ClinVar Miner

List of variants in gene TJP2 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_004817.4(TJP2):c.1056+73C>A
NM_004817.4(TJP2):c.1137A>G (p.Leu379=) rs17062695
NM_004817.4(TJP2):c.1350C>T (p.Ser450=) rs17062723
NM_004817.4(TJP2):c.1446C>A (p.Asp482Glu) rs2309428
NM_004817.4(TJP2):c.1478G>A (p.Arg493Lys) rs41277901
NM_004817.4(TJP2):c.1917C>T (p.Asp639=) rs12340440
NM_004817.4(TJP2):c.2004G>A (p.Met668Ile) rs34774441
NM_004817.4(TJP2):c.2131T>C (p.Ser711Pro) rs35797487
NM_004817.4(TJP2):c.2715C>T (p.Thr905=) rs2282336
NM_004817.4(TJP2):c.2727G>A (p.Ala909=) rs2095876
NM_004817.4(TJP2):c.3029C>T (p.Ser1010Phe) rs41277907
NM_004817.4(TJP2):c.3407+45A>G
NM_004817.4(TJP2):c.342+12G>T rs7027812
NM_004817.4(TJP2):c.382C>A (p.Gln128Lys) rs41305539
NM_004817.4(TJP2):c.60+39CGTGAG[3]
NM_004817.4(TJP2):c.61-7316G>A rs4493966

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.