C1394891[trait identifier] AND "Inserm U 954, Faculté de Médecine de N - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 208192	NM_005142.3(CBLIF):c.432GAA[1] (p.Lys145del)	CBLIF (K145del)	Microsatellite (inframe_deletion)	Hereditary intrinsic factor deficiency	GLikely benign
Select item 208191	NM_005142.3(CBLIF):c.346C>T (p.Gln116Ter)	CBLIF (Q116*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 208190	NM_005142.2(CBLIF):c.-376A>T	CBLIF	Single nucleotide variant	Hereditary intrinsic factor deficiency	Gnot provided

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