List of variants in gene TP63 reported as likely 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: 20

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HGVS	dbSNP	gnomAD frequency
NM_003722.5(TP63):c.1652+46G>A	rs35558939	0.03124
NM_003722.5(TP63):c.1587C>T (p.Leu529=)	rs141847552	0.00082
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.1599C>T (p.Ser533=)	rs758093495	0.00018
NM_003722.5(TP63):c.374A>C (p.Gln125Pro)	rs982556895	0.00013
NM_003722.5(TP63):c.699A>G (p.Lys233=)	rs199727371	0.00011
NM_003722.5(TP63):c.1127G>A (p.Arg376His)	rs143591434	0.00008
NM_003722.5(TP63):c.1626G>A (p.Pro542=)	rs370637253	0.00005
NM_003722.5(TP63):c.1213-4A>G	rs763128484	0.00002
NM_003722.5(TP63):c.1404A>G (p.Lys468=)	rs753627633	0.00001
NM_003722.5(TP63):c.1527C>T (p.His509=)	rs1720780438	0.00001
NM_003722.5(TP63):c.1002C>A (p.Val334=)
NM_003722.5(TP63):c.114C>T (p.Ser38=)
NM_003722.5(TP63):c.1507+8C>T
NM_003722.5(TP63):c.1677A>C (p.Ser559=)
NM_003722.5(TP63):c.1770T>C (p.Pro590=)
NM_003722.5(TP63):c.20G>T (p.Arg7Leu)	rs568702479
NM_003722.5(TP63):c.444C>T (p.Pro148=)
NM_003722.5(TP63):c.876A>G (p.Pro292=)	rs886038535

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