Variants in gene TP63 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 11

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HGVS	dbSNP	gnomAD frequency
NM_003722.5(TP63):c.678C>T (p.Arg226=)	rs61732782	0.00034
NM_003722.5(TP63):c.1827A>G (p.Glu609=)	rs147538847	0.00031
NM_003722.5(TP63):c.504C>T (p.Asn168=)	rs141278696	0.00021
NM_003722.5(TP63):c.992+10G>A	rs373106660	0.00016
NM_003722.5(TP63):c.374A>C (p.Gln125Pro)	rs982556895	0.00013
NM_003722.5(TP63):c.1459C>T (p.Arg487Cys)	rs777306829	0.00009
NM_003722.5(TP63):c.992+9C>T	rs369838833	0.00005
NM_003722.5(TP63):c.688G>C (p.Val230Leu)	rs201466089	0.00004
NM_003722.5(TP63):c.1761G>A (p.Leu587=)	rs573105911	0.00002
NM_003722.5(TP63):c.1644C>T (p.Ser548=)	rs763019843	0.00001
NM_003722.5(TP63):c.435G>C (p.Ala145=)	rs546908184

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