Annotation Detail
Information
- Associated Genes
- TRPM4
- Associated Variants
-
TRPM4 p.Gly844Asp (p.G844D)
(
ENST00000252826.10,
ENST00000427978.6 )
TRPM4 p.Gly844Asp (p.G844D) ( ENST00000252826.10, ENST00000427978.6 ) - Associated Disease
- TRPM4-related disorder
- Source Database
- ClinVar
- Description
- NM_017636.4(TRPM4):c.2531G>A (p.Gly844Asp) AND TRPM4-related disorder
- ClinVar Allele ID
- 44162
- ClinVar RefSeq Alternation Syntax
- NM_001195227.2:c.2211-3540G>A
- ClinVar RefSeq Alternation Syntax
- NM_001321282.2:c.923G>A
- ClinVar RefSeq Alternation Syntax
- NM_001321281.2:c.2186G>A
- ClinVar RefSeq Alternation Syntax
- NM_001321285.2:c.1469G>A
- ClinVar RefSeq Alternation Syntax
- NM_017636.4:c.2531G>A
- ClinVar RefSeq Alternation Syntax
- NM_001321283.2:c.2009G>A
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2022-12-20
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004541017
- ClinVar Disease
- TRPM4-related disorder
- Observed Origin Sample
- germline
Drugs