"Ambry Genetics"[submitter] AND "LOC129936713"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2236295	NM_003365.3(UQCRC1):c.91G>A (p.Ala31Thr)	LOC129936713, UQCRC1 (A31T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469062	NM_003365.3(UQCRC1):c.83G>T (p.Arg28Leu)	LOC129936713, UQCRC1 (R28L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186876	NM_003365.3(UQCRC1):c.76C>G (p.Leu26Val)	LOC129936713, UQCRC1 (L26V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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