ClinVar for MedGen (Select 315656) - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1623182	NM_003722.5(TP63):c.654A>G (p.Pro218=)	TP63	Single nucleotide variant (synonymous variant)	TP63-Related Spectrum Disorders +7 more	GLikely benign
Select item 1601412	NM_003722.5(TP63):c.20G>T (p.Arg7Leu)	TP63 (R7L)	Single nucleotide variant (missense variant +1 more)	TP63-Related Spectrum Disorders +8 more	GBenign/Likely benign
Select item 1597542	NM_003722.5(TP63):c.156A>G (p.Pro52=)	TP63	Single nucleotide variant (synonymous variant)	TP63-Related Spectrum Disorders +7 more	GLikely benign
Select item 1595682	NM_003722.5(TP63):c.1575C>T (p.Leu525=)	TP63	Single nucleotide variant (synonymous variant +1 more)	TP63-Related Spectrum Disorders +7 more	GLikely benign
Select item 1535228	NM_003722.5(TP63):c.498C>T (p.Pro166=)	TP63	Single nucleotide variant (synonymous variant +1 more)	ADULT syndrome +7 more	GBenign/Likely benign
Select item 1522505	NM_003722.5(TP63):c.1394C>T (p.Pro465Leu)	TP63 (P286L +6 more)	Single nucleotide variant (missense variant)	ADULT syndrome +7 more	GUncertain significance
Select item 1510128	NM_003722.5(TP63):c.62G>A (p.Arg21His)	TP63 (R21H)	Single nucleotide variant (missense variant +1 more)	Rapp-Hodgkin syndrome +8 more	GUncertain significance
Select item 1503085	NM_003722.5(TP63):c.1352C>G (p.Thr451Ser)	TP63 (T447S +6 more)	Single nucleotide variant (missense variant)	Rapp-Hodgkin syndrome +7 more	GConflicting classifications of pathogenicity
Select item 1494162	NM_003722.5(TP63):c.1612A>G (p.Thr538Ala)	TP63 (T536A +4 more)	Single nucleotide variant (missense variant +1 more)	Rapp-Hodgkin syndrome +7 more	GUncertain significance
Select item 1476128	NM_003722.5(TP63):c.2003G>A (p.Arg668His)	TP63 (R666H +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	ADULT syndrome +7 more	GUncertain significance
Select item 1452532	NM_003722.5(TP63):c.1095G>A (p.Ser365=)	TP63	Single nucleotide variant (synonymous variant)	ADULT syndrome +7 more	GLikely benign
Select item 1436290	NM_003722.5(TP63):c.882+19A>T	TP63	Single nucleotide variant (intron variant)	TP63-Related Spectrum Disorders +7 more	GLikely benign
Select item 1433359	NM_003722.5(TP63):c.1807G>C (p.Asp603His)	TP63 (D599H +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	TP63-Related Spectrum Disorders +7 more	GUncertain significance
Select item 1421645	NM_003722.5(TP63):c.50C>G (p.Pro17Arg)	TP63 (P17R)	Single nucleotide variant (missense variant +1 more)	TP63-Related Spectrum Disorders +7 more	GUncertain significance
Select item 1412118	NM_003722.5(TP63):c.1814G>A (p.Arg605Gln)	TP63 (R601Q +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	TP63-Related Spectrum Disorders +8 more	GConflicting classifications of pathogenicity
Select item 1398414	NM_003722.5(TP63):c.110G>A (p.Arg37Gln)	TP63 (R35Q +1 more)	Single nucleotide variant (missense variant)	ADULT syndrome +7 more	GUncertain significance
Select item 1370657	NM_003722.5(TP63):c.1831TCC[1] (p.Ser612del)	TP63 (S518del +4 more)	Microsatellite (3 prime UTR variant +1 more)	ADULT syndrome +7 more	GUncertain significance
Select item 1333911	NM_003722.5(TP63):c.858dup (p.Leu287fs)	TP63 (L108fs +3 more)	Duplication (frameshift variant)	Rapp-Hodgkin syndrome	GLikely pathogenic
Select item 1314992	NM_003722.5(TP63):c.2021G>A (p.Arg674His)	TP63 (R495H +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +8 more	GUncertain significance
Select item 1110153	NM_003722.5(TP63):c.1626G>A (p.Pro542=)	TP63	Single nucleotide variant (synonymous variant +1 more)	ADULT syndrome +8 more	GLikely benign
Select item 1042494	NM_003722.5(TP63):c.1697C>T (p.Thr566Met)	TP63 (T564M +4 more)	Single nucleotide variant (missense variant +1 more)	ADULT syndrome +7 more	GUncertain significance
