Annotation Detail
Information
- Associated Genes
- GAA
- Associated Variants
-
GAA p.Arg672Trp (p.R672W)
(
ENST00000570803.6,
ENST00000390015.7,
ENST00000714062.1,
ENST00000714057.1,
ENST00000577106.6,
ENST00000714054.1,
ENST00000714055.1,
ENST00000302262.8,
ENST00000714058.1 )
GAA p.Arg672Trp (p.R672W) ( ENST00000302262.8, ENST00000390015.7, ENST00000570803.6, ENST00000577106.6, ENST00000714054.1, ENST00000714055.1, ENST00000714057.1, ENST00000714058.1, ENST00000714062.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000152.5(GAA):c.2014C>T (p.Arg672Trp) AND not provided
- ClinVar Allele ID
- 187014
- ClinVar RefSeq Alternation Syntax
- NM_001079803.3:c.2014C>T
- ClinVar RefSeq Alternation Syntax
- NM_001079804.3:c.2014C>T
- ClinVar RefSeq Alternation Syntax
- NM_000152.5:c.2014C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-12-18
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000725325
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs