ClinVar Miner

List of variants in gene TP63 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 169
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HGVS dbSNP gnomAD frequency
NM_003722.5(TP63):c.1531C>A (p.Pro511Thr) rs148076109 0.00295
NM_003722.5(TP63):c.678C>T (p.Arg226=) rs61732782 0.00034
NM_003722.5(TP63):c.766+5G>A rs374425727 0.00022
NM_003722.5(TP63):c.2034G>A (p.Glu678=) rs140508531 0.00021
NM_003722.5(TP63):c.504C>T (p.Asn168=) rs141278696 0.00021
NM_003722.5(TP63):c.1599C>T (p.Ser533=) rs758093495 0.00018
NM_003722.5(TP63):c.993-18C>A rs376061503 0.00018
NM_003722.5(TP63):c.992+10G>A rs373106660 0.00016
NM_003722.5(TP63):c.579+8C>T rs994519414 0.00012
NM_003722.5(TP63):c.1464C>T (p.Asn488=) rs756653133 0.00011
NM_003722.5(TP63):c.1575C>T (p.Leu525=) rs147389337 0.00011
NM_003722.5(TP63):c.699A>G (p.Lys233=) rs199727371 0.00011
NM_003722.5(TP63):c.1459C>T (p.Arg487Cys) rs777306829 0.00009
NM_003722.5(TP63):c.1127G>A (p.Arg376His) rs143591434 0.00008
NM_003722.5(TP63):c.882+19A>T rs200703504 0.00008
NM_003722.5(TP63):c.1130-17C>T rs770730125 0.00007
NM_003722.5(TP63):c.255G>A (p.Ala85=) rs368463552 0.00007
NM_003722.5(TP63):c.1044A>G (p.Pro348=) rs370101210 0.00006
NM_003722.5(TP63):c.1095G>A (p.Ser365=) rs748609799 0.00006
NM_003722.5(TP63):c.1590C>T (p.Ser530=) rs373284695 0.00006
NM_003722.5(TP63):c.1707G>A (p.Gly569=) rs202009057 0.00006
NM_003722.5(TP63):c.387G>A (p.Ser129=) rs151335217 0.00006
NM_003722.5(TP63):c.1626G>A (p.Pro542=) rs370637253 0.00005
NM_003722.5(TP63):c.654A>G (p.Pro218=) rs764672477 0.00005
NM_003722.5(TP63):c.992+9C>T rs369838833 0.00005
NM_003722.5(TP63):c.1374A>G (p.Ser458=) rs141794685 0.00004
NM_003722.5(TP63):c.192-9A>G rs780843357 0.00004
NM_003722.5(TP63):c.63-1G>C rs200607940 0.00004
NM_003722.5(TP63):c.688G>C (p.Val230Leu) rs201466089 0.00004
NM_003722.5(TP63):c.1352C>G (p.Thr451Ser) rs747305746 0.00003
NM_003722.5(TP63):c.402T>C (p.Tyr134=) rs201239102 0.00003
NM_003722.5(TP63):c.714G>A (p.Thr238=) rs773030906 0.00003
NM_003722.5(TP63):c.900G>A (p.Thr300=) rs372807713 0.00003
NM_003722.5(TP63):c.992+8G>A rs192488893 0.00003
NM_003722.5(TP63):c.1413C>T (p.Ser471=) rs139407263 0.00002
NM_003722.5(TP63):c.1507+10T>C rs764929153 0.00002
NM_003722.5(TP63):c.1662G>A (p.Ala554=) rs755622591 0.00002
NM_003722.5(TP63):c.1761G>A (p.Leu587=) rs573105911 0.00002
NM_003722.5(TP63):c.2006G>A (p.Arg669His) rs369266838 0.00002
NM_003722.5(TP63):c.444C>G (p.Pro148=) rs150028891 0.00002
NM_003722.5(TP63):c.522G>A (p.Pro174=) rs780233345 0.00002
NM_003722.5(TP63):c.1110C>T (p.Asn370=) rs375593834 0.00001
