Is APC p.Ala2121Pro (c.6361G>C) pathogenic?

APC p.Ala2121Pro (c.6361G>C) is classified Uncertain significance in APC (ClinVar, Multiple submitters, 5 submitters; last evaluated 2024-05-24). AlphaMissense: likely pathogenic (0.7398); Absent from gnomAD v4.1; Associated with hereditary neoplastic syndrome.

What condition is associated with APC p.Ala2121Pro (c.6361G>C)?

APC p.Ala2121Pro (c.6361G>C) is associated with hereditary neoplastic syndrome, familial adenomatous polyposis 1 (ClinVar).

How common is APC p.Ala2121Pro (c.6361G>C) in the general population?

APC p.Ala2121Pro (c.6361G>C) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about APC p.Ala2121Pro (c.6361G>C)?

AlphaMissense predicts likely pathogenic (score 0.7398) — an in-silico prediction, not a clinical call.

APC p.Ala2121Pro

c.6361G>C · rs1561606746 · VCV619775

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 5 submitters

AlphaMissense

likely pathogenic

0.7398 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
AlphaMissense	0.7398	likely pathogenic
REVEL	0.613	indeterminate
SaProt	—	not scored · why
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 12	GERP 2.8, phastCons 1
Regional constraint	o/e 1.08	unconstrained · MANE · 4,236 bp · p 0.00065 · regional, not allelic
Overall
CADD	27.2	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL is an independent agreement signal.

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: APC
Protein: p.Ala2121Pro
Coding: c.6361G>C
MANE Select: NM_000038
dbSNP: rs1561606746
Type: single nucleotide variant
Location: chr5:112841955 (GRCh38)
Gene constraint: LOEUF 0.321 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)

Full APC 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

Also linked: familial adenomatous polyposis 1

Similar variants

APC p.Ala2121Thr Uncertain significance ★★ same residue
APC p.Ala2121= Likely benign ★★ same residue
APC p.Ala2121Gly Uncertain significance ★ same residue
APC p.Ala2121_Ala2122dup Uncertain significance ★★ same residue
APC p.Ala2121fs Pathogenic ★ same residue
APC c.1312+3A>C Likely pathogenic ★★★ same condition
APC c.1312+3A>G Pathogenic ★★★ same condition
APC c.1312+5G>A Likely 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/apc-p-ala2121pro (accessed [today's date]).

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