C3281202[trait identifier] AND "Genetics and Molecular Pathology, SA P - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1803222	NM_001376.5(DYNC1H1):c.5557G>A (p.Val1853Met)	DYNC1H1 (V1853M)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 13	GUncertain significance
Select item 637520	NM_001376.5(DYNC1H1):c.7846G>A (p.Glu2616Lys)	DYNC1H1 (E2616K)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 13	GUncertain significance