List of variants in gene TP63 reported as likely benign for EEC syndrome

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_003722.5(TP63):c.1531C>A (p.Pro511Thr)	rs148076109	0.00295
NM_003722.5(TP63):c.1788G>A (p.Ala596=)	rs148577576	0.00180
NM_003722.5(TP63):c.498C>T (p.Pro166=)	rs146612442	0.00041
NM_003722.5(TP63):c.1599C>T (p.Ser533=)	rs758093495	0.00018
NM_003722.5(TP63):c.1575C>T (p.Leu525=)	rs147389337	0.00011
NM_003722.5(TP63):c.699A>G (p.Lys233=)	rs199727371	0.00011
NM_003722.5(TP63):c.84T>G (p.His28Gln)	rs370716448	0.00009
NM_003722.5(TP63):c.882+19A>T	rs200703504	0.00008
NM_003722.5(TP63):c.1095G>A (p.Ser365=)	rs748609799	0.00006
NM_003722.5(TP63):c.1707G>A (p.Gly569=)	rs202009057	0.00006
NM_003722.5(TP63):c.1626G>A (p.Pro542=)	rs370637253	0.00005
NM_003722.5(TP63):c.654A>G (p.Pro218=)	rs764672477	0.00005
NM_003722.5(TP63):c.1374A>G (p.Ser458=)	rs141794685	0.00004
NM_003722.5(TP63):c.63-1G>C	rs200607940	0.00004
NM_003722.5(TP63):c.688G>C (p.Val230Leu)	rs201466089	0.00004
NM_003722.5(TP63):c.366G>A (p.Gln122=)	rs201774402	0.00003
NM_003722.5(TP63):c.402T>C (p.Tyr134=)	rs201239102	0.00003
NM_003722.5(TP63):c.714G>A (p.Thr238=)	rs773030906	0.00003
NM_003722.5(TP63):c.992+8G>A	rs192488893	0.00003
NM_003722.5(TP63):c.156A>G (p.Pro52=)	rs780898702	0.00001
NM_003722.5(TP63):c.992+4A>C	rs534974406	0.00001
NM_003722.5(TP63):c.1350-6315C>A	rs1577182394
NM_003722.5(TP63):c.192-9_192-8del	rs794727498
NM_003722.5(TP63):c.20G>T (p.Arg7Leu)	rs568702479

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