Annotation Detail

Information
Associated Genes
GAA
Associated Variants
GAA p.Arg725Trp (p.R725W) ( ENST00000714058.1, ENST00000302262.8, ENST00000714055.1, ENST00000714057.1, ENST00000714054.1, ENST00000577106.6, ENST00000390015.7, ENST00000570803.6, ENST00000714062.1 )
GAA p.Arg725Trp (p.R725W) ( ENST00000302262.8, ENST00000390015.7, ENST00000570803.6, ENST00000577106.6, ENST00000714054.1, ENST00000714055.1, ENST00000714057.1, ENST00000714058.1, ENST00000714062.1 )
Associated Disease
Glycogen storage disease II, adult form
Source Database
ClinVar
Description
NM_000152.5(GAA):c.2173C>T (p.Arg725Trp) AND Glycogen storage disease II, adult form
ClinVar Allele ID
19063
ClinVar RefSeq Alternation Syntax
NM_001079803.3:c.2173C>T
ClinVar RefSeq Alternation Syntax
NM_001079804.3:c.2173C>T
ClinVar RefSeq Alternation Syntax
NM_000152.5:c.2173C>T
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
1993-01-01
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000004239
ClinVar Disease
Glycogen storage disease II, adult form
Observed Origin Sample
germline
Pubmed
8401535
Drugs