Annotation Detail
Information
- Associated Genes
- CASR
- Associated Variants
-
CASR p.Gln691His (p.Q691H)
(
ENST00000490131.7,
ENST00000498619.4,
ENST00000638421.1,
ENST00000639785.2 )
CASR p.Gln691His (p.Q691H) ( ENST00000490131.7, ENST00000498619.4, ENST00000638421.1, ENST00000639785.2 ) - Associated Disease
- autosomal dominant hypocalcemia 1
- Source Database
- ClinVar
- Description
- NM_000388.4(CASR):c.2043G>T (p.Gln681His) AND Autosomal dominant hypocalcemia 1
- ClinVar Allele ID
- 23359
- ClinVar RefSeq Alternation Syntax
- NM_000388.4:c.2043G>T
- ClinVar RefSeq Alternation Syntax
- NM_001178065.2:c.2073G>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 1996-05-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000008821
- ClinVar Disease
- Autosomal dominant hypocalcemia 1
- Observed Origin Sample
- germline
- Pubmed
- 8733126
Drugs