"Ambry Genetics"[submitter] AND "GCLM"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3281024	NM_002061.4(GCLM):c.720C>A (p.His240Gln)	GCLM (H240Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355643	NM_002061.4(GCLM):c.421G>C (p.Glu141Gln)	GCLM (E119Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265947	NM_002061.4(GCLM):c.406G>C (p.Val136Leu)	GCLM (V136L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281023	NM_002061.4(GCLM):c.113C>T (p.Thr38Met)	GCLM, LOC129930969 (T38M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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