Is PDE3B p.Arg725His (c.2174G>A) pathogenic?

PDE3B p.Arg725His (c.2174G>A) is classified Uncertain significance in PDE3B (ClinVar, Single submitter, 1 submitter; last evaluated 2025-05-21). AlphaMissense: likely benign (0.0637); Very rare (popmax 0.00697%, afr).

How common is PDE3B p.Arg725His (c.2174G>A) in the general population?

PDE3B p.Arg725His (c.2174G>A) is very rare (popmax 0.00697%, afr) (gnomAD).

What do computational predictors say about PDE3B p.Arg725His (c.2174G>A)?

AlphaMissense predicts likely benign (score 0.0637) — an in-silico prediction, not a clinical call.

PDE3B p.Arg725His

c.2174G>A · VCV3930031

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.0637 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00697%, afr)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.0637	likely benign
REVEL	0.1	moderately benign-leaning
SaProt	LLR -5.86	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 -0.51	GERP -0.86
Regional constraint	o/e 0.76	unconstrained · MANE · 39 kb · p 1.8e-08 · regional, not allelic
Overall
CADD	17.35	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification

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

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00697% African / African-American · 5/71,690 alleles

Filtering AF 0.00274% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00178%

Overall 0.00131% 20/1,521,946 alleles · very rare

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.00697%	14,338
Admixed American	0.00181%	55,380
European (non-Finnish)	0.00126%	79,202

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: PDE3B
Protein: p.Arg725His
Coding: c.2174G>A
MANE Select: NM_000922
Type: single nucleotide variant
Location: chr11:14832801 (GRCh38)
Gene constraint: LOEUF 0.955 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 64.10 · 4 PDB
Residue 725: an α-helix; the pdease domain

Full PDE3B gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

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CYP2R1 p.His381Arg Uncertain significance ★★ ⚠ same type
CYP2R1 p.Ile332Thr Uncertain significance ★★ ⚠ same type
CYP2R1 p.Met284Ile Uncertain significance ★★ ⚠ same type
CYP2R1 p.Pro36Leu Uncertain significance ★★ ⚠ same type
CYP2R1 p.Tyr431His Uncertain significance ★★ ⚠ same type
PDE3B p.Thr137Ala 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/pde3b-p-arg725his (accessed [today's date]).

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