ClinVar Miner

List of variants reported as likely benign for cardiovascular neoplasm

Included ClinVar conditions (60):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002253.4(KDR):c.1444T>C (p.Cys482Arg) rs34231037 0.02299
NM_000546.6(TP53):c.97-6C>T rs35117667 0.00847
NM_002734.5(PRKAR1A):c.204G>A (p.Leu68=) rs74863634 0.00405
NM_032208.3(ANTXR1):c.1553C>T (p.Ala518Val) rs139807657 0.00253
NM_033360.4(KRAS):c.5-18A>G rs200189105 0.00100
NM_000546.5(TP53):c.319T>C (p.Tyr107His) rs368771578 0.00028
NM_004985.5(KRAS):c.24A>G (p.Val8=) rs147406419 0.00025
NM_000546.6(TP53):c.672+18G>C rs199578278 0.00014
NM_002734.5(PRKAR1A):c.156A>G (p.Glu52=) rs141432364 0.00012
NM_002734.5(PRKAR1A):c.381T>C (p.Ala127=) rs372669687 0.00011
NM_033360.4(KRAS):c.90C>T (p.Asp30=) rs113623140 0.00011
NM_000546.6(TP53):c.847C>T (p.Arg283Cys) rs149633775 0.00009
NM_002734.5(PRKAR1A):c.502+12_502+13del rs764075585 0.00009
NM_033360.4(KRAS):c.4+5G>A rs201789109 0.00006
NM_004985.5(KRAS):c.451-5652C>T rs727505314 0.00004
NM_000546.6(TP53):c.-12C>T rs375229869 0.00002
NM_133171.5(ELMO2):c.1416+9C>G rs770529533 0.00002
NM_002734.5(PRKAR1A):c.549+10A>C rs751413552 0.00001
NM_002734.5(PRKAR1A):c.503-13dup rs138285568
NM_004985.5(KRAS):c.112-9C>T rs727504298
NM_133171.5(ELMO2):c.1279+19del rs76979752

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.