Is CDH22 p.Arg368Ser (c.1102C>A) pathogenic?

CDH22 p.Arg368Ser (c.1102C>A) is classified Uncertain significance in CDH22 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-03-22). AlphaMissense: likely pathogenic (0.8249); Very rare (popmax 0.00448%, afr).

How common is CDH22 p.Arg368Ser (c.1102C>A) in the general population?

CDH22 p.Arg368Ser (c.1102C>A) is very rare (popmax 0.00448%, afr) (gnomAD).

What do computational predictors say about CDH22 p.Arg368Ser (c.1102C>A)?

AlphaMissense predicts likely pathogenic (score 0.8249) — an in-silico prediction, not a clinical call.

CDH22 p.Arg368Ser

c.1102C>A · VCV3998940

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.8249 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00448%, afr)

Missense predictors

2/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.8249	likely pathogenic
REVEL	0.219	benign-leaning
SaProt	LLR -10.13	damaging
⇒ AlphaMissense and SaProt call this damaging; REVEL does not.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 12	GERP 1.2, phastCons 1
Regional constraint	o/e 0.78	unconstrained · MANE · 76 kb · p 5.2e-13 · regional, not allelic
Overall
CADD	32.0	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00448% African / African-American · 3/67,036 alleles

Filtering AF 0.00233% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00206%

Overall 0.00272% 39/1,432,730 alleles · very rare

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.00448%	22,345
European (non-Finnish)	0.00321%	31,156
Remaining individualsnot grpmax-eligible	0.00185%	54,166

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: CDH22
Protein: p.Arg368Ser
Coding: c.1102C>A
MANE Select: NM_021248
Type: single nucleotide variant
Location: chr20:46210491 (GRCh38)
Gene constraint: LOEUF 0.782 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 76.19
Residue 368: the cadherin 3 domain

Full CDH22 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

CDH22 p.Ala782Val Benign ★★ same type
CDH22 p.Pro624= Benign ★★ same type
CDH22 p.Ala121Val Uncertain significance ★ ⚠ same type
CDH22 p.Ala15Pro Uncertain significance ★ ⚠ same type
CDH22 p.Ala19Thr Uncertain significance ★ ⚠ same type
CDH22 p.Ala384Thr Uncertain significance ★ ⚠ same type
CDH22 p.Ala39Val Uncertain significance ★ ⚠ same type
CDH22 p.Ala450Thr 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/cdh22-p-arg368ser (accessed [today's date]).

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