"Illumina Laboratory Services, Illumina"[submitter] AND "LOC126860216" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 136820	NM_014141.6(CNTNAP2):c.2895C>A (p.Gly965=)	CNTNAP2, LOC126860216	Single nucleotide variant (synonymous variant)	Cortical dysplasia-focal epilepsy syndrome +2 more	GBenign/Likely benign
Select item 909391	NM_014141.6(CNTNAP2):c.2903C>T (p.Thr968Ile)	CNTNAP2, LOC126860216 (T968I)	Single nucleotide variant (missense variant)	Cortical dysplasia-focal epilepsy syndrome	GUncertain significance