Annotation Detail
Information
- Associated Genes
- CASP10
- Associated Variants
-
CASP10 p.Ser59= (p.S59=)
(
ENST00000471191.2,
ENST00000286186.11,
ENST00000272879.9,
ENST00000313728.12,
ENST00000374650.8,
ENST00000346817.10,
ENST00000448480.1,
ENST00000696199.1 )
CASP10 p.Ser59= (p.S59=) ( ENST00000272879.9, ENST00000286186.11, ENST00000313728.12, ENST00000346817.10, ENST00000374650.8, ENST00000448480.1, ENST00000471191.2, ENST00000696199.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_032977.4(CASP10):c.177A>G (p.Ser59=) AND not specified
- ClinVar Allele ID
- 284490
- ClinVar RefSeq Alternation Syntax
- NM_001206542.2:c.177A>G
- ClinVar RefSeq Alternation Syntax
- NM_032974.5:c.177A>G
- ClinVar RefSeq Alternation Syntax
- NM_001206524.2:c.177A>G
- ClinVar RefSeq Alternation Syntax
- NM_032976.4:c.177A>G
- ClinVar RefSeq Alternation Syntax
- NM_032977.4:c.177A>G
- ClinVar RefSeq Alternation Syntax
- NM_001230.5:c.177A>G
- ClinVar RefSeq Alternation Syntax
- NM_001306083.2:c.177A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2023-11-12
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000454697
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs