ClinVar Miner

List of variants reported as uncertain significance for EEM syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 54
Download table as spreadsheet
HGVS dbSNP
NM_001793.5(CDH3):c.-1085A>G rs768872455
NM_001793.5(CDH3):c.-140G>T rs886052227
NM_001793.5(CDH3):c.-141C>G rs537339409
NM_001793.5(CDH3):c.-193G>T rs550203444
NM_001793.5(CDH3):c.-267C>T rs182969772
NM_001793.5(CDH3):c.-282G>T rs886052226
NM_001793.5(CDH3):c.-302C>T rs145687049
NM_001793.5(CDH3):c.-621G>A rs886052225
NM_001793.5(CDH3):c.-626_-620delAAAAAGA rs886052223
NM_001793.5(CDH3):c.-628G>A rs796187375
NM_001793.5(CDH3):c.-634_-633insG rs886052224
NM_001793.5(CDH3):c.-635_-634insG rs886052222
NM_001793.5(CDH3):c.-646_-645insA rs886052221
NM_001793.5(CDH3):c.-679T>C rs150247850
NM_001793.5(CDH3):c.-72T>C rs557660477
NM_001793.5(CDH3):c.-983A>G rs151123159
NM_001793.6(CDH3):c.*405G>A rs778268579
NM_001793.6(CDH3):c.*485A>G rs192275133
NM_001793.6(CDH3):c.*498G>A rs746152331
NM_001793.6(CDH3):c.*529G>A rs886052235
NM_001793.6(CDH3):c.*595G>A rs111487714
NM_001793.6(CDH3):c.*87G>C rs555473968
NM_001793.6(CDH3):c.-11T>C rs370893872
NM_001793.6(CDH3):c.-36C>T rs373351410
NM_001793.6(CDH3):c.100G>A (p.Ala34Thr) rs749754991
NM_001793.6(CDH3):c.1011G>C (p.Val337=) rs201726457
NM_001793.6(CDH3):c.1043G>A (p.Arg348Lys) rs886052231
NM_001793.6(CDH3):c.1178G>A (p.Arg393Lys) rs766325919
NM_001793.6(CDH3):c.1183-12C>T rs886052232
NM_001793.6(CDH3):c.1240G>A (p.Ala414Thr) rs145203128
NM_001793.6(CDH3):c.1339G>A (p.Val447Ile) rs145160881
NM_001793.6(CDH3):c.1436T>C (p.Leu479Pro) rs138190335
NM_001793.6(CDH3):c.1443C>T (p.Asp481=) rs144403828
NM_001793.6(CDH3):c.1500C>T (p.Thr500=) rs35232945
NM_001793.6(CDH3):c.1571-7C>G rs373529822
NM_001793.6(CDH3):c.1593G>A (p.Thr531=) rs147208782
NM_001793.6(CDH3):c.166A>G (p.Met56Val) rs886052228
NM_001793.6(CDH3):c.1681G>A (p.Val561Met) rs151198926
NM_001793.6(CDH3):c.1740G>C (p.Gln580His) rs886052233
NM_001793.6(CDH3):c.1796-11G>T rs752252704
NM_001793.6(CDH3):c.1848C>T (p.Asp616=) rs768811436
NM_001793.6(CDH3):c.1932C>T (p.Val644=) rs750805163
NM_001793.6(CDH3):c.2042G>A (p.Arg681Gln) rs758614807
NM_001793.6(CDH3):c.2070A>G (p.Pro690=) rs886052234
NM_001793.6(CDH3):c.2361C>T (p.Ser787=) rs201352240
NM_001793.6(CDH3):c.2419G>A (p.Asp807Asn) rs535174122
NM_001793.6(CDH3):c.2444G>A (p.Arg815His) rs557740168
NM_001793.6(CDH3):c.2484C>T (p.Asp828=) rs202210726
NM_001793.6(CDH3):c.318G>A (p.Lys106=) rs886052229
NM_001793.6(CDH3):c.390+5G>A rs570628442
NM_001793.6(CDH3):c.691G>C (p.Gly231Arg) rs886052230
NM_001793.6(CDH3):c.805A>C (p.Met269Leu) rs36038900
NM_001793.6(CDH3):c.867+6T>C rs753122508
NM_001793.6(CDH3):c.886C>G (p.Leu296Val) rs565345878

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.