"Ambry Genetics"[submitter] AND "LOC130005046"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2066198	NM_001025295.3(IFITM5):c.196C>G (p.Gln66Glu)	IFITM5, LOC130005046 (Q66E)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2704259	NM_001025295.3(IFITM5):c.191G>A (p.Arg64Gln)	IFITM5, LOC130005046 (R64Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity