Is CDH1 p.Ala275Ser (c.823G>T) pathogenic?

CDH1 p.Ala275Ser (c.823G>T) is classified Likely benign in CDH1 (ClinVar, Single submitter, 1 submitter; last evaluated 2026-05-11). AlphaMissense: likely benign (0.1136); Absent from gnomAD v4.1; Associated with hereditary neoplastic syndrome.

What condition is associated with CDH1 p.Ala275Ser (c.823G>T)?

CDH1 p.Ala275Ser (c.823G>T) is associated with hereditary neoplastic syndrome (ClinVar).

How common is CDH1 p.Ala275Ser (c.823G>T) in the general population?

CDH1 p.Ala275Ser (c.823G>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about CDH1 p.Ala275Ser (c.823G>T)?

AlphaMissense predicts likely benign (score 0.1136) — an in-silico prediction, not a clinical call.

CDH1 p.Ala275Ser

c.823G>T · rs1597892587 · VCV1762585

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.1136 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
AlphaMissense	0.1136	likely benign
REVEL	0.091	moderately benign-leaning
SaProt	LLR -6.59	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	<0.2	all four deltas below 0.2 · G>A here scores Δ0.82 · evaluated, not missing
Constraint at this position
Conservation	phyloP 8.5	GERP 1.8, phastCons 1
Regional constraint	o/e 0.87	unconstrained · MANE · 25 kb · p 0.00015 · regional, not allelic
Overall
CADD	20.4	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

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: CDH1
Protein: p.Ala275Ser
Coding: c.823G>T
MANE Select: NM_004360
dbSNP: rs1597892587
Type: single nucleotide variant
Location: chr16:68810332 (GRCh38)
Gene constraint: LOEUF 0.514 · pLI 0.86 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 79.13 · 22 PDB
Residue 275: the cadherin 2 domain; a UniProt-annotated variant site (found in gastric carcinoma cell lines)

Full CDH1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

hereditary neoplastic syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

CDH1 p.Ala275Thr Uncertain significance ★ ⚠ same residue
CDH1 p.Ala275Val Conflicting classifications of pathogenicity ★ ⚠ same residue
CDH1 p.Ala275Asp Uncertain significance ★ ⚠ same residue
CDH1 p.Ala275= Benign ★ same residue
CDH1 c.1008+2T>C Likely pathogenic ★★★ same condition
CDH1 c.1137+1G>A Pathogenic ★★★ same condition
CDH1 c.1137+2T>C Likely pathogenic ★★★ same condition
CDH1 c.1565+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/cdh1-p-ala275ser (accessed [today's date]).

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