Is GAA p.Ser627= (c.1881C>T) pathogenic?

GAA p.Ser627= (c.1881C>T) is classified Likely benign in GAA (ClinVar, Multiple submitters, 3 submitters; last evaluated 2025-02-02). Ultra-rare (popmax 0.0112%, eas); Associated with Cardiovascular phenotype.

What condition is associated with GAA p.Ser627= (c.1881C>T)?

GAA p.Ser627= (c.1881C>T) is associated with Cardiovascular phenotype, glycogen storage disease II (ClinVar).

How common is GAA p.Ser627= (c.1881C>T) in the general population?

GAA p.Ser627= (c.1881C>T) is ultra-rare (popmax 0.0112%, eas) (gnomAD).

GAA p.Ser627=

c.1881C>T · rs779328815 · VCV992148

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 3 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0112%, eas)

Conditions

Cardiovascular phenotype

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 -15	GERP -2.7
Overall
CADD	0.365	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0112% East Asian · 5/44,668 alleles

Filtering AF 0.00436% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00277%

Overall 0.00112% 18/1,607,776 alleles · ultra-rare exomes 18/1,455,548 · genomes 0/152,228 · joint denominator

Ancestry group	Frequency	1 in
East Asiangrpmax	0.0112%	8,934
South Asian	0.00777%	12,872
European (non-Finnish)	0.000509%	196,314

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.Ser627=
Coding: c.1881C>T
MANE Select: NM_000152
dbSNP: rs779328815
Type: single nucleotide variant
Location: chr17:80112704 (GRCh38)
Gene constraint: LOEUF 1.008 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 92.32 · 19 PDB
Residue 627: a UniProt-annotated variant site (in iopd); an α-helix

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

Disease context

Cardiovascular phenotype — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: glycogen storage disease II

Similar variants

GAA p.Ser627Phe Pathogenic ★★★ same residue
GAA p.Ser627Cys Uncertain significance ★★ ⚠ same residue
GAA p.Ser627Pro Uncertain significance ★ ⚠ same residue
GAA p.Ser627del 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-ser627 (accessed [today's date]).

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