Annotation Detail
Information
- Associated Genes
- TTR
- Associated Variants
-
TTR p.Leu131Met (p.L131M)
(
ENST00000237014.8,
ENST00000610404.5,
ENST00000649620.1 )
TTR p.Leu131Met (p.L131M) ( ENST00000237014.8, ENST00000610404.5, ENST00000649620.1 ) - Associated Disease
- Familial amyloid neuropathy
- Source Database
- ClinVar
- Description
- NM_000371.4(TTR):c.391C>A (p.Leu131Met) AND Familial amyloid neuropathy
- ClinVar Allele ID
- 28463
- ClinVar RefSeq Alternation Syntax
- NM_000371.4:c.391C>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 1993-10-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000014366
- ClinVar Disease
- Familial amyloid neuropathy
- Observed Origin Sample
- germline
- Pubmed
- 8095302
- Pubmed
- 8406434
- Pubmed
- 1618497
- Pubmed
- 1626570
- Pubmed
- 13894830
Drugs