ClinVar Miner

List of variants in gene TP63 reported as likely benign

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Gene type:
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Total variants: 34
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HGVS dbSNP
NM_003722.5(TP63):c.*101C>T rs574438859
NM_003722.5(TP63):c.*1386T>C rs35785527
NM_003722.5(TP63):c.*1464G>T rs571277874
NM_003722.5(TP63):c.*1620T>C rs34328757
NM_003722.5(TP63):c.*1939T>G rs567626735
NM_003722.5(TP63):c.*1959A>T rs527726173
NM_003722.5(TP63):c.*2002T>G rs35969817
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.*2216G>A rs35861864
NM_003722.5(TP63):c.*2318G>A rs199834330
NM_003722.5(TP63):c.*232T>C rs569527175
NM_003722.5(TP63):c.*2477T>G rs186295449
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.*379T>A rs192879052
NM_003722.5(TP63):c.*627T>C rs184452906
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.1531C>A (p.Pro511Thr) rs148076109
NM_003722.5(TP63):c.1587C>T (p.Leu529=) rs141847552
NM_003722.5(TP63):c.1652+14A>C rs150685395
NM_003722.5(TP63):c.1652+46G>A rs35558939
NM_003722.5(TP63):c.1707G>A (p.Gly569=) rs202009057
NM_003722.5(TP63):c.192-9_192-8del rs794727498
NM_003722.5(TP63):c.2034G>A (p.Glu678=) rs140508531
NM_003722.5(TP63):c.303G>A (p.Ser101=) rs186864205
NM_003722.5(TP63):c.699A>G (p.Lys233=) rs199727371
NM_003722.5(TP63):c.859C>T (p.Leu287=) rs33979049
NM_003722.5(TP63):c.876A>G (p.Pro292=) rs886038535
NM_003722.5(TP63):c.992+4A>C rs534974406

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