NM_000152.5(GAA):c.711G>A (p.Ala237=) AND Glycogen storage disease, type II
- Germline classification:
- Conflicting interpretations of pathogenicity (4 submissions)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000530651.18
Allele description [Variation Report for NM_000152.5(GAA):c.711G>A (p.Ala237=)]
NM_000152.5(GAA):c.711G>A (p.Ala237=)
Condition(s)
- Name:
- Glycogen storage disease, type II (GSD2)
- Synonyms:
- ACID ALPHA-GLUCOSIDASE DEFICIENCY; GLYCOGENOSIS, GENERALIZED, CARDIAC FORM; GSD II; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009290; MedGen: C0017921; Orphanet: 365; OMIM: 232300
-
601077149F1 NIH_MGC_12 Homo sapiens cDNA clone IMAGE:3462829 5', mRNA sequence
601077149F1 NIH_MGC_12 Homo sapiens cDNA clone IMAGE:3462829 5', mRNA sequencegi|9777599|gnl|dbEST|5726330|gb|BE5 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024