NM_003722.5(TP63):c.1404A>G (p.Lys468=) rs753627633 0.00001
NM_003722.5(TP63):c.141T>C (p.Asn47=) rs768304711 0.00001
NM_003722.5(TP63):c.1527C>T (p.His509=) rs1720780438 0.00001
NM_003722.5(TP63):c.156A>G (p.Pro52=) rs780898702 0.00001
NM_003722.5(TP63):c.1644C>T (p.Ser548=) rs763019843 0.00001
NM_003722.5(TP63):c.1653-10C>T rs1720936506 0.00001
NM_003722.5(TP63):c.1746+10T>A rs1048355127 0.00001
NM_003722.5(TP63):c.1885G>A (p.Gly629Ser) rs769956674 0.00001
NM_003722.5(TP63):c.456C>T (p.Pro152=) rs774177255 0.00001
NM_003722.5(TP63):c.552G>A (p.Ser184=) rs755546487 0.00001
NM_003722.5(TP63):c.579+17C>T rs772881003 0.00001
NM_003722.5(TP63):c.708C>T (p.His236=) rs1217750983 0.00001
NM_003722.5(TP63):c.75C>T (p.Thr25=) rs773098305 0.00001
NM_003722.5(TP63):c.1002C>A (p.Val334=)
NM_003722.5(TP63):c.1005G>A (p.Leu335=)
NM_003722.5(TP63):c.1032C>T (p.Ile344=)
NM_003722.5(TP63):c.1107G>A (p.Lys369=)
NM_003722.5(TP63):c.1130-16A>G
NM_003722.5(TP63):c.1130-18G>A
NM_003722.5(TP63):c.1130-6C>T
NM_003722.5(TP63):c.1130-8T>C
NM_003722.5(TP63):c.1131G>A (p.Pro377=)
NM_003722.5(TP63):c.1155C>T (p.Ile385=)
NM_003722.5(TP63):c.1177C>A (p.Arg393=)
NM_003722.5(TP63):c.117C>T (p.Thr39=)
NM_003722.5(TP63):c.1201T>C (p.Leu401=)
NM_003722.5(TP63):c.1213-10A>G
NM_003722.5(TP63):c.1213-12T>A rs769860332
NM_003722.5(TP63):c.1213-17del rs375392004
NM_003722.5(TP63):c.1213-20C>T rs1352588675
NM_003722.5(TP63):c.1233T>C (p.Tyr411=)
NM_003722.5(TP63):c.1242G>A (p.Leu414=)
NM_003722.5(TP63):c.1251C>A (p.Ile417=)
NM_003722.5(TP63):c.1301C>T (p.Thr434Met) rs558374141
NM_003722.5(TP63):c.1302G>A (p.Thr434=)
NM_003722.5(TP63):c.1349+15G>A
NM_003722.5(TP63):c.144A>T (p.Glu48Asp)
NM_003722.5(TP63):c.1473T>C (p.Thr491=)
NM_003722.5(TP63):c.1491T>C (p.Asp497=)
NM_003722.5(TP63):c.1507+7G>A rs2108854610
NM_003722.5(TP63):c.1508-18C>T
NM_003722.5(TP63):c.150C>T (p.Leu50=) rs1577328344
NM_003722.5(TP63):c.1512C>T (p.Pro504=)
NM_003722.5(TP63):c.1581C>A (p.Pro527=)
NM_003722.5(TP63):c.1596A>G (p.Pro532=)
NM_003722.5(TP63):c.1602C>T (p.Thr534=)
NM_003722.5(TP63):c.1605C>G (p.Ser535=)
NM_003722.5(TP63):c.1608C>T (p.His536=) rs768312639
NM_003722.5(TP63):c.1617C>T (p.Pro539=)
NM_003722.5(TP63):c.1626G>T (p.Pro542=)
NM_003722.5(TP63):c.1652+14A>G rs150685395
NM_003722.5(TP63):c.1652+17T>C
NM_003722.5(TP63):c.1652+18G>A
NM_003722.5(TP63):c.1652+7C>T
NM_003722.5(TP63):c.1653-15C>T
NM_003722.5(TP63):c.1653-18_1653-5del
NM_003722.5(TP63):c.1677A>C (p.Ser559=)
NM_003722.5(TP63):c.1689C>T (p.Asp563=)
NM_003722.5(TP63):c.1701C>T (p.Thr567=) rs2108864854
NM_003722.5(TP63):c.1747-10T>G
NM_003722.5(TP63):c.1747-16_1747-15insCC
