"Ambry Genetics"[submitter] AND "LOC130056355"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290558	NM_005606.7(LGMN):c.1237G>C (p.Glu413Gln)	LGMN, LOC130056355 (E356Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349549	NM_005606.7(LGMN):c.1219G>A (p.Val407Met)	LGMN, LOC130056355 (V350M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance