"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC126862860"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 193976	NM_000159.4(GCDH):c.1244-2A>C	GCDH, LOC126862860 +1 more	Single nucleotide variant (splice acceptor variant +1 more)	not provided +1 more	GPathogenic
Select item 2082	NM_000159.4(GCDH):c.1262C>T (p.Ala421Val)	GCDH, LOC126862860 +1 more (A421V)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GPathogenic