"Ambry Genetics"[submitter] AND "LOC130059325"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3091209	NM_058219.3(EXOSC6):c.290T>A (p.Leu97His)	EXOSC6, LOC130059325 (L97H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272458	NM_058219.3(EXOSC6):c.217G>C (p.Glu73Gln)	EXOSC6, LOC130059325 (E73Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance