ClinVar Miner

List of variants in gene KRAS reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004985.5(KRAS):c.451-5535A>C rs201170656 0.00019
NM_004985.5(KRAS):c.451-5518T>C rs752925099 0.00004
NM_004985.5(KRAS):c.491G>A (p.Arg164Gln) rs372793780 0.00002
NM_033360.4(KRAS):c.389C>T (p.Ala130Val) rs730880473 0.00002
NM_004985.5(KRAS):c.112-12C>T rs202104024 0.00001
NM_004985.5(KRAS):c.149C>T (p.Thr50Ile) rs1407509439 0.00001
NM_004985.5(KRAS):c.407G>A (p.Ser136Asn) rs757816355 0.00001
NM_004985.5(KRAS):c.451-5538A>G rs755967833 0.00001
NM_033360.4(KRAS):c.*4+1G>A rs780979221 0.00001
NM_033360.4(KRAS):c.491G>A (p.Arg164Gln) rs758575947 0.00001
NM_004985.5(KRAS):c.112-9C>T rs727504298
NM_004985.5(KRAS):c.179G>A (p.Gly60Asp)
NM_004985.5(KRAS):c.180T>A (p.Gly60=) rs397517037
NM_004985.5(KRAS):c.220A>C (p.Thr74Pro) rs770020203
NM_004985.5(KRAS):c.228G>A (p.Glu76=) rs727503107
NM_004985.5(KRAS):c.291-10del rs727503991
NM_004985.5(KRAS):c.470A>G (p.Tyr157Cys) rs794727720
NM_004985.5(KRAS):c.508A>T (p.Met170Leu) rs369501492
NM_033360.4(KRAS):c.140A>G (p.Asp47Gly) rs1565885006
NM_033360.4(KRAS):c.189G>T (p.Glu63Asp) rs1592808357
NM_033360.4(KRAS):c.261del (p.Lys88fs) rs397517038
NM_033360.4(KRAS):c.291-5C>G rs1565884303
NM_033360.4(KRAS):c.400G>A (p.Ala134Thr) rs1565884227
NM_033360.4(KRAS):c.461A>T (p.Asp154Val)

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.