ClinVar Miner

List of variants in gene CDHR1 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
Download table as spreadsheet
HGVS dbSNP
NM_033100.4(CDHR1):c.1071C>T (p.Ser357=) rs146588811
NM_033100.4(CDHR1):c.1133G>A (p.Arg378Gln) rs140621272
NM_033100.4(CDHR1):c.1357A>G (p.Ser453Gly) rs886044615
NM_033100.4(CDHR1):c.1461G>A (p.Gly487=) rs141787212
NM_033100.4(CDHR1):c.1471G>A (p.Val491Met) rs138638103
NM_033100.4(CDHR1):c.1553+6T>C rs199567321
NM_033100.4(CDHR1):c.1700T>C (p.Leu567Pro) rs1064797147
NM_033100.4(CDHR1):c.1868A>G (p.Asn623Ser) rs137876961
NM_033100.4(CDHR1):c.1877C>T (p.Thr626Met) rs143024855
NM_033100.4(CDHR1):c.1978G>A (p.Asp660Asn) rs1085307801
NM_033100.4(CDHR1):c.1A>G (p.Met1Val) rs794726954
NM_033100.4(CDHR1):c.2176C>T (p.Arg726Cys) rs141706561
NM_033100.4(CDHR1):c.2218C>T (p.Leu740Phe) rs762396052
NM_033100.4(CDHR1):c.2229G>A (p.Arg743=) rs150969538
NM_033100.4(CDHR1):c.2470C>T (p.Gln824Ter) rs762298688
NM_033100.4(CDHR1):c.415C>G (p.Pro139Ala) rs192282380
NM_033100.4(CDHR1):c.526-7C>G rs190906755
NM_033100.4(CDHR1):c.556C>T (p.His186Tyr)
NM_033100.4(CDHR1):c.595G>T (p.Asp199Tyr) rs199671784
NM_033100.4(CDHR1):c.628G>A (p.Val210Met) rs774747506
NM_033100.4(CDHR1):c.689C>T (p.Thr230Ile) rs141173656
NM_033100.4(CDHR1):c.783G>A (p.Pro261=) rs147346345
NM_033100.4(CDHR1):c.833C>T (p.Pro278Leu) rs543254581

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.