"Ambry Genetics"[submitter] AND "DTD2"[gene] - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3086053	NM_080664.3(DTD2):c.445G>A (p.Gly149Arg)	DTD2, HEATR5A-DT (G149R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367860	NM_080664.3(DTD2):c.443A>G (p.Tyr148Cys)	DTD2, HEATR5A-DT (Y148C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273943	NM_080664.3(DTD2):c.37C>T (p.Leu13Phe)	DTD2 (L13F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

Format

Sort by

Choose Destination

ClinVar