"Ambry Genetics"[submitter] AND "LOC130058686"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2378476	NM_016309.3(LCMT1):c.32C>T (p.Thr11Ile)	LCMT1, LOC130058686 (T11I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118086	NM_016309.3(LCMT1):c.35C>T (p.Ser12Phe)	LCMT1, LOC130058686 (S12F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304745	NM_016309.3(LCMT1):c.67G>T (p.Asp23Tyr)	LCMT1, LOC130058686 (D23Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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