"Ambry Genetics"[submitter] AND "LOC129999451"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2360429	NM_015905.3(TRIM24):c.44C>T (p.Ala15Val)	LOC129999451, TRIM24 (A15V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2384345	NM_015905.3(TRIM24):c.55G>C (p.Ala19Pro)	LOC129999451, TRIM24 (A19P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance