"CDH11-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043027	NM_001797.4(CDH11):c.*8G>C	CDH11	Single nucleotide variant (3 prime UTR variant)	CDH11-related disorder	GLikely benign
Select item 3060946	NM_001797.4(CDH11):c.*7C>T	CDH11	Single nucleotide variant (3 prime UTR variant)	CDH11-related disorder	GLikely benign
Select item 3025636	NM_001797.4(CDH11):c.2073C>G (p.Ile691Met)	CDH11 (I565M +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	CDH11-related disorder +1 more	GBenign/Likely benign
Select item 3033576	NM_001797.4(CDH11):c.1895-503C>G	CDH11	Single nucleotide variant (intron variant)	CDH11-related disorder	GLikely benign
Select item 2633487	NM_001797.4(CDH11):c.1895-569dup	CDH11 (V672fs)	Duplication (frameshift variant +1 more)	CDH11-related disorder	GUncertain significance
Select item 3056278	NM_001797.4(CDH11):c.1039G>C (p.Val347Leu)	CDH11 (V221L +1 more)	Single nucleotide variant (missense variant)	CDH11-related disorder	GBenign
Select item 3038846	NM_001797.4(CDH11):c.198C>T (p.Tyr66=)	CDH11	Single nucleotide variant (synonymous variant +1 more)	CDH11-related disorder	GLikely benign

ClinVar