ClinVar Miner

List of variants in gene TP63 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_003722.5(TP63):c.882+304G>A rs6807129 0.88375
NM_003722.5(TP63):c.1349+269G>T rs9844653 0.82546
NM_003722.5(TP63):c.1350-23T>C rs1345186 0.74615
NM_003722.5(TP63):c.63-30964A>T rs4687085 0.70136
NM_003722.5(TP63):c.1130-237T>C rs7624324 0.68909
NM_003722.5(TP63):c.767-338A>G rs3773929 0.60192
NM_003722.5(TP63):c.1212+79A>G rs6790167 0.52977
NM_003722.5(TP63):c.992+299T>G rs1399773 0.46197
NM_003722.5(TP63):c.62+24991T>A rs4505678 0.43958
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.62+50167A>G rs1920283 0.32217
NM_003722.5(TP63):c.1130-22A>G rs6789961 0.31702
NM_003722.5(TP63):c.992+121C>T rs7653848 0.27611
NM_003722.5(TP63):c.1349+41G>A rs9840360 0.25021
NM_003722.5(TP63):c.*2345C>T rs35592567 0.20511
NM_003722.5(TP63):c.766+42G>A rs2276792 0.19026
NM_003722.5(TP63):c.62+49783A>G rs73195974 0.18234
NM_003722.5(TP63):c.63-336A>G rs75548317 0.17717
NC_000003.12:g.189897291A>G rs11708746 0.16914
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 0.13259
NM_003722.5(TP63):c.766+34T>G rs17514215 0.11812
NM_003722.5(TP63):c.62+50004G>A rs11709407 0.10145
NM_003722.5(TP63):c.*541G>A rs73199799 0.09298
NM_003722.5(TP63):c.766+294A>G rs11716871 0.05636
NM_003722.5(TP63):c.1507+269A>G rs2166815 0.05528
NM_003722.5(TP63):c.*45C>T rs34057105 0.05395
NM_003722.5(TP63):c.*2216G>A rs35861864 0.05054
NM_003722.5(TP63):c.*435C>T rs78233713 0.04622
NM_003722.5(TP63):c.*2636del rs5855278 0.03709
NM_003722.5(TP63):c.191+24T>C rs34875865 0.03673
NM_003722.5(TP63):c.1507+264C>T rs35530903 0.03458
NM_003722.5(TP63):c.63-6066G>A rs77778969 0.03391
NM_003722.5(TP63):c.1653-264C>T rs11923292 0.02772
NM_003722.5(TP63):c.324+76T>C rs76191543 0.02112
NM_003722.5(TP63):c.62+50063C>T rs58267455 0.02079
NM_003722.5(TP63):c.1130-283A>G rs79621548 0.02015
NM_003722.5(TP63):c.62+49918G>A rs73892306 0.01415
NM_003722.5(TP63):c.859C>T (p.Leu287=) rs33979049 0.01383
NM_003722.5(TP63):c.*1939T>G rs567626735 0.00308
NM_003722.5(TP63):c.1531C>A (p.Pro511Thr) rs148076109 0.00301
NM_003722.5(TP63):c.*1181T>C rs565556454 0.00153
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.992+4A>C rs534974406 0.00022
NM_003722.5(TP63):c.1127G>A (p.Arg376His) rs143591434 0.00007
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.767-40A>G rs542685647 0.00001
NM_003722.5(TP63):c.*2544del rs201395656
NM_003722.5(TP63):c.*2555dup rs772929136
NM_003722.5(TP63):c.1129+125C>G rs16864880
NM_003722.5(TP63):c.1349+40G>C rs9840359
NM_003722.5(TP63):c.1349+40G>T rs9840359
NM_003722.5(TP63):c.1350-34T>C rs1554131
NM_003722.5(TP63):c.1350-34T>G rs1554131
NM_003722.5(TP63):c.192-9_192-8del rs794727498
NM_003722.5(TP63):c.324+166C>G rs4686525
NM_003722.5(TP63):c.325-75_325-74del rs2108636745
NM_003722.5(TP63):c.579+39T>A rs34429985
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

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