Related gene-specific medical variations for Gene (Select 150356) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3144008	NM_138481.2(CHADL):c.2272G>A (p.Glu758Lys)	CHADL, L3MBTL2 (E758K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117266	NM_031488.5(L3MBTL2):c.1913C>T (p.Thr638Met)	CHADL, L3MBTL2 (T638M)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2681366	NM_031488.5(L3MBTL2):c.2049G>A (p.Ser683=)	CHADL, L3MBTL2	Single nucleotide variant (synonymous variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2653221	NM_031488.5(L3MBTL2):c.2088C>T (p.Val696=)	CHADL, L3MBTL2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2588750	NM_031488.5(L3MBTL2):c.2018G>A (p.Arg673His)	CHADL, L3MBTL2 (R673H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512444	NM_031488.5(L3MBTL2):c.2017C>T (p.Arg673Cys)	CHADL, L3MBTL2 (R673C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383237	NM_031488.5(L3MBTL2):c.1991C>G (p.Pro664Arg)	CHADL, L3MBTL2 (P664R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2313117	NM_031488.5(L3MBTL2):c.2029G>A (p.Glu677Lys)	CHADL, L3MBTL2 (E677K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar