C4015519[trait identifier] AND "OMIM"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 180246	NM_016373.3(WWOX):c.-366-?_516+?del	WWOX, LOC132090428 +1 more	Deletion	Developmental and epileptic encephalopathy, 28	GPathogenic
Select item 180250	NM_016373.4(WWOX):c.46_49del (p.Asp16fs)	WWOX (D16fs)	Deletion (5 prime UTR variant +2 more)	Developmental and epileptic encephalopathy, 1 +1 more	GPathogenic
Select item 180251	NM_016373.4(WWOX):c.140C>G (p.Pro47Arg)	WWOX (P47R)	Single nucleotide variant (missense variant +2 more)	Developmental and epileptic encephalopathy, 28	GPathogenic
Select item 120325	NM_016373.4(WWOX):c.160C>T (p.Arg54Ter)	WWOX (R54*)	Single nucleotide variant (nonsense +2 more)	Developmental and epileptic encephalopathy, 1 +2 more	GPathogenic
Select item 180248	NM_016373.4(WWOX):c.516+62335_517-3413del	LOC125177355, LOC132090431 +5 more	Deletion	Developmental and epileptic encephalopathy, 28	GPathogenic
Select item 180247	NM_016373.4(WWOX):c.517-44258_606-268del	WWOX	Deletion	Developmental and epileptic encephalopathy, 28	GPathogenic
Select item 180249	NM_016373.4(WWOX):c.1005G>A (p.Trp335Ter)	WWOX (W335* +1 more)	Single nucleotide variant (nonsense)	Developmental and epileptic encephalopathy, 28	GPathogenic

ClinVar