ClinVar Miner

List of variants in gene TP63 reported as uncertain significance

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Total variants: 59
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HGVS dbSNP
NC_000003.11:g.(?_189582001)_(189590804_?)del
NM_003722.5(TP63):c.*1130_*1133del rs886058229
NM_003722.5(TP63):c.*1164A>G rs886058230
NM_003722.5(TP63):c.*1181T>C rs565556454
NM_003722.5(TP63):c.*1217T>C rs886058231
NM_003722.5(TP63):c.*1472A>G rs375551286
NM_003722.5(TP63):c.*1702G>A rs886058232
NM_003722.5(TP63):c.*1846C>T rs886058234
NM_003722.5(TP63):c.*1947dup rs140654135
NM_003722.5(TP63):c.*2009T>C rs886058236
NM_003722.5(TP63):c.*2197C>A rs886058237
NM_003722.5(TP63):c.*2205A>G rs886058238
NM_003722.5(TP63):c.*221G>A rs886058224
NM_003722.5(TP63):c.*2273A>G rs886058239
NM_003722.5(TP63):c.*235_*238del rs886058225
NM_003722.5(TP63):c.*2426C>T rs568346565
NM_003722.5(TP63):c.*2555dup rs772929136
NM_003722.5(TP63):c.*295T>A rs886058226
NM_003722.5(TP63):c.*382A>G rs886058227
NM_003722.5(TP63):c.*519C>T rs886058228
NM_003722.5(TP63):c.1013G>A (p.Arg338His) rs1029852196
NM_003722.5(TP63):c.1042C>G (p.Pro348Ala)
NM_003722.5(TP63):c.1043C>T (p.Pro348Leu) rs1560280393
NM_003722.5(TP63):c.1083G>A (p.Lys361=) rs148937466
NM_003722.5(TP63):c.109C>T (p.Arg37Ter)
NM_003722.5(TP63):c.1374A>G (p.Ser458=) rs141794685
NM_003722.5(TP63):c.1528A>T (p.Met510Leu)
NM_003722.5(TP63):c.1553G>A (p.Gly518Glu) rs1478677560
NM_003722.5(TP63):c.1644C>T (p.Ser548=) rs763019843
NM_003722.5(TP63):c.1653-9C>T rs886044632
NM_003722.5(TP63):c.1746+5G>A rs1553863040
NM_003722.5(TP63):c.1748A>T (p.Asp583Val)
NM_003722.5(TP63):c.1805T>C (p.Leu602Pro) rs760032006
NM_003722.5(TP63):c.1827A>G (p.Glu609=) rs147538847
NM_003722.5(TP63):c.191+5G>C rs1553824695
NM_003722.5(TP63):c.1910G>T (p.Arg637Leu) rs770997588
NM_003722.5(TP63):c.1994T>G (p.Met665Arg) rs886058223
NM_003722.5(TP63):c.254C>T (p.Ala85Val)
NM_003722.5(TP63):c.290G>A (p.Arg97His) rs752080701
NM_003722.5(TP63):c.325-18439A>G rs779762640
NM_003722.5(TP63):c.371T>C (p.Ile124Thr) rs1553845417
NM_003722.5(TP63):c.394A>G (p.Ser132Gly)
NM_003722.5(TP63):c.409G>C (p.Asp137His) rs762935508
NM_003722.5(TP63):c.435G>C (p.Ala145=) rs546908184
NM_003722.5(TP63):c.487C>T (p.Pro163Ser) rs1560204733
NM_003722.5(TP63):c.497C>A (p.Pro166His) rs1560204773
NM_003722.5(TP63):c.504C>T (p.Asn168=) rs141278696
NM_003722.5(TP63):c.517G>C (p.Gly173Arg) rs1057521750
NM_003722.5(TP63):c.63-1G>C rs200607940
NM_003722.5(TP63):c.677G>A (p.Arg226His) rs193921145
NM_003722.5(TP63):c.678C>T (p.Arg226=) rs61732782
NM_003722.5(TP63):c.698A>C (p.Lys233Thr) rs1553856533
NM_003722.5(TP63):c.738C>G (p.Asn246Lys)
NM_003722.5(TP63):c.766+3A>G rs886058221
NM_003722.5(TP63):c.766+5G>A rs374425727
NM_003722.5(TP63):c.899C>A (p.Thr300Lys) rs886058222
NM_003722.5(TP63):c.927_929CAG[1] (p.Ser311del)
NM_003722.5(TP63):c.935G>T (p.Cys312Phe)
NM_003722.5(TP63):c.992+10G>A rs373106660

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