"Genome Diagnostics Laboratory, The Hospital for Sick Children"[submit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1712435	NM_178170.3(NEK8):c.453C>T (p.Ser151=)	NEK8	Single nucleotide variant (synonymous variant)	Kidney disorder	GUncertain significance
Select item 539144	NM_178170.3(NEK8):c.1237A>C (p.Met413Leu)	NEK8 (M413L)	Single nucleotide variant (missense variant)	Kidney disorder +2 more	GConflicting classifications of pathogenicity
Select item 242154	NM_178170.3(NEK8):c.1732+8_1732+10del	NEK8	Microsatellite (intron variant)	Nephronophthisis 9 +3 more	GBenign/Likely benign

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