deletion	Mental disorder	GUncertain significance

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