ClinVar Miner

List of variants in gene CDKN2A reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_058195.4(CDKN2A):c.194-4112A>T rs36228834 0.02003
NM_000077.5(CDKN2A):c.150+1277G>A rs72547290 0.01241
NM_000077.5(CDKN2A):c.150+216_150+218del rs201820199 0.01056
NM_000077.5(CDKN2A):c.150+365T>G rs115521447 0.01050
NM_000077.5(CDKN2A):c.150+221_150+226del rs200504822 0.00895
NM_000077.5(CDKN2A):c.150+1306C>G rs76709929 0.00641
NM_058195.4(CDKN2A):c.194-3799G>A rs145660371 0.00600
NM_000077.5(CDKN2A):c.151-1238G>A rs3731245 0.00519
NM_000077.5(CDKN2A):c.457+227A>G rs113886003 0.00516
NM_000077.5(CDKN2A):c.151-145T>C rs3731247 0.00475
NM_000077.5(CDKN2A):c.151-223G>A rs138233963 0.00397
NM_000077.5(CDKN2A):c.174A>C (p.Arg58=) rs201208890 0.00273
NM_000077.5(CDKN2A):c.458-491C>T rs181044510 0.00229
NM_000077.5(CDKN2A):c.150+37G>C rs45456595 0.00212
NM_058195.4(CDKN2A):c.-28C>G rs149253558 0.00035
NM_000077.5(CDKN2A):c.51C>A (p.Ala17=) rs764362225 0.00019
NM_000077.5(CDKN2A):c.87G>A (p.Arg29=) rs540871544 0.00009
NM_000077.5(CDKN2A):c.197A>G (p.His66Arg) rs756750256 0.00004
NM_000077.5(CDKN2A):c.405G>A (p.Gly135=) rs751586391 0.00004
NM_000077.5(CDKN2A):c.147C>A (p.Ile49=) rs200738474 0.00003
NM_000077.5(CDKN2A):c.151-13T>C rs757122222 0.00003
NM_000077.5(CDKN2A):c.*6C>G rs375628411 0.00002
NM_058195.4(CDKN2A):c.92C>G (p.Thr31Arg) rs528789830 0.00002
NM_000077.5(CDKN2A):c.396G>C (p.Ala132=) rs745702441 0.00001
NM_000077.5(CDKN2A):c.458-10C>G rs748219065 0.00001
NM_000077.5(CDKN2A):c.468T>C (p.Asp156=) rs749753811 0.00001
NM_000077.5(CDKN2A):c.57C>T (p.Ala19=) rs1060504186 0.00001
NM_058195.4(CDKN2A):c.-22C>T rs1460467871 0.00001
NM_058195.4(CDKN2A):c.-2A>T rs764949869 0.00001
NM_058195.4(CDKN2A):c.-42G>C rs755734889 0.00001
NM_058195.4(CDKN2A):c.135C>G (p.Leu45=) rs766676234 0.00001
NM_058195.4(CDKN2A):c.36G>T (p.Arg12=) rs1305455942 0.00001
NM_000077.5(CDKN2A):c.*8A>G rs763795863
NM_000077.5(CDKN2A):c.*8A>T rs763795863
NM_000077.5(CDKN2A):c.150+12G>A rs1057520264
NM_000077.5(CDKN2A):c.150+18A>G rs1251604295
NM_000077.5(CDKN2A):c.150+20C>G rs550846229
NM_000077.5(CDKN2A):c.150+8G>A rs1419306566
NM_000077.5(CDKN2A):c.151-117_151-114del rs527380593
NM_000077.5(CDKN2A):c.151-18_151-13delinsCTCTGC rs1064794613
NM_000077.5(CDKN2A):c.151-7C>G rs1482685317
NM_000077.5(CDKN2A):c.360G>A (p.Glu120=) rs757308315
NM_000077.5(CDKN2A):c.369T>A (p.His123Gln) rs6413463
NM_000077.5(CDKN2A):c.369T>C (p.His123=) rs6413463
NM_000077.5(CDKN2A):c.441C>A (p.Ala147=) rs1057524065
NM_000077.5(CDKN2A):c.457+11A>G rs1057521424
NM_000077.5(CDKN2A):c.458-15T>A rs772321849
NM_000077.5(CDKN2A):c.458-4G>C rs876660514
NM_000077.5(CDKN2A):c.462C>A (p.Ile154=) rs1554653281
NM_000077.5(CDKN2A):c.54G>T (p.Thr18=) rs765702324
NM_000077.5(CDKN2A):c.66G>A (p.Arg22=) rs776810546
NM_000077.5(CDKN2A):c.72G>T (p.Arg24=) rs1449870708
NM_058195.4(CDKN2A):c.-46G>A rs779168896
NM_058195.4(CDKN2A):c.-6G>A rs1057521467
NM_058195.4(CDKN2A):c.16T>C (p.Leu6=) rs1554659245
NM_058195.4(CDKN2A):c.30G>A (p.Arg10=) rs876658436
NM_058195.4(CDKN2A):c.30G>T (p.Arg10=) rs876658436
NM_058195.4(CDKN2A):c.48C>T (p.Gly16=) rs786202556
NM_058195.4(CDKN2A):c.75T>C (p.Val25=) rs1057522328

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