Annotation Detail
Information
- Associated Genes
- LMNA
- Associated Variants
-
LMNA p.Ser636= (p.S636=)
(
ENST00000683032.1,
ENST00000473598.6,
ENST00000675667.1,
ENST00000675939.1,
ENST00000448611.6,
ENST00000504687.7,
ENST00000368300.9,
ENST00000682650.1,
ENST00000676385.2,
ENST00000368299.7,
ENST00000361308.9 )
LMNA p.Ser636= (p.S636=) ( ENST00000361308.9, ENST00000368299.7, ENST00000368300.9, ENST00000448611.6, ENST00000473598.6, ENST00000504687.7, ENST00000675667.1, ENST00000675939.1, ENST00000676385.2, ENST00000682650.1, ENST00000683032.1 ) - Associated Disease
- cardiomyopathy
- Source Database
- ClinVar
- Description
- NM_170707.4(LMNA):c.1908C>T (p.Ser636=) AND Cardiomyopathy
- ClinVar Allele ID
- 77772
- ClinVar RefSeq Alternation Syntax
- NM_170707.4:c.1908C>T
- ClinVar RefSeq Alternation Syntax
- NM_001282626.2:c.1818+90C>T
- ClinVar RefSeq Alternation Syntax
- NM_001257374.3:c.1572C>T
- ClinVar RefSeq Alternation Syntax
- NM_170708.4:c.1818C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2023-10-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003531949
- ClinVar Disease
- Cardiomyopathy
- Observed Origin Sample
- germline
Drugs