NM_003722.5(TP63):c.1747-18C>T
NM_003722.5(TP63):c.1767C>A (p.Ile589=)
NM_003722.5(TP63):c.1770T>C (p.Pro590=)
NM_003722.5(TP63):c.1780C>A (p.Arg594=)
NM_003722.5(TP63):c.1815G>A (p.Arg605=)
NM_003722.5(TP63):c.1824C>T (p.His608=) rs755722537
NM_003722.5(TP63):c.1852C>A (p.Arg618=)
NM_003722.5(TP63):c.1869C>T (p.Ala623=)
NM_003722.5(TP63):c.191+9A>G rs772213320
NM_003722.5(TP63):c.1971G>A (p.Glu657=)
NM_003722.5(TP63):c.1986C>T (p.Asn662=)
NM_003722.5(TP63):c.2022C>T (p.Arg674=)
NM_003722.5(TP63):c.276C>T (p.Ser92=)
NM_003722.5(TP63):c.27C>T (p.Ala9=)
NM_003722.5(TP63):c.324+11C>T rs1560147651
NM_003722.5(TP63):c.324+7G>A rs930341004
NM_003722.5(TP63):c.325-16C>G
NM_003722.5(TP63):c.325-7C>A
NM_003722.5(TP63):c.336G>A (p.Thr112=) rs267599728
NM_003722.5(TP63):c.378C>T (p.Asn126=)
NM_003722.5(TP63):c.405C>T (p.Asn135=) rs2108637496
NM_003722.5(TP63):c.435G>A (p.Ala145=)
NM_003722.5(TP63):c.435G>C (p.Ala145=) rs546908184
NM_003722.5(TP63):c.448G>A (p.Ala150Thr) rs762371837
NM_003722.5(TP63):c.459C>T (p.Ser153=)
NM_003722.5(TP63):c.465C>G (p.Thr155=)
NM_003722.5(TP63):c.465C>T (p.Thr155=)
NM_003722.5(TP63):c.475C>T (p.Leu159Phe) rs752603187
NM_003722.5(TP63):c.489C>T (p.Pro163=)
NM_003722.5(TP63):c.540C>T (p.Ser180=)
NM_003722.5(TP63):c.552G>T (p.Ser184=)
NM_003722.5(TP63):c.561C>G (p.Ala187=)
NM_003722.5(TP63):c.567G>A (p.Ser189=)
NM_003722.5(TP63):c.579+11C>T
NM_003722.5(TP63):c.579+16A>G
NM_003722.5(TP63):c.579+18G>A
NM_003722.5(TP63):c.580-17G>T
NM_003722.5(TP63):c.62+18A>G
NM_003722.5(TP63):c.624A>G (p.Thr208=)
NM_003722.5(TP63):c.63-18C>A
NM_003722.5(TP63):c.63-20T>A rs2108795452
NM_003722.5(TP63):c.711C>T (p.Val237=)
NM_003722.5(TP63):c.738C>T (p.Asn246=)
NM_003722.5(TP63):c.762C>T (p.Asn254=)
NM_003722.5(TP63):c.766+11T>C
NM_003722.5(TP63):c.767-17del
NM_003722.5(TP63):c.825T>C (p.Tyr275=) rs773649260
NM_003722.5(TP63):c.840C>T (p.Ile280=)
NM_003722.5(TP63):c.861G>A (p.Leu287=)
NM_003722.5(TP63):c.882+17C>T
NM_003722.5(TP63):c.882+18A>G
NM_003722.5(TP63):c.882+20A>C
NM_003722.5(TP63):c.882+8G>A
NM_003722.5(TP63):c.883-10T>C
NM_003722.5(TP63):c.883-15A>G rs1717919445
NM_003722.5(TP63):c.888C>T (p.Gly296=)
NM_003722.5(TP63):c.891T>G (p.Thr297=)
NM_003722.5(TP63):c.894A>G (p.Glu298=) rs2108804339
NM_003722.5(TP63):c.912C>T (p.Tyr304=)
NM_003722.5(TP63):c.918C>T (p.Phe306=)
NM_003722.5(TP63):c.936T>C (p.Cys312=) rs2108804403
NM_003722.5(TP63):c.945G>A (p.Gly315=)
NM_003722.5(TP63):c.96A>G (p.Lys32=)
NM_003722.5(TP63):c.992+19A>G
NM_003722.5(TP63):c.993-15T>C
NM_003722.5(TP63):c.996G>A (p.Gly332=)

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