ClinVar Miner

List of variants in gene CCDC40 reported as benign by PreventionGenetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
Download table as spreadsheet
HGVS dbSNP
NM_017950.3(CCDC40):c.-36C>T rs73437681
NM_017950.3(CCDC40):c.-49C>A rs3752042
NM_017950.4(CCDC40):c.1123A>C (p.Lys375Gln) rs61734951
NM_017950.4(CCDC40):c.1131C>T (p.Cys377=) rs74692882
NM_017950.4(CCDC40):c.1132G>A (p.Ala378Thr) rs116795025
NM_017950.4(CCDC40):c.1159+12C>T rs2289533
NM_017950.4(CCDC40):c.1220T>C (p.Ile407Thr) rs141185078
NM_017950.4(CCDC40):c.1303G>A (p.Glu435Lys) rs62000409
NM_017950.4(CCDC40):c.1338C>T (p.Leu446=) rs61734950
NM_017950.4(CCDC40):c.1441-18C>G rs181295177
NM_017950.4(CCDC40):c.1449C>T (p.Thr483=) rs116824266
NM_017950.4(CCDC40):c.1466G>T (p.Ser489Ile) rs61739354
NM_017950.4(CCDC40):c.1531G>A (p.Glu511Lys) rs59978698
NM_017950.4(CCDC40):c.1562+33G>A rs10083858
NM_017950.4(CCDC40):c.1889C>T (p.Ala630Val) rs61749058
NM_017950.4(CCDC40):c.1889_1890delinsTG (p.Ala630Val) rs386799737
NM_017950.4(CCDC40):c.1890T>G (p.Ala630=) rs35578653
NM_017950.4(CCDC40):c.207G>C (p.Val69=) rs2289527
NM_017950.4(CCDC40):c.2255T>C (p.Leu752Pro) rs117203086
NM_017950.4(CCDC40):c.2323G>A (p.Val775Met) rs60684213
NM_017950.4(CCDC40):c.2336G>A (p.Arg779His) rs183809462
NM_017950.4(CCDC40):c.2604C>T (p.Phe868=) rs61749027
NM_017950.4(CCDC40):c.2608C>T (p.Arg870Cys) rs61749025
NM_017950.4(CCDC40):c.2619+25G>A rs151335066
NM_017950.4(CCDC40):c.2682G>A (p.Ala894=) rs4889815
NM_017950.4(CCDC40):c.2784C>T (p.Ile928=) rs118143944
NM_017950.4(CCDC40):c.2832+20G>A rs78493584
NM_017950.4(CCDC40):c.2868G>A (p.Lys956=) rs1982243
NM_017950.4(CCDC40):c.2900G>A (p.Arg967His) rs61686936
NM_017950.4(CCDC40):c.2900G>T (p.Arg967Leu) rs61686936
NM_017950.4(CCDC40):c.3022-28G>A rs74000392
NM_017950.4(CCDC40):c.3022-48C>T rs72849388
NM_017950.4(CCDC40):c.3180+45A>G rs59252872
NM_017950.4(CCDC40):c.504G>A (p.Pro168=) rs74000351
NM_017950.4(CCDC40):c.507G>A (p.Ser169=) rs2885349
NM_017950.4(CCDC40):c.553-17G>C rs7223400
NM_017950.4(CCDC40):c.553-41A>G rs7207441
NM_017950.4(CCDC40):c.630C>T (p.Ser210=) rs117419007
NM_017950.4(CCDC40):c.676+13T>C rs7212525
NM_017950.4(CCDC40):c.677-4C>G rs2289530
NM_017950.4(CCDC40):c.873C>T (p.Phe291=) rs2289531
NM_017950.4(CCDC40):c.93+18C>A rs8074956
NM_017950.4(CCDC40):c.946G>A (p.Ala316Thr) rs61998241

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.