Select item 1038841	NM_003722.5(TP63):c.1121C>T (p.Thr374Met)	TP63 (T195M +3 more)	Single nucleotide variant (missense variant +1 more)	ADULT syndrome +7 more	GUncertain significance
Select item 807713	NM_003722.5(TP63):c.1790T>C (p.Ile597Thr)	TP63 (I593T +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Rapp-Hodgkin syndrome	GPathogenic
Select item 794734	NM_003722.5(TP63):c.992+8G>A	TP63	Single nucleotide variant (intron variant)	TP63-Related Spectrum Disorders +7 more	GLikely benign
Select item 779747	NM_003722.5(TP63):c.366G>A (p.Gln122=)	TP63	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GBenign/Likely benign
Select item 767371	NM_003722.5(TP63):c.1599C>T (p.Ser533=)	TP63	Single nucleotide variant (synonymous variant +1 more)	not provided +9 more	GLikely benign
Select item 707020	NM_003722.5(TP63):c.1788G>A (p.Ala596=)	TP63	Single nucleotide variant (3 prime UTR variant +1 more)	TP63-related disorder +8 more	GBenign/Likely benign
Select item 706677	NM_003722.5(TP63):c.714G>A (p.Thr238=)	TP63	Single nucleotide variant (synonymous variant)	not provided +7 more	GLikely benign
Select item 706674	NM_003722.5(TP63):c.402T>C (p.Tyr134=)	TP63	Single nucleotide variant (synonymous variant +1 more)	TP63-Related Spectrum Disorders +7 more	GLikely benign
Select item 596662	NM_003722.5(TP63):c.290G>A (p.Arg97His)	TP63 (R97H +1 more)	Single nucleotide variant (missense variant)	TP63-Related Spectrum Disorders +8 more	GUncertain significance
Select item 344386	NM_003722.5(TP63):c.992+4A>C	TP63	Single nucleotide variant (intron variant)	ADULT syndrome +8 more	GBenign/Likely benign
Select item 286990	NM_003722.5(TP63):c.1531C>A (p.Pro511Thr)	TP63 (P511T +4 more)	Single nucleotide variant (missense variant +1 more)	Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 +9 more	GBenign/Likely benign
Select item 196365	NM_003722.5(TP63):c.192-9_192-8del	TP63	Deletion (intron variant)	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome +9 more	GBenign/Likely benign
Select item 69817	NM_003722.5(TP63):c.1825G>A (p.Glu609Lys)	TP63 (E609K +4 more)	Single nucleotide variant (3 prime UTR variant +1 more)	ADULT syndrome +6 more	GUncertain significance
Select item 6553	NM_003722.5(TP63):c.1833_1843dup (p.His615fs)	TP63 (H436fs +4 more)	Duplication (3 prime UTR variant +1 more)	Rapp-Hodgkin syndrome +1 more	GPathogenic
Select item 6551	NM_003722.5(TP63):c.1900del (p.Arg634fs)	TP63 (R455fs +4 more)	Deletion (3 prime UTR variant +1 more)	Rapp-Hodgkin syndrome	GPathogenic
Select item 6545	NM_003722.5(TP63):c.1738T>C (p.Ser580Pro)	TP63 (S580P +4 more)	Single nucleotide variant (missense variant +1 more)	Rapp-Hodgkin syndrome	GPathogenic
Select item 6544	NM_003722.5(TP63):c.1646T>C (p.Ile549Thr)	TP63 (I549T +4 more)	Single nucleotide variant (missense variant +1 more)	Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome +1 more	GPathogenic
Select item 6543	NM_003722.5(TP63):c.1976del (p.Asn659fs)	TP63 (N480fs +4 more)	Deletion (3 prime UTR variant +1 more)	Rapp-Hodgkin syndrome	GPathogenic
Select item 6542	NM_003722.5(TP63):c.1827del (p.Glu609fs)	TP63 (E430fs +4 more)	Deletion (3 prime UTR variant +1 more)	Rapp-Hodgkin syndrome	GPathogenic
Select item 6533	NM_003722.5(TP63):c.953G>A (p.Arg318His)	TP63 (R318H +3 more)	Single nucleotide variant (missense variant)	Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 +2 more	GPathogenic/Likely pathogenic
Select item 6527	NM_003722.5(TP63):c.727C>T (p.Arg243Trp)	TP63 (R243W +3 more)	Single nucleotide variant (missense variant)	Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 +3 more	GPathogenic

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Items: 42