Annotation Detail
Information
- Associated Genes
- GAA
- Associated Variants
-
GAA p.Trp376CysfsTer16 (p.W376Cfs*16)
(
ENST00000714058.1,
ENST00000714055.1,
ENST00000302262.8,
ENST00000570803.6,
ENST00000390015.7,
ENST00000714062.1,
ENST00000714057.1,
ENST00000714054.1,
ENST00000577106.6 )
GAA p.Trp376CysfsTer16 (p.W376Cfs*16) ( ENST00000302262.8, ENST00000390015.7, ENST00000570803.6, ENST00000577106.6, ENST00000714054.1, ENST00000714055.1, ENST00000714057.1, ENST00000714058.1, ENST00000714062.1 ) - Associated Disease
- Glycogen storage disease, type II
- Source Database
- ClinVar
- Description
- NM_000152.5(GAA):c.1128_1129delinsC (p.Trp376fs) AND Glycogen storage disease, type II
- ClinVar Allele ID
- 186999
- ClinVar RefSeq Alternation Syntax
- NM_000152.5:c.1128_1129delinsC
- ClinVar RefSeq Alternation Syntax
- NM_001079803.3:c.1128_1129delinsC
- ClinVar RefSeq Alternation Syntax
- NM_001079804.3:c.1128_1129delinsC
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2020-02-14
- Clinical Significance Review Status
- reviewed by expert panel
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000169433
- ClinVar Disease
- Glycogen storage disease, type II
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs