The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries.
[Disclaimer]
- Gene obtained from curated document aligns with the Allele Registry but not with ClinVar data
- No CSPEC computer assertion could be determined for this classification!
Variant: NM_000152.5(GAA):c.2617dup (p.Tyr873fs)
CA658824790
550478 (ClinVar)
Gene: GAA
Condition: glycogen storage disease II
Inheritance Mode: Autosomal recessive inheritance
UUID: 300443cc-c894-4008-9935-4babb82a4986
Approved on: 2024-04-05
Published on: 2024-04-05
HGVS expressions
NM_000152.5:c.2617dup
NM_000152.5(GAA):c.2617dup (p.Tyr873fs)
NC_000017.11:g.80118328dup
CM000679.2:g.80118328dup
NC_000017.10:g.78092127dup
CM000679.1:g.78092127dup
NC_000017.9:g.75706722dup
NG_009822.1:g.21773dup
ENST00000570803.6:c.2617dup
ENST00000572080.2:c.*755dup
ENST00000577106.6:c.2617dup
ENST00000302262.8:c.2617dup
ENST00000302262.7:c.2617dup
ENST00000390015.7:c.2617dup
ENST00000573556.1:n.570dup
NM_000152.3:c.2617dup
NM_001079803.1:c.2617dup
NM_001079804.1:c.2617dup
NM_000152.4:c.2617dup
NM_001079803.2:c.2617dup
NM_001079804.2:c.2617dup
NM_001079803.3:c.2617dup
NM_001079804.3:c.2617dup
Evidence submitted by expert panel
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