List of variants in gene CDH1 reported as uncertain significance by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1996A>C (p.Asn666His)	rs150427791	0.00009
NM_004360.5(CDH1):c.854C>T (p.Thr285Ile)	rs587781634	0.00007
NM_004360.5(CDH1):c.214G>A (p.Asp72Asn)	rs35606263	0.00006
NM_004360.5(CDH1):c.2387G>A (p.Arg796Gln)	rs587782549	0.00004
NM_004360.5(CDH1):c.1417G>A (p.Val473Ile)	rs36087757	0.00003
NM_004360.5(CDH1):c.2074G>A (p.Ala692Thr)	rs376854556	0.00003
NM_004360.5(CDH1):c.1004G>A (p.Arg335Gln)	rs373364873	0.00002
NM_004360.5(CDH1):c.1679C>T (p.Thr560Met)	rs746481984	0.00002
NM_004360.5(CDH1):c.2359G>A (p.Val787Ile)	rs766270336	0.00002
NM_004360.5(CDH1):c.371G>A (p.Arg124His)	rs115418995	0.00002
NM_004360.5(CDH1):c.1136C>T (p.Thr379Met)	rs587782856	0.00001
NM_004360.5(CDH1):c.2332G>A (p.Ala778Thr)	rs777078601	0.00001
NM_004360.5(CDH1):c.2351G>A (p.Arg784His)	rs763203357	0.00001
NM_004360.5(CDH1):c.2530A>T (p.Ser844Cys)	rs761400928	0.00001
NM_004360.5(CDH1):c.254T>C (p.Val85Ala)	rs878854688	0.00001
NM_004360.5(CDH1):c.2638G>A (p.Glu880Lys)	rs34507583	0.00001
NM_004360.5(CDH1):c.79C>T (p.Pro27Ser)	rs878854696	0.00001
NM_004360.5(CDH1):c.1008+8G>T	rs990193541
NM_004360.5(CDH1):c.1264C>A (p.Gln422Lys)	rs2152133566
NM_004360.5(CDH1):c.1468G>A (p.Glu490Lys)	rs1555516147
NM_004360.5(CDH1):c.1721T>G (p.Val574Gly)	rs1567512117
NM_004360.5(CDH1):c.1784C>G (p.Pro595Arg)	rs1555516843
NM_004360.5(CDH1):c.1937-4C>T	rs1057523153
NM_004360.5(CDH1):c.2098C>G (p.Pro700Ala)	rs878854681
NM_004360.5(CDH1):c.2204C>A (p.Ala735Glu)	rs587782464
NM_004360.5(CDH1):c.2467A>G (p.Thr823Ala)	rs878854686
NM_004360.5(CDH1):c.2518T>C (p.Ser840Pro)	rs1555518243
NM_004360.5(CDH1):c.2560G>A (p.Asp854Asn)	rs1555518257
NM_004360.5(CDH1):c.29C>A (p.Ala10Glu)	rs1375360857
NM_004360.5(CDH1):c.32T>G (p.Leu11Arg)	rs1393903966
NM_004360.5(CDH1):c.417G>C (p.Leu139Phe)	rs1057521858
NM_004360.5(CDH1):c.778C>T (p.Pro260Ser)	rs1567505715
NM_004360.5(CDH1):c.949T>C (p.Phe317Leu)	rs1555515643
NM_004360.5(CDH1):c.976A>G (p.Ile326Val)	rs1567506764

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