"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "WEE2-AS1"[ - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1175771	NM_001105558.1(WEE2):c.1069G>A (p.Gly357Arg)	WEE2, WEE2-AS1 (G357R)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GUncertain significance
Select item 1013566	NM_001105558.1(WEE2):c.1350C>T (p.Asp450=)	WEE2, WEE2-AS1	Single nucleotide variant (synonymous variant)	WEE2-related condition +1 more	GLikely benign
Select item 1335693	NM_001105558.1(WEE2):c.1459C>T (p.Arg487Trp)	WEE2, WEE2-AS1 (R487W)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance

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