"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 158486	NM_001195553.2(DCX):c.588T>C (p.Arg196=)	DCX	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1285024	NM_001195553.2(DCX):c.540G>T (p.Lys180Asn)	DCX (K180N +1 more)	Single nucleotide variant (missense variant)	not provided	GPathogenic/Likely pathogenic
Select item 1285219	NM_001195553.2(DCX):c.429T>C (p.Asn143=)	DCX	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign

Format

Sort by

Choose Destination