"Ambry Genetics"[submitter] AND "LOC126863139"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2241764	NM_001177701.3(IFT27):c.226G>T (p.Asp76Tyr)	CACNG2-DT, IFT27 +1 more (D75Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2536471	NM_001177701.3(IFT27):c.203A>C (p.Lys68Thr)	CACNG2-DT, IFT27 +1 more (K67T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance