"Ambry Genetics"[submitter] AND "LOC101927418"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2398402	NM_001017923.2(C14orf28):c.443C>T (p.Ser148Phe)	LOC101927418, C14orf28 (S148F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2229588	NM_001017923.2(C14orf28):c.844C>T (p.Leu282Phe)	C14orf28, LOC101927418 (L282F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance