ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006270.5(RRAS):c.568G>C (p.Val190Leu) rs2230917 0.00128
NM_006270.5(RRAS):c.362A>G (p.Lys121Arg) rs138124318 0.00121
NM_006270.5(RRAS):c.379C>T (p.Leu127=) rs145907892 0.00111
NM_006270.5(RRAS):c.145T>C (p.Phe49Leu) rs151014532 0.00107
NM_006270.5(RRAS):c.573-12G>A rs201690554 0.00086
NM_006270.5(RRAS):c.154-4C>G rs372925843 0.00057
NM_006270.5(RRAS):c.174C>T (p.Tyr58=) rs145282813 0.00055
NM_006270.5(RRAS):c.345-4G>A rs377672475 0.00029
NM_006270.5(RRAS):c.454-9T>C rs1490597941 0.00027
NM_006270.5(RRAS):c.345-19C>G rs369700575 0.00023
NM_006270.5(RRAS):c.516G>C (p.Ser172=) rs199924228 0.00016
NM_006270.5(RRAS):c.255G>A (p.Ala85=) rs142801791 0.00015
NM_006270.5(RRAS):c.600G>A (p.Pro200=) rs183538580 0.00015
NM_006270.5(RRAS):c.81C>T (p.Ser27=) rs375821724 0.00011
NM_006270.5(RRAS):c.540C>T (p.Asp180=) rs781054110 0.00009
NM_006270.5(RRAS):c.344+17G>A rs761080520 0.00008
NM_006270.5(RRAS):c.229G>A (p.Ala77Thr) rs200611081 0.00006
NM_006270.5(RRAS):c.495C>T (p.His165=) rs765681955 0.00005
NM_006270.5(RRAS):c.645C>T (p.Cys215=) rs149038492 0.00005
NM_006270.5(RRAS):c.154-5G>A rs753238136 0.00004
NM_006270.5(RRAS):c.324C>T (p.Phe108=) rs578092373 0.00004
NM_006270.5(RRAS):c.543G>A (p.Glu181=) rs370876982 0.00004
NM_006270.5(RRAS):c.241+9G>A rs750643775 0.00003
NM_006270.5(RRAS):c.291C>T (p.Tyr97=) rs780638908 0.00003
NM_006270.5(RRAS):c.573-13C>T rs372538436 0.00003
NM_006270.5(RRAS):c.573-19C>G rs377060262 0.00003
NM_006270.5(RRAS):c.242-8C>T rs370459010 0.00002
NM_006270.5(RRAS):c.454-19G>A rs776793181 0.00002
NM_006270.5(RRAS):c.572+20T>G rs1017127642 0.00002
NM_006270.5(RRAS):c.94C>T (p.Leu32=) rs764926027 0.00002
NM_006270.5(RRAS):c.102C>T (p.Val34=) rs754204165 0.00001
NM_006270.5(RRAS):c.201G>A (p.Thr67=) rs1421164782 0.00001
NM_006270.5(RRAS):c.241+13A>G rs765391621 0.00001
NM_006270.5(RRAS):c.351C>T (p.Asn117=) rs374077706 0.00001
NM_006270.5(RRAS):c.363G>A (p.Lys121=) rs557007484 0.00001
NM_006270.5(RRAS):c.372G>A (p.Thr124=) rs368978550 0.00001
NM_006270.5(RRAS):c.37C>A (p.Arg13=) rs1272875791 0.00001
NM_006270.5(RRAS):c.396C>T (p.Arg132=) rs748366671 0.00001
NM_006270.5(RRAS):c.534C>T (p.Asn178=) rs773121618 0.00001
NM_006270.5(RRAS):c.624G>A (p.Lys208=) rs775471738 0.00001
NM_006270.5(RRAS):c.652C>T (p.Leu218=) rs781768996 0.00001
NM_006270.5(RRAS):c.69C>T (p.Asp23=) rs1458889244 0.00001
NM_006270.5(RRAS):c.153+10C>A
NM_006270.5(RRAS):c.153+18G>A
NM_006270.5(RRAS):c.154-10A>T
NM_006270.5(RRAS):c.154-6C>T
NM_006270.5(RRAS):c.162C>T (p.Phe54=)
NM_006270.5(RRAS):c.231C>A (p.Ala77=) rs557964716
NM_006270.5(RRAS):c.241+17T>C
NM_006270.5(RRAS):c.241+20A>G
NM_006270.5(RRAS):c.242-12_242-11del
NM_006270.5(RRAS):c.242-8C>G
NM_006270.5(RRAS):c.252C>T (p.Thr84=)
NM_006270.5(RRAS):c.270C>T (p.Phe90=)
NM_006270.5(RRAS):c.288G>A (p.Gln96=)
NM_006270.5(RRAS):c.306C>T (p.His102=)
NM_006270.5(RRAS):c.30G>C (p.Gly10=) rs901769495
NM_006270.5(RRAS):c.345-19_345-18del rs2122419483
NM_006270.5(RRAS):c.345-5C>T
NM_006270.5(RRAS):c.408C>G (p.Pro136=) rs114187560
NM_006270.5(RRAS):c.42C>T (p.Pro14=) rs1354856207
NM_006270.5(RRAS):c.438G>T (p.Leu146=) rs1599813671
NM_006270.5(RRAS):c.43C>A (p.Arg15=) rs544651800
NM_006270.5(RRAS):c.453+17T>C
NM_006270.5(RRAS):c.453+18T>C rs2122418915
NM_006270.5(RRAS):c.453+7G>A rs2122418958
NM_006270.5(RRAS):c.454-11C>G
NM_006270.5(RRAS):c.454-13C>T
NM_006270.5(RRAS):c.454-20C>T
NM_006270.5(RRAS):c.454-4C>T
NM_006270.5(RRAS):c.454-7C>T rs2122417189
NM_006270.5(RRAS):c.454-9T>A rs1490597941
NM_006270.5(RRAS):c.480C>T (p.Phe160=)
NM_006270.5(RRAS):c.492C>T (p.His164=) rs2122416934
NM_006270.5(RRAS):c.516G>A (p.Ser172=) rs199924228
NM_006270.5(RRAS):c.516G>T (p.Ser172=)
NM_006270.5(RRAS):c.567T>C (p.Ala189=)
NM_006270.5(RRAS):c.572+13C>A
NM_006270.5(RRAS):c.573-15G>A
NM_006270.5(RRAS):c.573-16del
NM_006270.5(RRAS):c.609C>T (p.Pro203=)
NM_006270.5(RRAS):c.630C>T (p.Gly210=)
NM_006270.5(RRAS):c.642C>T (p.Pro214=)
NM_006270.5(RRAS):c.66G>A (p.Gly22=) rs1249345635
NM_006270.5(RRAS):c.75G>C (p.Pro25=) rs2122429854

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.