"Genome-Nilou Lab"[submitter] AND "CDH11"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1192547	NM_001797.4(CDH11):c.1642+20C>T	CDH11	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1192548	NM_001797.4(CDH11):c.1253+43G>C	CDH11	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1192549	NM_001797.4(CDH11):c.1117T>G (p.Ser373Ala)	CDH11 (S247A +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1192581	NM_001797.4(CDH11):c.945G>A (p.Ser315=)	CDH11	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1192582	NM_001797.4(CDH11):c.825G>A (p.Met275Ile)	CDH11 (M149I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1179215	NM_001797.4(CDH11):c.811+13A>G	CDH11	Single nucleotide variant (intron variant)	Elsahy-Waters syndrome +1 more	GBenign
Select item 1192583	NM_001797.4(CDH11):c.764C>T (p.Thr255Met)	CDH11 (T129M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1192584	NM_001797.4(CDH11):c.644-11T>C	CDH11	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

ClinVar