List of variants in gene TP63 reported as benign by PreventionGenetics, part of Exact Sciences

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_003722.5(TP63):c.1350-23T>C	rs1345186	0.74615
NM_003722.5(TP63):c.1130-22A>G	rs6789961	0.32652
NM_003722.5(TP63):c.1349+41G>A	rs9840360	0.25021
NM_003722.5(TP63):c.766+42G>A	rs2276792	0.19026
NM_003722.5(TP63):c.766+34T>G	rs17514215	0.11812
NM_003722.5(TP63):c.*45C>T	rs34057105	0.05395
NM_003722.5(TP63):c.191+24T>C	rs34875865	0.03673
NM_003722.5(TP63):c.859C>T (p.Leu287=)	rs33979049	0.01380
NM_003722.5(TP63):c.1788G>A (p.Ala596=)	rs148577576	0.00180
NM_003722.5(TP63):c.1349+40G>C	rs9840359
NM_003722.5(TP63):c.1350-34T>G	rs1554131

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