List of variants in gene TP63 reported as likely benign by Illumina Laboratory Services, Illumina

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_003722.5(TP63):c.*2636del	rs5855278	0.03709
NM_003722.5(TP63):c.1652+14A>C	rs150685395	0.01158
NM_003722.5(TP63):c.*1620T>C	rs34328757	0.00869
NM_003722.5(TP63):c.*1343T>C	rs35659283	0.00640
NM_003722.5(TP63):c.*2139G>A	rs35356690	0.00627
NM_003722.5(TP63):c.*2016A>G	rs115660354	0.00499
NM_003722.5(TP63):c.*2002T>G	rs35969817	0.00439
NM_003722.5(TP63):c.*854A>G	rs187751631	0.00427
NM_003722.5(TP63):c.1531C>A (p.Pro511Thr)	rs148076109	0.00295
NM_003722.5(TP63):c.399C>T (p.Pro133=)	rs145730343	0.00196
NM_003722.5(TP63):c.*2477T>G	rs186295449	0.00187
NM_003722.5(TP63):c.*2123C>T	rs36064124	0.00159
NM_003722.5(TP63):c.1587C>T (p.Leu529=)	rs141847552	0.00082
NM_003722.5(TP63):c.*627T>C	rs184452906	0.00043
NM_003722.5(TP63):c.*2625A>T	rs35694511	0.00026
NM_003722.5(TP63):c.699A>G (p.Lys233=)	rs199727371	0.00011
NM_003722.5(TP63):c.*2318G>A	rs199834330	0.00009
NM_003722.5(TP63):c.84T>G (p.His28Gln)	rs370716448	0.00009
NM_003722.5(TP63):c.*379T>A	rs192879052	0.00006
NM_003722.5(TP63):c.1707G>A (p.Gly569=)	rs202009057	0.00006
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.*1464G>T	rs571277874	0.00003
NM_003722.5(TP63):c.992+4A>C	rs534974406	0.00001
NM_003722.5(TP63):c.2719_2720del	rs574327104
NM_003722.5(TP63):c.*471A>T	rs144018872

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