Is GUCY2C p.Ser92= (c.276A>G) pathogenic?

GUCY2C p.Ser92= (c.276A>G) is classified Likely benign in GUCY2C (ClinVar, Single submitter, 1 submitter; last evaluated 2025-01-27). Very rare (popmax 0.00267%, afr).

How common is GUCY2C p.Ser92= (c.276A>G) in the general population?

GUCY2C p.Ser92= (c.276A>G) is very rare (popmax 0.00267%, afr) (gnomAD).

GUCY2C p.Ser92=

c.276A>G · rs766954517 · VCV2959671

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00267%, afr)

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 -0.16	GERP -3.4, phastCons 0.56
Overall
CADD	5.088	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00267% African / African-American · 2/74,926 alleles

Filtering AF 0.000689% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000539%

Overall 0.00105% 17/1,613,718 alleles · very rare exomes 15/1,461,492 · genomes 2/152,226 · joint denominator

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.00267%	37,463
Remaining individualsnot grpmax-eligible	0.0016%	62,482
European (non-Finnish)	0.00119%	84,264

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: GUCY2C
Protein: p.Ser92=
Coding: c.276A>G
MANE Select: NM_004963
dbSNP: rs766954517
Type: single nucleotide variant
Location: chr12:14688005 (GRCh38)
Gene constraint: LOEUF 1.118 · pLI <0.01 · ClinGen HI 0/3 (gnomAD)
Structure: AlphaFold pLDDT 80.08 · 3 PDB

Full GUCY2C gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

GUCY2C p.Asp387Gly Pathogenic ★★ ⚠ same type
GUCY2C c.2602-1G>C Uncertain significance ★★ same type
GUCY2C c.2776+5G>A Uncertain significance ★★ same type
GUCY2C c.612-1G>A Uncertain significance ★★ same type
GUCY2C p.Ala450Thr Uncertain significance ★★ ⚠ same type
GUCY2C p.Ala48Gly Uncertain significance ★★ ⚠ same type
GUCY2C p.Ala670Thr Uncertain significance ★★ ⚠ same type
GUCY2C p.Ala897Thr Uncertain significance ★★ ⚠ same type

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/gucy2c-p-ser92 (accessed [today's date]).

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