Annotation Detail
Information
- Associated Genes
- TTR
- Associated Variants
-
TTR p.Ala117Gly (p.A117G)
(
ENST00000237014.8,
ENST00000610404.5,
ENST00000649620.1 )
TTR p.Ala117Gly (p.A117G) ( ENST00000237014.8, ENST00000610404.5, ENST00000649620.1 ) - Associated Disease
- Familial amyloid neuropathy
- Source Database
- ClinVar
- Description
- NM_000371.4(TTR):c.350C>G (p.Ala117Gly) AND Familial amyloid neuropathy
- ClinVar Allele ID
- 28487
- ClinVar RefSeq Alternation Syntax
- NM_000371.4:c.350C>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 1994-01-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000014390
- ClinVar Disease
- Familial amyloid neuropathy
- Observed Origin Sample
- unknown
- Pubmed
- 8133316
Drugs