ClinVar Miner

List of variants in gene KRAS reported as likely benign for Noonan syndrome

Included ClinVar conditions (23):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
Download table as spreadsheet
HGVS dbSNP
NM_004985.4(KRAS):c.*1062G>A rs61763591
NM_004985.4(KRAS):c.*1083A>G rs7960917
NM_004985.4(KRAS):c.*1418_*1420delAAA rs200038818
NM_004985.4(KRAS):c.*1540T>C rs61764366
NM_004985.4(KRAS):c.*1587T>C rs7973450
NM_004985.4(KRAS):c.*1627dup rs71065923
NM_004985.4(KRAS):c.*1637_*1638delTA rs535478558
NM_004985.4(KRAS):c.*1638A>G rs4597149
NM_004985.4(KRAS):c.*1655C>T rs7973623
NM_004985.4(KRAS):c.*1765T>C rs115968671
NM_004985.4(KRAS):c.*177T>G rs712
NM_004985.4(KRAS):c.*2184A>G rs61764368
NM_004985.4(KRAS):c.*2279dup rs56128001
NM_004985.4(KRAS):c.*2371C>T rs61764369
NM_004985.4(KRAS):c.*2505T>G rs61764370
NM_004985.4(KRAS):c.*2888A>G rs13096
NM_004985.4(KRAS):c.*3152G>A rs61764371
NM_004985.4(KRAS):c.*3264delT rs34176876
NM_004985.4(KRAS):c.*3377C>T rs1137188
NM_004985.4(KRAS):c.*3401T>A rs1137189
NM_004985.4(KRAS):c.*3502T>A rs61764372
NM_004985.4(KRAS):c.*3683dup rs142323886
NM_004985.4(KRAS):c.*3760A>C rs1137196
NM_004985.4(KRAS):c.*3786A>G rs8720
NM_004985.4(KRAS):c.*3901A>C rs12587
NM_004985.4(KRAS):c.*404T>C rs140080026
NM_004985.4(KRAS):c.*4065_*4066delAA rs34719539
NM_004985.4(KRAS):c.*4079T>A rs12245
NM_004985.4(KRAS):c.*4305_*4306dup rs61764373
NM_004985.4(KRAS):c.*4311A>G rs61764374
NM_004985.4(KRAS):c.*512T>C rs9266
NM_004985.4(KRAS):c.*824T>C rs61763589
NM_004985.4(KRAS):c.*973G>T rs61763590
NM_004985.4(KRAS):c.451-9G>A rs12313763
NM_004985.4(KRAS):c.490C>T (p.Arg164Ter) rs1555192443
NM_004985.4(KRAS):c.519T>C (p.Asp173=) rs1137282

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.