C4748688[trait identifier] AND "Center for Genomic Medicine, King Fais - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1388245	NM_001042646.3(TRAK1):c.920A>G (p.Glu307Gly)	TRAK1 (E233G +3 more)	Single nucleotide variant (missense variant +1 more)	Developmental and epileptic encephalopathy, 68 +1 more	GUncertain significance
Select item 3068224	NM_001042646.3(TRAK1):c.2762_2763insGAA (p.Pro921_Thr922insAsn)	TRAK1	Insertion (inframe_insertion +3 more)	Developmental and epileptic encephalopathy, 68	GUncertain significance