Is GAA p.Pro669= (c.2007C>T) pathogenic?

GAA p.Pro669= (c.2007C>T) is classified Likely benign in GAA (ClinVar, Single submitter, 1 submitter; last evaluated 2024-12-04). Ultra-rare (popmax 0.0144%, sas); Associated with glycogen storage disease II.

What condition is associated with GAA p.Pro669= (c.2007C>T)?

GAA p.Pro669= (c.2007C>T) is associated with glycogen storage disease II (ClinVar).

How common is GAA p.Pro669= (c.2007C>T) in the general population?

GAA p.Pro669= (c.2007C>T) is ultra-rare (popmax 0.0144%, sas) (gnomAD).

GAA p.Pro669=

Q: How is Glycogen storage disease due to acid maltase deficiency inherited?

Typically Autosomal recessive (Orphanet). A genetic counselor can assess individual risk for a family.

c.2007C>T · rs1343280702 · VCV2998469

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

ultra-rare (popmax 0.0144%, sas)

Conditions

glycogen storage disease II

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP -2.3	GERP -3.9
Overall
CADD	7.166	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0144% South Asian · 13/90,568 alleles

Filtering AF 0.00849% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00665%

Overall 0.000807% 13/1,611,112 alleles · ultra-rare exomes 13/1,458,820 · genomes 0/152,292 · joint denominator

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene: GAA
Protein: p.Pro669=
Coding: c.2007C>T
MANE Select: NM_000152
dbSNP: rs1343280702
Type: single nucleotide variant
Location: chr17:80112994 (GRCh38)
Gene constraint: LOEUF 1.008 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 92.32 · 19 PDB
Residue 669: a β-strand

Full GAA gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

glycogen storage disease II — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Glycogen storage disease due to acid maltase deficiency (Orphanet):

Inheritance: Autosomal recessive
Onset: Adolescent, Adult, Antenatal, Childhood, Infancy, Neonatal
Prevalence: 1-9 / 1 000 000 (Europe)

Similar variants

GAA p.Pro669Thr Uncertain significance ★★ ⚠ same residue
GAA p.Pro669Ala Uncertain significance ★ ⚠ same residue
GAA p.Pro669Leu Conflicting classifications of pathogenicity ★ ⚠ same residue
GAA p.Pro669_Phe670del Uncertain significance ★ same residue
GAA c.1076-1G>C Pathogenic ★★★ same condition
GAA c.1076-22T>G Pathogenic ★★★ same condition
GAA c.1194+5G>A Likely pathogenic ★★★ same condition
GAA c.1326+1G>A Pathogenic ★★★ same condition

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/gaa-p-pro669 (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown