ClinVar Miner

List of variants in gene TP63 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 126
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HGVS dbSNP gnomAD frequency
NM_003722.5(TP63):c.882+304G>A rs6807129 0.88343
NM_003722.5(TP63):c.1350-23T>C rs1345186 0.74615
NM_003722.5(TP63):c.63-30964A>T rs4687085 0.70419
NM_003722.5(TP63):c.1130-237T>C rs7624324 0.68909
NM_003722.5(TP63):c.767-338A>G rs3773929 0.60604
NM_003722.5(TP63):c.1212+79A>G rs6790167 0.53718
NM_003722.5(TP63):c.992+299T>G rs1399773 0.47005
NM_003722.5(TP63):c.62+24991T>A rs4505678 0.43515
NM_003722.5(TP63):c.62+25276G>C rs9853796 0.43515
NM_003722.5(TP63):c.62+24867G>T rs1920245 0.43506
NM_003722.5(TP63):c.63-6311C>T rs10937410 0.39210
NM_003722.5(TP63):c.62+49875T>C rs9846059 0.34015
NM_003722.5(TP63):c.1130-22A>G rs6789961 0.32652
NM_003722.5(TP63):c.62+50167A>G rs1920283 0.32217
NM_003722.5(TP63):c.992+121C>T rs7653848 0.28380
NM_003722.5(TP63):c.*2345C>T rs35592567 0.20615
NM_003722.5(TP63):c.766+42G>A rs2276792 0.19026
NM_003722.5(TP63):c.62+49783A>G rs73195974 0.18039
NM_003722.5(TP63):c.63-336A>G rs75548317 0.17506
NM_003722.5(TP63):c.993-187A>G rs1399774 0.16689
NM_003722.5(TP63):c.1129+296dup rs34188015 0.16671
NM_003722.5(TP63):c.191+254C>G rs74612319 0.13168
NM_003722.5(TP63):c.766+34T>G rs17514215 0.11812
NM_003722.5(TP63):c.62+50004G>A rs11709407 0.10104
NM_003722.5(TP63):c.1507+269A>G rs2166815 0.05890
NM_003722.5(TP63):c.766+294A>G rs11716871 0.05636
NM_003722.5(TP63):c.*45C>T rs34057105 0.05395
NM_003722.5(TP63):c.*2216G>A rs35861864 0.05107
NM_003722.5(TP63):c.*2636del rs5855278 0.03709
NM_003722.5(TP63):c.1507+264C>T rs35530903 0.03677
NM_003722.5(TP63):c.63-6066G>A rs77778969 0.03391
NM_003722.5(TP63):c.1652+46G>A rs35558939 0.03124
NM_003722.5(TP63):c.1653-264C>T rs11923292 0.02981
NM_003722.5(TP63):c.324+76T>C rs76191543 0.02260
NM_003722.5(TP63):c.1130-283A>G rs79621548 0.02162
NM_003722.5(TP63):c.62+50063C>T rs58267455 0.02079
NM_003722.5(TP63):c.62+49918G>A rs73892306 0.01522
NM_003722.5(TP63):c.882+321T>G rs77881428 0.01390
NM_003722.5(TP63):c.767-333C>T rs79616899 0.01383
NM_003722.5(TP63):c.859C>T (p.Leu287=) rs33979049 0.01380
NM_003722.5(TP63):c.325-268A>G rs73889827 0.01357
NM_003722.5(TP63):c.1508-29C>A rs74577755 0.01345
NM_003722.5(TP63):c.325-18195A>G rs116027224 0.01212
NM_003722.5(TP63):c.883-88G>C rs114009645 0.01070
NM_003722.5(TP63):c.62+225C>T rs77398377 0.00850
NM_003722.5(TP63):c.1507+300T>C rs73892203 0.00710
NM_003722.5(TP63):c.1508-126C>T rs73892204 0.00687
NM_003722.5(TP63):c.192-287A>G rs115807793 0.00671
NM_003722.5(TP63):c.1350-6145G>A rs35477020 0.00642
NM_003722.5(TP63):c.1350-56A>C rs190206412 0.00615
NM_003722.5(TP63):c.767-93T>C rs150454894 0.00479
NM_003722.5(TP63):c.1350-62A>G rs111536509 0.00448
NM_003722.5(TP63):c.62+25231C>T rs148095450 0.00304
NM_003722.5(TP63):c.1531C>A (p.Pro511Thr) rs148076109 0.00295
NM_003722.5(TP63):c.580-11A>T rs148217164 0.00131
NM_003722.5(TP63):c.1587C>T (p.Leu529=) rs141847552 0.00082
NM_003722.5(TP63):c.2034G>A (p.Glu678=) rs140508531 0.00021
NM_003722.5(TP63):c.1599C>T (p.Ser533=) rs758093495 0.00018
NM_003722.5(TP63):c.374A>C (p.Gln125Pro) rs982556895 0.00013
NM_003722.5(TP63):c.1814G>A (p.Arg605Gln) rs142981128 0.00011
NM_003722.5(TP63):c.1367C>T (p.Pro456Leu) rs201479097 0.00009
