Annotation Detail
Information
- Associated Genes
- CASR
- Associated Variants
-
CASR p.Phe798Cys (p.F798C)
(
ENST00000498619.4,
ENST00000490131.7,
ENST00000638421.1,
ENST00000639785.2 )
CASR p.Phe798Cys (p.F798C) ( ENST00000490131.7, ENST00000498619.4, ENST00000638421.1, ENST00000639785.2 ) - Associated Disease
- autosomal dominant hypocalcemia 1
- Source Database
- ClinVar
- Description
- NM_000388.4(CASR):c.2363T>G (p.Phe788Cys) AND Autosomal dominant hypocalcemia 1
- ClinVar Allele ID
- 23375
- ClinVar RefSeq Alternation Syntax
- NM_001178065.2:c.2393T>G
- ClinVar RefSeq Alternation Syntax
- NM_000388.4:c.2363T>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2018-07-18
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000008838
- ClinVar Disease
- Autosomal dominant hypocalcemia 1
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
- Pubmed
- 9661634
Drugs