Is APC2 p.Arg2058Pro (c.6173G>C) pathogenic?

APC2 p.Arg2058Pro (c.6173G>C) is classified Likely benign in APC2 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-10-07). AlphaMissense: likely benign (0.057); Very rare (popmax 0.00716%, sas); Associated with Inborn genetic diseases.

What condition is associated with APC2 p.Arg2058Pro (c.6173G>C)?

APC2 p.Arg2058Pro (c.6173G>C) is associated with Inborn genetic diseases (ClinVar).

How common is APC2 p.Arg2058Pro (c.6173G>C) in the general population?

APC2 p.Arg2058Pro (c.6173G>C) is very rare (popmax 0.00716%, sas) (gnomAD).

What do computational predictors say about APC2 p.Arg2058Pro (c.6173G>C)?

AlphaMissense predicts likely benign (score 0.057) — an in-silico prediction, not a clinical call.

APC2 p.Arg2058Pro

c.6173G>C · VCV4582792

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.057 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00716%, sas)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.057	likely benign
REVEL	0.16	moderately benign-leaning
SaProt	LLR -5.45	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 0.66	GERP -1.4
Overall
CADD	9.795	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 0.00716% South Asian · 2/27,938 alleles

Filtering AF 0.00187% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00158%

Overall 0.00251% 28/1,116,564 alleles · very rare exomes 26/968,700 · genomes 2/147,864 · joint denominator

Ancestry group	Frequency	1 in
South Asiangrpmax	0.00716%	13,969
European (non-Finnish)	0.00272%	36,737
Remaining individualsnot grpmax-eligible	0.00271%	36,872

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: APC2
Protein: p.Arg2058Pro
Coding: c.6173G>C
MANE Select: NM_005883
Type: single nucleotide variant
Location: chr19:1469474 (GRCh38)
Gene constraint: LOEUF 0.961 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 48.87
Residue 2058: the 'disordered' region; a UniProt-annotated variant site (in cdcbm10)

Full APC2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

APC2 p.Ala1059Glu Uncertain significance ★★ ⚠ same condition
APC2 p.Ala1103Thr Uncertain significance ★★ ⚠ same condition
APC2 p.Ala1116Val Uncertain significance ★★ ⚠ same condition
APC2 p.Ala126Ser Uncertain significance ★★ ⚠ same condition
APC2 p.Ala1311Thr Uncertain significance ★★ ⚠ same condition
APC2 p.Ala1359Val Uncertain significance ★★ ⚠ same condition
APC2 p.Ala1438Thr Uncertain significance ★★ ⚠ same condition
APC2 p.Ala1492Glu Uncertain significance ★★ ⚠ 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/apc2-p-arg2058pro (accessed [today's date]).

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