"Ambry Genetics"[submitter] AND "LOC126861730"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2616362	NM_023037.3(FRY):c.4510G>A (p.Val1504Met)	FRY, LOC126861730 (V1504M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475353	NM_023037.3(FRY):c.4568G>A (p.Ser1523Asn)	FRY, LOC126861730 (S1523N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance