Annotation Detail
Information
- Associated Genes
- LMNA
- Associated Variants
-
LMNA p.Arg584His (p.R584H)
(
ENST00000361308.9,
ENST00000368299.7,
ENST00000504687.7,
ENST00000368300.9,
ENST00000682650.1,
ENST00000676385.2,
ENST00000448611.6,
ENST00000675667.1,
ENST00000675939.1,
ENST00000473598.6,
ENST00000683032.1 )
LMNA p.Arg584His (p.R584H) ( ENST00000361308.9, ENST00000368299.7, ENST00000368300.9, ENST00000448611.6, ENST00000473598.6, ENST00000504687.7, ENST00000675667.1, ENST00000675939.1, ENST00000676385.2, ENST00000682650.1, ENST00000683032.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_170707.4(LMNA):c.1751G>A (p.Arg584His) AND not specified
- ClinVar Allele ID
- 57213
- ClinVar RefSeq Alternation Syntax
- NM_170708.4:c.1661G>A
- ClinVar RefSeq Alternation Syntax
- NM_001257374.3:c.1415G>A
- ClinVar RefSeq Alternation Syntax
- NM_001282626.2:c.1751G>A
- ClinVar RefSeq Alternation Syntax
- NM_170707.4:c.1751G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2019-06-28
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000041330
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs