Is ENG p.Pro225Arg (c.674C>G) pathogenic?

ENG p.Pro225Arg (c.674C>G) is classified Likely benign in ENG (ClinVar, Single submitter, 1 submitter; last evaluated 2024-01-16). AlphaMissense: likely benign (0.1759); Very rare (popmax 8.55e-05%, nfe); Associated with hereditary hemorrhagic telangiectasia.

What condition is associated with ENG p.Pro225Arg (c.674C>G)?

ENG p.Pro225Arg (c.674C>G) is associated with hereditary hemorrhagic telangiectasia (ClinVar).

How common is ENG p.Pro225Arg (c.674C>G) in the general population?

ENG p.Pro225Arg (c.674C>G) is very rare (popmax 8.55e-05%, nfe) (gnomAD).

How is Hereditary hemorrhagic telangiectasia inherited?

Typically Autosomal dominant (Orphanet). A genetic counselor can assess individual risk for a family.

What do computational predictors say about ENG p.Pro225Arg (c.674C>G)?

AlphaMissense predicts likely benign (score 0.1759) — an in-silico prediction, not a clinical call.

ENG p.Pro225Arg

c.674C>G · rs781715616 · VCV2723101

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.1759 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 8.55e-05%, nfe)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

hereditary hemorrhagic telangiectasia

Computational evidence

Protein change
AlphaMissense	0.1759	likely benign
REVEL	0.138	moderately benign-leaning
SaProt	LLR -8.66	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 9.2	GERP 1.9, phastCons 1
Regional constraint	o/e 0.86	unconstrained · MANE · 39 kb · p 5.2e-05 · regional, not allelic
Overall
CADD	25.4	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

Grpmax group 8.55e-05% European (non-Finnish) · 1/1,169,652 alleles

Overall 6.97e-05% 1/1,434,612 alleles · very rare

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: ENG
Protein: p.Pro225Arg
Coding: c.674C>G
MANE Select: NM_001114753
dbSNP: rs781715616
Type: single nucleotide variant
Location: chr9:127825710 (GRCh38)
Gene constraint: LOEUF 0.374 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 80.84 · 3 PDB
Residue 225: the 'required for interaction with gdf2' region; the 'or1, c-terminal part' region

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

Disease context

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

For Hereditary hemorrhagic telangiectasia (Orphanet):

Inheritance: Autosomal dominant
Onset: All ages
Prevalence: 1-5 / 10 000 (Europe)

Similar variants

ENG p.Pro225Leu Uncertain significance ★★ ⚠ same residue
ENG p.Pro225Thr Uncertain significance ★★ ⚠ same residue
ENG p.Pro225= Benign/Likely benign ★★ same residue
ENG p.Pro225Ala Uncertain significance ★ ⚠ same residue
ENG p.Pro225Gln Conflicting classifications of pathogenicity ★ ⚠ same residue
ENG p.Pro225fs Pathogenic ★★ same residue
ENG p.Pro225Ser Uncertain significance ★ ⚠ same residue
ENG p.Arg529His 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/eng-p-pro225arg (accessed [today's date]).

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