List of variants in gene TP63 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
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: 26

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HGVS	dbSNP	gnomAD frequency
NM_003722.5(TP63):c.1652+46G>A	rs35558939	0.03025
NM_003722.5(TP63):c.882+321T>G	rs77881428	0.01396
NM_003722.5(TP63):c.767-333C>T	rs79616899	0.01391
NM_003722.5(TP63):c.325-268A>G	rs73889827	0.01357
NM_003722.5(TP63):c.1508-29C>A	rs74577755	0.01249
NM_003722.5(TP63):c.325-18195A>G	rs116027224	0.01212
NM_003722.5(TP63):c.883-88G>C	rs114009645	0.01070
NM_003722.5(TP63):c.62+225C>T	rs77398377	0.00850
NM_003722.5(TP63):c.1508-126C>T	rs73892204	0.00687
NM_003722.5(TP63):c.192-287A>G	rs115807793	0.00671
NM_003722.5(TP63):c.1507+300T>C	rs73892203	0.00661
NM_003722.5(TP63):c.1350-56A>C	rs190206412	0.00615
NM_003722.5(TP63):c.1350-6145G>A	rs35477020	0.00590
NM_003722.5(TP63):c.767-93T>C	rs150454894	0.00479
NM_003722.5(TP63):c.1350-62A>G	rs111536509	0.00448
NM_003722.5(TP63):c.62+25231C>T	rs148095450	0.00304
NM_003722.5(TP63):c.883-139A>G	rs145952254	0.00276
NM_003722.5(TP63):c.2034G>A (p.Glu678=)	rs140508531	0.00021
NM_003722.5(TP63):c.1599C>T (p.Ser533=)	rs758093495	0.00017
NM_003722.5(TP63):c.374A>C (p.Gln125Pro)	rs982556895	0.00013
NM_003722.5(TP63):c.1129+202A>C	rs147687119
NM_003722.5(TP63):c.191+275A>C	rs75754687
NM_003722.5(TP63):c.325-18252dup	rs557500463
NM_003722.5(TP63):c.579+158T>A	rs149006192
NM_003722.5(TP63):c.766+104C>T	rs146216522
NM_003722.5(TP63):c.766+105G>A	rs112063994

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