NM_003722.5(TP63):c.1127G>A (p.Arg376His) rs143591434 0.00008
NM_003722.5(TP63):c.2021G>A (p.Arg674His) rs34713855 0.00006
NM_003722.5(TP63):c.366G>A (p.Gln122=) rs201774402 0.00003
NC_000003.12:g.189897324C>T rs1346662870 0.00001
NM_003722.5(TP63):c.1553G>A (p.Gly518Glu) rs1478677560 0.00001
NM_003722.5(TP63):c.727C>T (p.Arg243Trp) rs121908835 0.00001
NM_003722.5(TP63):c.728G>A (p.Arg243Gln) rs121908836 0.00001
NM_003722.5(TP63):c.767-40A>G rs542685647 0.00001
NM_003722.5(TP63):c.992+4A>C rs534974406 0.00001
NM_001114980.2(TP63):c.26del (p.Gln9fs) rs1553840705
NM_003722.5(TP63):c.*2544del rs201395656
NM_003722.5(TP63):c.1009C>T (p.Arg337Ter)
NM_003722.5(TP63):c.1013G>A (p.Arg338His) rs1029852196
NM_003722.5(TP63):c.1027C>T (p.Arg343Trp) rs886041251
NM_003722.5(TP63):c.1028G>A (p.Arg343Gln) rs121908841
NM_003722.5(TP63):c.1039T>C (p.Cys347Arg)
NM_003722.5(TP63):c.1040G>T (p.Cys347Phe) rs1064793282
NM_003722.5(TP63):c.1048A>G (p.Arg350Gly) rs1057517985
NM_003722.5(TP63):c.1052A>G (p.Asp351Gly) rs121908844
NM_003722.5(TP63):c.1129+125C>G rs16864880
NM_003722.5(TP63):c.1129+202A>C rs147687119
NM_003722.5(TP63):c.1177C>T (p.Arg393Ter) rs941268998
NM_003722.5(TP63):c.1204T>C (p.Tyr402His) rs926502142
NM_003722.5(TP63):c.1349+269G>T rs9844653
NM_003722.5(TP63):c.1349+40G>T rs9840359
NM_003722.5(TP63):c.1350-34T>C rs1554131
NM_003722.5(TP63):c.1583C>A (p.Pro528Gln) rs761041436
NM_003722.5(TP63):c.1655T>G (p.Phe552Cys) rs886039443
NM_003722.5(TP63):c.1682G>A (p.Cys561Tyr) rs1057518399
NM_003722.5(TP63):c.1727T>C (p.Ile576Thr) rs1057517841
NM_003722.5(TP63):c.1769C>T (p.Pro590Leu) rs2108873027
NM_003722.5(TP63):c.1805T>C (p.Leu602Pro) rs760032006
NM_003722.5(TP63):c.1820T>C (p.Leu607Pro) rs1440083511
NM_003722.5(TP63):c.191+275A>C rs75754687
NM_003722.5(TP63):c.192-9_192-8del rs794727498
NM_003722.5(TP63):c.1922C>T (p.Ala641Val) rs1064793283
NM_003722.5(TP63):c.1927C>T (p.Arg643Ter) rs1560311554
NM_003722.5(TP63):c.19C>T (p.Arg7Trp)
NM_003722.5(TP63):c.324+166C>G rs4686525
NM_003722.5(TP63):c.325-18252dup rs557500463
NM_003722.5(TP63):c.325-75_325-74del rs2108636745
NM_003722.5(TP63):c.383C>T (p.Ser128Phe) rs2108637329
NM_003722.5(TP63):c.487C>T (p.Pro163Ser) rs1560204733
NM_003722.5(TP63):c.517G>C (p.Gly173Arg) rs1057521750
NM_003722.5(TP63):c.518G>T (p.Gly173Val) rs113993965
NM_003722.5(TP63):c.547C>T (p.Gln183Ter) rs1057520750
NM_003722.5(TP63):c.566C>T (p.Ser189Leu) rs866938979
NM_003722.5(TP63):c.579+158T>A rs149006192
NM_003722.5(TP63):c.579+39T>A rs34429985
NM_003722.5(TP63):c.580-3C>G
NM_003722.5(TP63):c.605A>G (p.Tyr202Cys) rs1057517984
NM_003722.5(TP63):c.63-149A>G rs76313891
NM_003722.5(TP63):c.63-6274G>T rs11922764
NM_003722.5(TP63):c.63-6388del rs59444552
NM_003722.5(TP63):c.740A>G (p.His247Arg) rs864621968
NM_003722.5(TP63):c.766+104C>T rs146216522
NM_003722.5(TP63):c.766+105G>A rs112063994
NM_003722.5(TP63):c.797G>A (p.Arg266Gln) rs121908849
NM_003722.5(TP63):c.883-139A>G
NM_003722.5(TP63):c.935G>A (p.Cys312Tyr) rs1057520664
NM_003722.5(TP63):c.942_944del (p.Gly315del) rs1057518137
NM_003722.5(TP63):c.952C>T (p.Arg318Cys) rs1205536026
NM_003722.5(TP63):c.953G>A (p.Arg318His) rs121908840
NM_003722.5(TP63):c.955C>T (p.Arg319Cys) rs121908839
NM_003722.5(TP63):c.956G>A (p.Arg319His) rs886039442

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