ClinVar Miner

List of variants in gene RRAS reported as uncertain significance for RASopathy

Included ClinVar conditions (37):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_006270.4(RRAS):c.145T>C (p.Phe49Leu) rs151014532
NM_006270.4(RRAS):c.158A>T (p.Tyr53Phe)
NM_006270.4(RRAS):c.167C>G (p.Ser56Cys)
NM_006270.4(RRAS):c.175G>C (p.Asp59His)
NM_006270.4(RRAS):c.338G>A (p.Arg113Gln)
NM_006270.4(RRAS):c.371C>T (p.Thr124Met) rs369508242
NM_006270.4(RRAS):c.400G>A (p.Asp134Asn)
NM_006270.4(RRAS):c.409G>A (p.Val137Ile) rs757080959
NM_006270.4(RRAS):c.454-6C>T
NM_006270.4(RRAS):c.472_473insTT (p.Ser158Phefs)
NM_006270.4(RRAS):c.49G>T (p.Gly17Trp)
NM_006270.4(RRAS):c.515C>T (p.Ser172Leu) rs754342165
NM_006270.4(RRAS):c.623A>G (p.Lys208Arg)
NM_006270.4(RRAS):c.631G>A (p.Gly211Arg)
NM_006270.4(RRAS):c.649C>G (p.Leu217Val)
NM_006270.4(RRAS):c.64G>T (p.Gly22Trp) rs754976061

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.