Annotation Detail
Information
- Associated Genes
- TTR
- Associated Variants
-
TTR p.Ile127Val (p.I127V)
(
ENST00000237014.8,
ENST00000610404.5,
ENST00000649620.1 )
TTR p.Ile127Val (p.I127V) ( ENST00000237014.8, ENST00000649620.1, ENST00000610404.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000371.4(TTR):c.379A>G (p.Ile127Val) AND not provided
- ClinVar Allele ID
- 28489
- ClinVar RefSeq Alternation Syntax
- NM_000371.4:c.379A>G
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2023-10-01
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001090344
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs