"Ambry Genetics"[submitter] AND "HMGB3"[gene] - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2247329	NM_005342.4(HMGB3):c.86A>G (p.Lys29Arg)	HMGB3 (K29R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2276365	NM_005342.4(HMGB3):c.116C>T (p.Ala39Val)	HMGB3 (A39V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273567	NM_005342.4(HMGB3):c.493A>C (p.Lys165Gln)	HMGB3 (K165Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

Format

Sort by

Choose Destination

ClinVar