ClinVar Miner

List of variants in gene CDKN2A reported as likely benign for not provided

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_000077.5(CDKN2A):c.442G>A (p.Ala148Thr) rs3731249 0.02007
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+365T>G rs115521447 0.01050
NM_000077.5(CDKN2A):c.150+216_150+218del rs201820199 0.00970
NM_000077.5(CDKN2A):c.150+221_150+226del rs200504822 0.00970
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 0.00507
NM_000077.5(CDKN2A):c.379G>T (p.Ala127Ser) rs6413464 0.00490
NM_000077.5(CDKN2A):c.151-145T>C rs3731247 0.00434
NM_000077.5(CDKN2A):c.151-223G>A rs138233963 0.00370
NM_000077.5(CDKN2A):c.174A>C (p.Arg58=) rs201208890 0.00273
NM_000077.5(CDKN2A):c.150+216A>G rs147602781 0.00257
NM_000077.5(CDKN2A):c.430C>T (p.Arg144Cys) rs116150891 0.00248
NM_000077.5(CDKN2A):c.458-491C>T rs181044510 0.00229
NM_000077.5(CDKN2A):c.150+37G>C rs45456595 0.00212
NR_024274.1(CDKN2A-AS1):n.154T>G rs201859802 0.00198
NM_000077.5(CDKN2A):c.150+280C>T rs150201743 0.00055
NM_058195.4(CDKN2A):c.-28C>G rs149253558 0.00035
NM_000077.5(CDKN2A):c.150+153T>A rs150447516 0.00029
NM_000077.5(CDKN2A):c.318G>A (p.Val106=) rs199888003 0.00026
NM_058195.4(CDKN2A):c.69C>T (p.Phe23=) rs374360796 0.00024
NM_000077.5(CDKN2A):c.51C>A (p.Ala17=) rs764362225 0.00019
NM_000077.5(CDKN2A):c.365G>T (p.Gly122Val) rs373291490 0.00016
NM_000077.5(CDKN2A):c.197A>G (p.His66Arg) rs756750256 0.00009
NM_000077.5(CDKN2A):c.405G>A (p.Gly135=) rs751586391 0.00009
NM_000077.5(CDKN2A):c.87G>A (p.Arg29=) rs540871544 0.00009
NM_000077.5(CDKN2A):c.150+27A>C rs762508111 0.00006
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_000077.5(CDKN2A):c.151-18T>C rs779541481 0.00002
NM_058195.4(CDKN2A):c.135C>G (p.Leu45=) rs766676234 0.00002
NM_058195.4(CDKN2A):c.92C>G (p.Thr31Arg) rs528789830 0.00002
NM_000077.5(CDKN2A):c.225C>G (p.Pro75=) rs762397298 0.00001
NM_000077.5(CDKN2A):c.288G>A (p.Val96=) rs557319056 0.00001
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.36G>T (p.Arg12=) rs1305455942 0.00001
NM_000077.5(CDKN2A):c.*8A>T rs763795863
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.225C>T (p.Pro75=) rs762397298
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.458-56G>T rs1563886124
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.-2A>T rs764949869
NM_058195.4(CDKN2A):c.48C>T (p.Gly16=) rs786202556

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