ClinVar Miner

List of variants in gene NRAS reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_002524.5(NRAS):c.291-260C>G rs7549358 0.76128
NM_002524.5(NRAS):c.112-70C>T rs969273 0.76024
NM_002524.5(NRAS):c.451-44G>A rs9724641 0.05260
NM_002524.5(NRAS):c.451-334G>A rs9724640 0.05255
NM_002524.5(NRAS):c.451-200C>T rs61758221 0.02708
NM_002524.4(NRAS):c.-208T>A rs2273267 0.01703
NM_002524.5(NRAS):c.-18+195C>T rs9724618 0.01571
NM_002524.5(NRAS):c.291-315A>G rs181673934 0.00459
NM_002524.5(NRAS):c.43+20G>A rs180892917 0.00158
NM_002524.5(NRAS):c.225C>T (p.Gly75=) rs142739534 0.00123
NM_002524.5(NRAS):c.290+7G>A rs375788140 0.00042
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.112-24C>A rs371806603 0.00007
NM_002524.5(NRAS):c.36T>G (p.Gly12=) rs759764705 0.00006
NM_002524.5(NRAS):c.291-8G>A rs376187980 0.00004
NM_002524.5(NRAS):c.*5A>G rs909455480 0.00003
NM_002524.5(NRAS):c.553C>T (p.Pro185Ser) rs374061873 0.00003
NM_002524.5(NRAS):c.562G>A (p.Val188Met) rs730880381 0.00003
NM_002524.5(NRAS):c.393C>T (p.His131=) rs745954671 0.00002
NM_002524.5(NRAS):c.-16T>C rs1057520403 0.00001
NM_002524.5(NRAS):c.-17-4A>G rs750039795 0.00001
NM_002524.5(NRAS):c.112-6C>G rs200604652 0.00001
NM_002524.5(NRAS):c.147A>C (p.Glu49Asp) rs1370520807 0.00001
NM_002524.5(NRAS):c.159G>A (p.Leu53=) rs114668710 0.00001
NM_002524.5(NRAS):c.179G>A (p.Gly60Glu) rs267606920 0.00001
NM_002524.5(NRAS):c.250A>G (p.Ile84Val) rs376177995 0.00001
NM_002524.5(NRAS):c.315C>T (p.Asp105=) rs752000303 0.00001
NM_002524.5(NRAS):c.325G>C (p.Val109Leu) rs730880966 0.00001
NM_002524.5(NRAS):c.35G>A (p.Gly12Asp) rs121913237 0.00001
NM_002524.5(NRAS):c.432C>T (p.Thr144=) rs753079400 0.00001
NM_002524.5(NRAS):c.450+18G>T rs766994734 0.00001
NM_002524.5(NRAS):c.464C>T (p.Ala155Val) rs747080102 0.00001
NM_002524.5(NRAS):c.504G>C (p.Met168Ile) rs367918552 0.00001
NM_002524.5(NRAS):c.69A>G (p.Leu23=) rs771113899 0.00001
NM_002524.5(NRAS):c.87A>G (p.Val29=) rs748537067 0.00001
NM_002524.5(NRAS):c.112-1_113dup rs730880967
NM_002524.5(NRAS):c.112-24dup rs780595451
NM_002524.5(NRAS):c.112-3del rs1064794197
NM_002524.5(NRAS):c.173C>T (p.Thr58Ile) rs2101742052
NM_002524.5(NRAS):c.175G>A (p.Ala59Thr) rs730880965
NM_002524.5(NRAS):c.178G>A (p.Gly60Arg) rs1557982817
NM_002524.5(NRAS):c.182A>C (p.Gln61Pro) rs11554290
NM_002524.5(NRAS):c.182A>G (p.Gln61Arg) rs11554290
NM_002524.5(NRAS):c.183A>T (p.Gln61His) rs121913255
NM_002524.5(NRAS):c.259A>T (p.Ser87Cys)
NM_002524.5(NRAS):c.260G>A (p.Ser87Asn) rs1385254281
NM_002524.5(NRAS):c.268T>C (p.Phe90Leu) rs1393160852
NM_002524.5(NRAS):c.272C>T (p.Ala91Val) rs774832953
NM_002524.5(NRAS):c.290+15A>C rs373417606
NM_002524.5(NRAS):c.304C>T (p.Arg102Ter)
NM_002524.5(NRAS):c.305G>A (p.Arg102Gln)
NM_002524.5(NRAS):c.317C>T (p.Ser106Leu) rs797045795
NM_002524.5(NRAS):c.31G>A (p.Ala11Thr) rs1367788342
NM_002524.5(NRAS):c.334G>T (p.Val112Leu) rs730880968
NM_002524.5(NRAS):c.34G>A (p.Gly12Ser) rs121913250
NM_002524.5(NRAS):c.34G>C (p.Gly12Arg) rs121913250
NM_002524.5(NRAS):c.34G>T (p.Gly12Cys) rs121913250
NM_002524.5(NRAS):c.35G>C (p.Gly12Ala) rs121913237
NM_002524.5(NRAS):c.35G>T (p.Gly12Val) rs121913237
NM_002524.5(NRAS):c.368G>A (p.Arg123Lys) rs727503347
NM_002524.5(NRAS):c.370A>G (p.Thr124Ala) rs747732620
NM_002524.5(NRAS):c.371C>T (p.Thr124Ile)
NM_002524.5(NRAS):c.38G>A (p.Gly13Asp) rs121434596
NM_002524.5(NRAS):c.394G>C (p.Glu132Gln) rs1456325880
NM_002524.5(NRAS):c.442A>G (p.Thr148Ala) rs730880969
NM_002524.5(NRAS):c.451-21_451-19del rs754048062
NM_002524.5(NRAS):c.478G>A (p.Val160Ile) rs2101737856
NM_002524.5(NRAS):c.525T>C (p.Asp175=) rs1057524394
NM_002524.5(NRAS):c.542G>T (p.Cys181Phe) rs2101737803
NM_002524.5(NRAS):c.554C>T (p.Pro185Leu) rs2101737789
NM_002524.5(NRAS):c.565A>G (p.Met189Val) rs1557980814
NM_002524.5(NRAS):c.64C>T (p.Gln22Ter) rs1178238823
NM_002524.5(NRAS):c.71T>A (p.Ile24Asn) rs869025573
NM_002524.5(NRAS):c.74A>G (p.Gln25Arg) rs2101744093

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