ClinVar Miner

List of variants in gene TP63 studied for Cleft Lip +/- Cleft Palate, Autosomal Dominant

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Gene type:
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Total variants: 64
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HGVS dbSNP
NM_003722.4(TP63):c.*2789A>G rs11708746
NM_003722.5(TP63):c.*101C>T rs574438859
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.*1386T>C rs35785527
NM_003722.5(TP63):c.*1464G>T rs571277874
NM_003722.5(TP63):c.*1472A>G rs375551286
NM_003722.5(TP63):c.*1620T>C rs34328757
NM_003722.5(TP63):c.*1702G>A rs886058232
NM_003722.5(TP63):c.*1844dup rs146332971
NM_003722.5(TP63):c.*1846C>T rs886058234
NM_003722.5(TP63):c.*1939T>G rs567626735
NM_003722.5(TP63):c.*1947dup rs140654135
NM_003722.5(TP63):c.*1959A>T rs527726173
NM_003722.5(TP63):c.*2002T>G rs35969817
NM_003722.5(TP63):c.*2009T>C rs886058236
NM_003722.5(TP63):c.*2123C>T rs36064124
NM_003722.5(TP63):c.*2139G>A rs35356690
NM_003722.5(TP63):c.*2155G>A rs573673077
NM_003722.5(TP63):c.*2197C>A rs886058237
NM_003722.5(TP63):c.*2205A>G rs886058238
NM_003722.5(TP63):c.*2216G>A rs35861864
NM_003722.5(TP63):c.*221G>A rs886058224
NM_003722.5(TP63):c.*2273A>G rs886058239
NM_003722.5(TP63):c.*2318G>A rs199834330
NM_003722.5(TP63):c.*232T>C rs569527175
NM_003722.5(TP63):c.*2345C>T rs35592567
NM_003722.5(TP63):c.*235_*238del rs886058225
NM_003722.5(TP63):c.*2426C>T rs568346565
NM_003722.5(TP63):c.*2477T>G rs186295449
NM_003722.5(TP63):c.*2544del rs201395656
NM_003722.5(TP63):c.*2555dup rs772929136
NM_003722.5(TP63):c.*2625A>T rs35694511
NM_003722.5(TP63):c.*2636del rs5855278
NM_003722.5(TP63):c.*2719_*2720del rs574327104
NM_003722.5(TP63):c.*295T>A rs886058226
NM_003722.5(TP63):c.*379T>A rs192879052
NM_003722.5(TP63):c.*382A>G rs886058227
NM_003722.5(TP63):c.*435C>T rs78233713
NM_003722.5(TP63):c.*45C>T rs34057105
NM_003722.5(TP63):c.*519C>T rs886058228
NM_003722.5(TP63):c.*541G>A rs73199799
NM_003722.5(TP63):c.*627T>C rs184452906
NM_003722.5(TP63):c.*638C>G rs6444406
NM_003722.5(TP63):c.*803G>A rs544230654
NM_003722.5(TP63):c.*854A>G rs187751631
NM_003722.5(TP63):c.*966C>T rs539983621
NM_003722.5(TP63):c.1374A>G (p.Ser458=) rs141794685
NM_003722.5(TP63):c.1531C>A (p.Pro511Thr) rs148076109
NM_003722.5(TP63):c.1587C>T (p.Leu529=) rs141847552
NM_003722.5(TP63):c.1644C>T (p.Ser548=) rs763019843
NM_003722.5(TP63):c.1652+14A>C rs150685395
NM_003722.5(TP63):c.1707G>A (p.Gly569=) rs202009057
NM_003722.5(TP63):c.1994T>G (p.Met665Arg) rs886058223
NM_003722.5(TP63):c.303G>A (p.Ser101=) rs186864205
NM_003722.5(TP63):c.409G>C (p.Asp137His) rs762935508
NM_003722.5(TP63):c.699A>G (p.Lys233=) rs199727371
NM_003722.5(TP63):c.766+3A>G rs886058221
NM_003722.5(TP63):c.766+5G>A rs374425727
NM_003722.5(TP63):c.859C>T (p.Leu287=) rs33979049
NM_003722.5(TP63):c.899C>A (p.Thr300Lys) rs886058222
NM_003722.5(TP63):c.992+4A>C rs534974406

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