C5676967[trait identifier] AND "Neuberg Centre For Genomic Medicine, N - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1010621	NM_001258392.3(CLPB):c.748C>T (p.Arg250Cys)	CLPB (R221C +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 3236439	NM_001258392.3(CLPB):c.374A>G (p.His125Arg)	CLPB (H125R)	Single nucleotide variant (missense variant +1 more)	3-methylglutaconic aciduria, type VIIA	GUncertain significance