List of variants reported as uncertain significance for ADULT syndrome; Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome; Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3; Limb-mammary syndrome; Rapp-Hodgkin syndrome; Split hand-foot malformation 4; Orofacial cleft 8

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_003722.5(TP63):c.1814G>A (p.Arg605Gln)	rs142981128	0.00011
NM_003722.5(TP63):c.1121C>T (p.Thr374Met)	rs199807776	0.00009
NM_003722.5(TP63):c.2021G>A (p.Arg674His)	rs34713855	0.00005
NM_003722.5(TP63):c.1352C>G (p.Thr451Ser)	rs747305746	0.00003
NM_003722.5(TP63):c.1697C>T (p.Thr566Met)	rs745687224	0.00003
NM_003722.5(TP63):c.50C>G (p.Pro17Arg)	rs1408730457	0.00003
NM_003722.5(TP63):c.110G>A (p.Arg37Gln)	rs754361670	0.00002
NM_003722.5(TP63):c.1394C>T (p.Pro465Leu)	rs775037738	0.00001
NM_003722.5(TP63):c.1612A>G (p.Thr538Ala)	rs565094952	0.00001
NM_003722.5(TP63):c.1825G>A (p.Glu609Lys)	rs142762485	0.00001
NM_003722.5(TP63):c.2003G>A (p.Arg668His)	rs758317410	0.00001
NM_003722.5(TP63):c.62G>A (p.Arg21His)	rs766583971	0.00001
NM_003722.5(TP63):c.1831TCC[1] (p.Ser612del)	rs1294809942

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