"Ambry Genetics"[submitter] AND "CCL20"[gene] - 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 2376820	NM_004591.3(CCL20):c.152G>A (p.Arg51Gln)	CCL20 (R50Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2460715	NM_004591.3(CCL20):c.182A>G (p.Asn61Ser)	CCL20 (N61S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139723	NM_004591.3(CCL20):c.260G>A (p.Arg87His)	CCL20 (R86H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

Format

Sort by

Choose Destination