List of variants in gene TP63 reported as uncertain significance 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: 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.1367C>T (p.Pro456Leu)	rs201479097	0.00009
NM_003722.5(TP63):c.2021G>A (p.Arg674His)	rs34713855	0.00006
NM_003722.5(TP63):c.1553G>A (p.Gly518Glu)	rs1478677560	0.00001
NM_003722.5(TP63):c.1009C>T (p.Arg337Ter)
NM_003722.5(TP63):c.1013G>A (p.Arg338His)	rs1029852196
NM_003722.5(TP63):c.1204T>C (p.Tyr402His)	rs926502142
NM_003722.5(TP63):c.1583C>A (p.Pro528Gln)	rs761041436
NM_003722.5(TP63):c.1805T>C (p.Leu602Pro)	rs760032006
NM_003722.5(TP63):c.19C>T (p.Arg7Trp)
NM_003722.5(TP63):c.383C>T (p.Ser128Phe)	rs2108637329
NM_003722.5(TP63):c.487C>T (p.Pro163Ser)	rs1560204733
NM_003722.5(TP63):c.580-3C>G

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