"Genetic Testing Center for Deafness, Department of Otolaryngology Hea - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 689607	NM_014208.3(DSPP):c.1031C>A (p.Thr344Asn)	DSPP (T344N)	Single nucleotide variant (missense variant)	Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 +1 more	GConflicting classifications of pathogenicity
Select item 627439	NM_014208.3(DSPP):c.3248_3249insC (p.Glu1083fs)	DSPP (E1083fs)	Insertion (frameshift variant)	Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1	GLikely pathogenic