ClinVar Miner

List of variants in gene TP63 reported by Preventiongenetics, part of Exact Sciences

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Gene type:
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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_003722.5(TP63):c.1350-23T>C rs1345186 0.74615
NM_003722.5(TP63):c.1130-22A>G rs6789961 0.32652
NM_003722.5(TP63):c.1349+41G>A rs9840360 0.25021
NM_003722.5(TP63):c.766+42G>A rs2276792 0.19026
NM_003722.5(TP63):c.766+34T>G rs17514215 0.11812
NM_003722.5(TP63):c.*45C>T rs34057105 0.05395
NM_003722.5(TP63):c.191+24T>C rs34875865 0.03673
NM_003722.5(TP63):c.1652+46G>A rs35558939 0.03124
NM_003722.5(TP63):c.859C>T (p.Leu287=) rs33979049 0.01380
NM_003722.5(TP63):c.1587C>T (p.Leu529=) rs141847552 0.00082
NM_003722.5(TP63):c.1459C>T (p.Arg487Cys) rs777306829 0.00009
NM_003722.5(TP63):c.109C>T (p.Arg37Ter) rs147340040 0.00001
NM_003722.5(TP63):c.1553G>A (p.Gly518Glu) rs1478677560 0.00001
NM_003722.5(TP63):c.1034G>T (p.Cys345Phe)
NM_003722.5(TP63):c.122C>T (p.Ser41Phe)
NM_003722.5(TP63):c.1315C>A (p.Gln439Lys)
NM_003722.5(TP63):c.1349+40G>C rs9840359
NM_003722.5(TP63):c.1350-34T>G rs1554131
NM_003722.5(TP63):c.1583C>G (p.Pro528Arg)
NM_003722.5(TP63):c.1727T>C (p.Ile576Thr) rs1057517841
NM_003722.5(TP63):c.1769C>T (p.Pro590Leu) rs2108873027
NM_003722.5(TP63):c.2005C>T (p.Arg669Cys)
NM_003722.5(TP63):c.361G>A (p.Asp121Asn)
NM_003722.5(TP63):c.530T>C (p.Phe177Ser)
NM_003722.5(TP63):c.587C>A (p.Thr196Asn)
NM_003722.5(TP63):c.739C>G (p.His247Asp)
NM_003722.5(TP63):c.876A>G (p.Pro292=) rs886038535
NM_003722.5(TP63):c.940G>A (p.Gly314Arg)
NM_003722.5(TP63):c.944G>A (p.Gly315Glu)
NM_003722.5(TP63):c.952C>T (p.Arg318Cys) rs1205536026
NM_003722.5(TP63):c.970_972del (p.Ile324del) rs2108804508

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