ClinVar Miner

List of variants in gene CBL, MCAM studied for Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 57
Download table as spreadsheet
HGVS dbSNP
NM_005188.3(CBL):c.*5986T>C rs764329156
NM_005188.3(CBL):c.*5987A>T rs150688966
NM_005188.3(CBL):c.*6008T>C rs3829261
NM_005188.3(CBL):c.*6099A>G rs575606651
NM_005188.3(CBL):c.*6126T>A rs886047803
NM_005188.3(CBL):c.*6175A>G rs775450592
NM_005188.3(CBL):c.*6265C>A rs886047804
NM_005188.3(CBL):c.*6362G>A rs886047805
NM_005188.3(CBL):c.*6430G>C rs886047806
NM_005188.3(CBL):c.*6542T>G rs550863116
NM_005188.3(CBL):c.*6575G>C rs569180524
NM_005188.3(CBL):c.*6648T>G rs544221090
NM_005188.3(CBL):c.*6703T>C rs562568416
NM_005188.3(CBL):c.*6732C>A rs140028176
NM_005188.3(CBL):c.*6767C>G rs539341635
NM_005188.3(CBL):c.*6933C>A rs886047807
NM_005188.3(CBL):c.*6980T>C rs886047808
NM_005188.3(CBL):c.*7081T>G rs886047809
NM_005188.3(CBL):c.*7143A>C rs146650854
NM_005188.3(CBL):c.*7167A>C rs886047812
NM_005188.3(CBL):c.*7314T>C rs144022588
NM_005188.3(CBL):c.*7366C>T rs534426893
NM_005188.3(CBL):c.*7447A>G rs11217234
NM_005188.3(CBL):c.*7559C>G rs1052121
NM_005188.3(CBL):c.*7659C>A rs567049953
NM_005188.3(CBL):c.*7659C>G rs567049953
NM_005188.3(CBL):c.*7689C>G rs187961956
NM_005188.3(CBL):c.*7761G>A rs745412309
NM_005188.3(CBL):c.*7903G>A rs201889676
NM_005188.3(CBL):c.*7904G>A rs886047813
NM_005188.3(CBL):c.*7949C>A rs142183037
NM_005188.3(CBL):c.*7978A>G rs2511836
NM_005188.3(CBL):c.*8012T>C rs573686690
NM_005188.3(CBL):c.*8017G>A rs533150203
NM_005188.3(CBL):c.*8048G>A rs151221935
NM_005188.3(CBL):c.*8058C>T rs569107221
NM_005188.3(CBL):c.*8149A>G rs11243
NM_005188.4(CBL):c.*6261A>T
NM_005188.4(CBL):c.*6429T>C
NM_005188.4(CBL):c.*6484G>A
NM_005188.4(CBL):c.*6528T>C
NM_005188.4(CBL):c.*6532A>G
NM_005188.4(CBL):c.*6678G>A
NM_005188.4(CBL):c.*6712C>G
NM_005188.4(CBL):c.*6729C>T
NM_005188.4(CBL):c.*6795A>G
NM_005188.4(CBL):c.*6806T>C
NM_005188.4(CBL):c.*6872A>T
NM_005188.4(CBL):c.*7030T>G
NM_005188.4(CBL):c.*7241A>G
NM_005188.4(CBL):c.*7601G>A
NM_005188.4(CBL):c.*7659C>T
NM_005188.4(CBL):c.*7678G>A
NM_005188.4(CBL):c.*7855C>T
NM_005188.4(CBL):c.*7878C>T
NM_005188.4(CBL):c.*7924C>A
NM_005188.4(CBL):c.*8318C>T

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.