"Ambry Genetics"[submitter] AND "LOC130002815"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3276831	NM_014285.7(EXOSC2):c.86C>T (p.Pro29Leu)	EXOSC2, LOC130002815 (P29L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311789	NM_014285.7(EXOSC2):c.97A>G (p.Ile33Val)	EXOSC2, LOC130002815 (I33V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance