List of variants in gene TP63 reported as likely pathogenic for not provided

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_003722.5(TP63):c.1007G>A (p.Gly336Asp)	rs2108806204
NM_003722.5(TP63):c.1010G>A (p.Arg337Gln)	rs113993967
NM_003722.5(TP63):c.1048A>G (p.Arg350Gly)	rs1057517985
NM_003722.5(TP63):c.1177C>T (p.Arg393Ter)	rs941268998
NM_003722.5(TP63):c.1655T>G (p.Phe552Cys)	rs886039443
NM_003722.5(TP63):c.1682G>A (p.Cys561Tyr)	rs1057518399
NM_003722.5(TP63):c.1717_1719dup (p.Ile573dup)	rs2108864901
NM_003722.5(TP63):c.1769C>T (p.Pro590Leu)	rs2108873027
NM_003722.5(TP63):c.1820T>C (p.Leu607Pro)	rs1440083511
NM_003722.5(TP63):c.1922C>T (p.Ala641Val)	rs1064793283
NM_003722.5(TP63):c.1927C>T (p.Arg643Ter)	rs1560311554
NM_003722.5(TP63):c.1963C>T (p.Arg655Ter)
NM_003722.5(TP63):c.517G>C (p.Gly173Arg)	rs1057521750
NM_003722.5(TP63):c.566C>T (p.Ser189Leu)	rs866938979
NM_003722.5(TP63):c.605A>G (p.Tyr202Cys)	rs1057517984
NM_003722.5(TP63):c.853_854del (p.Ser285fs)	rs1553857303
NM_003722.5(TP63):c.934T>G (p.Cys312Gly)
NM_003722.5(TP63):c.942_944del (p.Gly315del)	rs1057518137
NM_003722.5(TP63):c.970_972del (p.Ile324del)	rs2108804508

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