ClinVar Miner

List of variants in gene NRAS reported as uncertain significance for Noonan syndrome 6

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002524.5(NRAS):c.*2523A>G rs143441947 0.00163
NM_002524.5(NRAS):c.*3404T>C rs185234485 0.00145
NM_002524.5(NRAS):c.*2805T>C rs776606789 0.00100
NM_002524.5(NRAS):c.*2513T>A rs150969241 0.00091
NM_002524.5(NRAS):c.*2618A>G rs528439389 0.00058
NM_002524.5(NRAS):c.360G>A (p.Leu120=) rs143020946 0.00034
NM_002524.5(NRAS):c.112-8A>G rs9724626 0.00025
NM_002524.5(NRAS):c.*2844T>A rs530053161 0.00022
NM_002524.5(NRAS):c.*111A>G rs188272768 0.00019
NM_002524.5(NRAS):c.*344A>G rs746680042 0.00014
NM_002524.5(NRAS):c.*2546C>T rs778203603 0.00013
NM_002524.5(NRAS):c.*2630G>A rs886045102 0.00009
NM_002524.5(NRAS):c.*2767C>T rs766572336 0.00006
NM_002524.5(NRAS):c.*651C>T rs754089086 0.00006
NM_002524.5(NRAS):c.*3062C>T rs886045098 0.00005
NM_002524.5(NRAS):c.*1629C>G rs776223586 0.00004
NM_002524.5(NRAS):c.553C>T (p.Pro185Ser) rs374061873 0.00003
NM_002524.5(NRAS):c.*1509A>G rs141713248 0.00002
NM_002524.5(NRAS):c.*1914A>G rs967317719 0.00002
NM_002524.5(NRAS):c.*1466A>T rs374183050 0.00001
NM_002524.5(NRAS):c.*1571A>G rs1457248724 0.00001
NM_002524.5(NRAS):c.*1974T>C rs1658914654 0.00001
NM_002524.5(NRAS):c.*2188C>A rs1249096456 0.00001
NM_002524.5(NRAS):c.*3103G>T rs1290377688 0.00001
NM_002524.5(NRAS):c.*3341A>T rs1658865519 0.00001
NM_002524.5(NRAS):c.*340G>A rs1176222040 0.00001
NM_002524.5(NRAS):c.*536C>T rs886045108 0.00001
NM_002524.5(NRAS):c.*774A>G rs886045107 0.00001
NM_002524.5(NRAS):c.112-6C>G rs200604652 0.00001
NM_002524.5(NRAS):c.250A>G (p.Ile84Val) rs376177995 0.00001
NM_002524.5(NRAS):c.*1105C>T rs1658933470
NM_002524.5(NRAS):c.*1382G>T rs886045105
NM_002524.5(NRAS):c.*1643G>C rs571329214
NM_002524.5(NRAS):c.*1656C>T rs886045104
NM_002524.5(NRAS):c.*1845T>C rs1480696185
NM_002524.5(NRAS):c.*1887T>C rs1658917145
NM_002524.5(NRAS):c.*1936C>G rs1658915425
NM_002524.5(NRAS):c.*2178G>A rs886045103
NM_002524.5(NRAS):c.*2226G>C rs1658900816
NM_002524.5(NRAS):c.*2328G>A rs1201037392
NM_002524.5(NRAS):c.*2412G>A rs757692247
NM_002524.5(NRAS):c.*2589G>A rs556142436
NM_002524.5(NRAS):c.*2677A>T rs886045101
NM_002524.5(NRAS):c.*2714G>T rs886045100
NM_002524.5(NRAS):c.*2811C>A rs1658883840
NM_002524.5(NRAS):c.*2860G>A rs886045099
NM_002524.5(NRAS):c.*3020A>G rs550638204
NM_002524.5(NRAS):c.*3362T>C rs577115849
NM_002524.5(NRAS):c.*3392T>C rs886045097
NM_002524.5(NRAS):c.*3430T>A rs539638523
NM_002524.5(NRAS):c.380C>G (p.Thr127Arg) rs779899354

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.