ClinVar Miner

List of variants in gene CNTN1 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001843.4(CNTN1):c.1893T>C (p.His631=) rs2229929 0.03763
NM_001843.4(CNTN1):c.401-9C>T rs57340925 0.02401
NM_001843.4(CNTN1):c.2324G>A (p.Ser775Asn) rs34326474 0.00980
NM_001843.4(CNTN1):c.2670A>T (p.Gly890=) rs34346038 0.00972
NM_001843.4(CNTN1):c.207C>T (p.Ala69=) rs7297132 0.00583
NM_001843.4(CNTN1):c.2493T>C (p.His831=) rs61754102 0.00396
NM_001843.4(CNTN1):c.497-17G>T rs142799954 0.00276
NM_001843.4(CNTN1):c.2598C>G (p.Ala866=) rs140462332 0.00120
NM_001843.4(CNTN1):c.804-8A>G rs56172264 0.00106
NM_001843.4(CNTN1):c.400+13T>C rs201396853 0.00105
NM_001843.4(CNTN1):c.1507+19G>T rs145594554 0.00099
NM_001843.4(CNTN1):c.2824-6T>C rs201098244 0.00010
NM_001843.4(CNTN1):c.2114-20T>C rs896908779 0.00004
NM_001843.4(CNTN1):c.2553A>G (p.Glu851=) rs150210369 0.00004
NM_001843.4(CNTN1):c.2100A>G (p.Lys700=) rs1555195505
NM_001843.4(CNTN1):c.2114-17T>G rs1555199184
NM_001843.4(CNTN1):c.2178A>G (p.Thr726=) rs1291165164
NM_001843.4(CNTN1):c.2185-11T>C rs1555199578
NM_001843.4(CNTN1):c.2694T>C (p.Ala898=) rs1555200914
NM_001843.4(CNTN1):c.342T>C (p.Cys114=) rs1555180947
NM_001843.4(CNTN1):c.401-14del rs148387796
NM_001843.4(CNTN1):c.905T>C (p.Leu302Pro) rs548330075
NM_001843.4(CNTN1):c.985+20T>A rs1057523160

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.