ClinVar Miner

List of variants in gene NRAS studied for Noonan syndrome

Included ClinVar conditions (23):
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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP
NM_002524.3(NRAS):c.35G>T (p.Gly12Val) rs121913237
NM_002524.3(NRAS):c.38G>A (p.Gly13Asp) rs121434596
NM_002524.4(NRAS):c.*1062_*1063delTT rs775070295
NM_002524.4(NRAS):c.*111A>G rs188272768
NM_002524.4(NRAS):c.*1382G>T rs886045105
NM_002524.4(NRAS):c.*1643G>C rs571329214
NM_002524.4(NRAS):c.*1656C>T rs886045104
NM_002524.4(NRAS):c.*2178G>A rs886045103
NM_002524.4(NRAS):c.*2327C>T rs533027827
NM_002524.4(NRAS):c.*2464A>G rs140878667
NM_002524.4(NRAS):c.*2510_*2515delTAGTTA rs549171175
NM_002524.4(NRAS):c.*2513T>A rs150969241
NM_002524.4(NRAS):c.*2546C>T rs778203603
NM_002524.4(NRAS):c.*2630G>A rs886045102
NM_002524.4(NRAS):c.*2662G>A rs148827219
NM_002524.4(NRAS):c.*2667T>C rs145382662
NM_002524.4(NRAS):c.*2677A>T rs886045101
NM_002524.4(NRAS):c.*2714G>T rs886045100
NM_002524.4(NRAS):c.*2784T>A rs374889066
NM_002524.4(NRAS):c.*2805T>C rs776606789
NM_002524.4(NRAS):c.*2844T>A rs530053161
NM_002524.4(NRAS):c.*2860G>A rs886045099
NM_002524.4(NRAS):c.*2965delT rs61652108
NM_002524.4(NRAS):c.*3062C>T rs886045098
NM_002524.4(NRAS):c.*3219C>G rs72994441
NM_002524.4(NRAS):c.*3366G>T rs72994440
NM_002524.4(NRAS):c.*3384C>T rs140049110
NM_002524.4(NRAS):c.*3392T>C rs886045097
NM_002524.4(NRAS):c.*3404T>C rs185234485
NM_002524.4(NRAS):c.*344A>G rs746680042
NM_002524.4(NRAS):c.*346G>A rs9724642
NM_002524.4(NRAS):c.*3499C>T rs147926293
NM_002524.4(NRAS):c.*416A>C rs9724643
NM_002524.4(NRAS):c.*536C>T rs886045108
NM_002524.4(NRAS):c.*583T>G rs555171083
NM_002524.4(NRAS):c.*740G>A rs372008962
NM_002524.4(NRAS):c.*774A>G rs886045107
NM_002524.4(NRAS):c.*872C>T rs14804
NM_002524.4(NRAS):c.*935dupA rs886045106
NM_002524.4(NRAS):c.-106G>T rs755583487
NM_002524.4(NRAS):c.-132C>T rs886045109
NM_002524.4(NRAS):c.-179G>C rs886045110
NM_002524.4(NRAS):c.-208T>A rs2273267
NM_002524.4(NRAS):c.-209A>G rs886045111
NM_002524.4(NRAS):c.-242G>C rs886045112
NM_002524.4(NRAS):c.-245C>T rs886045113
NM_002524.4(NRAS):c.-50A>G rs61758211
NM_002524.4(NRAS):c.101C>T (p.Pro34Leu) rs397514553
NM_002524.4(NRAS):c.149C>T (p.Thr50Ile) rs267606921
NM_002524.4(NRAS):c.179G>A (p.Gly60Glu) rs267606920
NM_002524.4(NRAS):c.225C>T (p.Gly75=) rs142739534
NM_002524.4(NRAS):c.317C>T (p.Ser106Leu) rs797045795
NM_002524.4(NRAS):c.380C>G (p.Thr127Arg) rs779899354
NM_002524.4(NRAS):c.553C>T (p.Pro185Ser) rs374061873
NM_002524.4(NRAS):c.71T>A (p.Ile24Asn) rs869025573

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