"Ambry Genetics"[submitter] AND "CLDN11"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2484094	NM_005602.6(CLDN11):c.508G>C (p.Val170Leu)	CLDN11 (V86L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472331	NM_005602.6(CLDN11):c.508G>A (p.Val170Met)	CLDN11 (V170M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322694	NM_005602.6(CLDN11):c.563A>G (p.Asn188Ser)	CLDN11 (N188S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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ClinVar