ClinVar Miner

List of variants in gene combination CDK4, TSPAN31 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005981.5(TSPAN31):c.*2414A>T rs3211619 0.01284
NM_005981.5(TSPAN31):c.*2372T>C rs3211620 0.01221
NM_005981.5(TSPAN31):c.*1551G>C rs3211628 0.00693
NM_005981.5(TSPAN31):c.*2429C>T rs73338241 0.00348
NM_000075.4(CDK4):c.764G>A (p.Arg255His) rs144657355 0.00037
NM_005981.5(TSPAN31):c.*2031T>A rs370609910 0.00016
NM_000075.4(CDK4):c.834T>C (p.Phe278=) rs115576923 0.00013
NM_000075.4(CDK4):c.702A>C (p.Pro234=) rs368081942 0.00006
NM_005981.5(TSPAN31):c.*1881A>G rs188641164 0.00002
NM_000075.4(CDK4):c.660C>T (p.Ala220=) rs773490152 0.00001
NM_005981.5(TSPAN31):c.*1421T>C rs2069509 0.00001
NM_005981.5(TSPAN31):c.*2032G>A rs765361338 0.00001
NM_005981.5(TSPAN31):c.*2037dup rs757684130 0.00001
NM_000075.4(CDK4):c.651C>T (p.Asn217=) rs876659462
NM_000075.4(CDK4):c.705G>A (p.Glu235=) rs374223296
NM_000075.4(CDK4):c.762C>T (p.Pro254=) rs753908111
NM_005981.5(TSPAN31):c.*1223C>G rs770044583
NM_005981.5(TSPAN31):c.*1578G>C rs144984374
NM_005981.5(TSPAN31):c.*1658C>T rs3211626
NM_005981.5(TSPAN31):c.*2156T>A rs1446831422

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.