"Ambry Genetics"[submitter] AND "LOC130058296"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2516446	NM_022468.5(MMP25):c.1080G>C (p.Trp360Cys)	LOC130058296, MMP25 +1 more (W360C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2255587	NM_022468.5(MMP25):c.1094C>G (p.Ala365Gly)	LOC130058296, MMP25 +1 more (A365G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance