Annotation Detail
Information
- Associated Genes
- TP63
- Associated Variants
-
TP63 p.Cys561Gly (p.C561G)
(
ENST00000264731.8,
ENST00000320472.9,
ENST00000354600.10,
ENST00000392460.7,
ENST00000392461.7,
ENST00000392463.6,
ENST00000440651.6,
ENST00000449992.5,
ENST00000456148.1 )
TP63 p.Cys561Gly (p.C561G) ( ENST00000264731.8, ENST00000320472.9, ENST00000354600.10, ENST00000392460.7, ENST00000392461.7, ENST00000392463.6, ENST00000440651.6, ENST00000449992.5, ENST00000456148.1 ) - Associated Disease
- TP63-Related Spectrum Disorders
- Source Database
- ClinVar
- Description
- NM_003722.5(TP63):c.1681T>G (p.Cys561Gly) AND TP63-Related Spectrum Disorders
- ClinVar Allele ID
- 21575
- ClinVar RefSeq Alternation Syntax
- NM_001329144.2:c.1508-3389T>G
- ClinVar RefSeq Alternation Syntax
- NM_001114978.2:c.1652+1333T>G
- ClinVar RefSeq Alternation Syntax
- NM_001329148.2:c.1669T>G
- ClinVar RefSeq Alternation Syntax
- NM_001329145.2:c.1226-3389T>G
- ClinVar RefSeq Alternation Syntax
- NM_001329964.2:c.1675T>G
- ClinVar RefSeq Alternation Syntax
- NM_001329150.2:c.959-3389T>G
- ClinVar RefSeq Alternation Syntax
- NM_001114981.2:c.1370+1333T>G
- ClinVar RefSeq Alternation Syntax
- NM_001329149.2:c.1214-3389T>G
- ClinVar RefSeq Alternation Syntax
- NM_001329146.2:c.1144T>G
- ClinVar RefSeq Alternation Syntax
- NM_001114980.2:c.1399T>G
- ClinVar RefSeq Alternation Syntax
- NM_003722.5:c.1681T>G
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2019-01-25
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001067605
- ClinVar Disease
- TP63-Related Spectrum Disorders
- Observed Origin Sample
- germline
Drugs