Annotation Detail

Information
Associated Genes
TP63
Associated Variants
TP63 p.Asp351Gly (p.D351G) ( ENST00000264731.8, ENST00000320472.9, ENST00000354600.10, ENST00000392460.7, ENST00000392461.7, ENST00000392463.6, ENST00000418709.6, ENST00000437221.5, ENST00000440651.6, ENST00000449992.5, ENST00000456148.1 )
TP63 p.Asp351Gly (p.D351G) ( ENST00000264731.8, ENST00000320472.9, ENST00000354600.10, ENST00000392460.7, ENST00000392461.7, ENST00000392463.6, ENST00000418709.6, ENST00000437221.5, ENST00000440651.6, ENST00000449992.5, ENST00000456148.1 )
Associated Disease
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3
Source Database
ClinVar
Description
NM_003722.5(TP63):c.1052A>G (p.Asp351Gly) AND Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3
ClinVar Allele ID
21580
ClinVar RefSeq Alternation Syntax
NM_001329148.2:c.1052A>G
ClinVar RefSeq Alternation Syntax
NM_001114982.2:c.770A>G
ClinVar RefSeq Alternation Syntax
NM_001329145.2:c.770A>G
ClinVar RefSeq Alternation Syntax
NM_001329146.2:c.515A>G
ClinVar RefSeq Alternation Syntax
NM_001329964.2:c.1046A>G
ClinVar RefSeq Alternation Syntax
NM_001114978.2:c.1052A>G
ClinVar RefSeq Alternation Syntax
NM_001114980.2:c.770A>G
ClinVar RefSeq Alternation Syntax
NM_001114979.2:c.1052A>G
ClinVar RefSeq Alternation Syntax
NM_001329150.2:c.515A>G
ClinVar RefSeq Alternation Syntax
NM_003722.5:c.1052A>G
ClinVar RefSeq Alternation Syntax
NM_001329149.2:c.770A>G
ClinVar RefSeq Alternation Syntax
NM_001114981.2:c.770A>G
ClinVar RefSeq Alternation Syntax
NM_001329144.2:c.1052A>G
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2003-07-30
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000006915
ClinVar Disease
Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3
Observed Origin Sample
germline
Pubmed
10936828
Pubmed
12838557
Pubmed
9028452
Drugs