Annotation Detail
Information
- Associated Genes
- LMNA
- Associated Variants
-
LMNA c.1968+5G>A
(
ENST00000368299.7,
ENST00000361308.9,
ENST00000368300.9,
ENST00000682650.1,
ENST00000504687.7,
ENST00000676385.2,
ENST00000448611.6,
ENST00000675667.1,
ENST00000675939.1,
ENST00000683032.1,
ENST00000473598.6 )
LMNA c.1968+5G>A ( ENST00000361308.9, ENST00000368299.7, ENST00000368300.9, ENST00000448611.6, ENST00000473598.6, ENST00000504687.7, ENST00000675667.1, ENST00000675939.1, ENST00000676385.2, ENST00000682650.1, ENST00000683032.1 ) - Associated Disease
- Hutchinson-Gilford progeria syndrome, atypical
- Source Database
- ClinVar
- Description
- NM_170707.4(LMNA):c.1968+5G>A AND Hutchinson-Gilford progeria syndrome, atypical
- ClinVar Allele ID
- 172117
- ClinVar RefSeq Alternation Syntax
- NM_001257374.3:c.1632+5G>A
- ClinVar RefSeq Alternation Syntax
- NM_170707.4:c.1968+5G>A
- ClinVar RefSeq Alternation Syntax
- NM_170708.4:c.1878+5G>A
- ClinVar RefSeq Alternation Syntax
- NM_001282626.2:c.1818+155G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2015-08-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000190823
- ClinVar Disease
- Hutchinson-Gilford progeria syndrome, atypical
- Observed Origin Sample
- germline
- Pubmed
- 22065502
- Pubmed
- 15317753
- Pubmed
- 25649378
Drugs