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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 10

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HGVS	dbSNP	gnomAD frequency
NM_003722.5(TP63):c.*1181T>C	rs565556454	0.00153
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.1814G>A (p.Arg605Gln)	rs142981128	0.00011
NM_003722.5(TP63):c.1877T>G (p.Val626Gly)	rs372318389	0.00010
NM_003722.5(TP63):c.1367C>T (p.Pro456Leu)	rs201479097	0.00009
NM_003722.5(TP63):c.1083G>A (p.Lys361=)	rs148937466	0.00006
NM_003722.5(TP63):c.1465G>A (p.Ala489Thr)	rs138832017	0.00004
NM_003722.5(TP63):c.*2555dup	rs772929136

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