Is ENTREP1 p.Ala588Val (c.1763C>T) pathogenic?

ENTREP1 p.Ala588Val (c.1763C>T) is classified Conflicting classifications of pathogenicity in ENTREP1 (ClinVar, Conflicting submitters, 2 submitters; last evaluated 2025-08-04). AlphaMissense: likely benign (0.0923); Rare (popmax 0.569%, afr).

How common is ENTREP1 p.Ala588Val (c.1763C>T) in the general population?

ENTREP1 p.Ala588Val (c.1763C>T) is rare (popmax 0.569%, afr) (gnomAD).

What do computational predictors say about ENTREP1 p.Ala588Val (c.1763C>T)?

AlphaMissense predicts likely benign (score 0.0923) — an in-silico prediction, not a clinical call.

ENTREP1 p.Ala588Val

c.1763C>T · rs145135759 · VCV514986

Conflicting classifications of pathogenicity Conflicting submitters

Classification

Conflicting classifications of pathogenicity

ClinVar

Review

Conflicting submitters ★☆☆☆

ClinVar · 2 submitters

AlphaMissense

likely benign

0.0923 · ACMG-weighted

gnomAD v4.1

Rare

rare (popmax 0.569%, afr)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.0923	likely benign
REVEL	0.054	moderately benign-leaning
SaProt	LLR -6.73	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 4.9	GERP 0.62, phastCons 1
Regional constraint	o/e 0.98	unconstrained · MANE · 7,796 bp · p 0.71 · regional, not allelic
Overall
CADD	20.7	PHRED · no single calibrated threshold — expert panels disagree

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

⚠ Isoform check: AlphaMissense numbered on a different transcript (AM A435V vs ClinVar A588V) — verify the residue.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.569% African / African-American · 427/75,054 alleles

Filtering AF 0.524% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.507%

Overall 0.03% 484/1,613,430 alleles · rare

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.569%	176
Remaining individualsnot grpmax-eligible	0.0433%	2,312
Admixed American	0.0334%	2,997
European (non-Finnish)	0.000848%	117,976

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: ENTREP1
Protein: p.Ala588Val
Coding: c.1763C>T
MANE Select: NM_001347995
dbSNP: rs145135759
Type: single nucleotide variant
Location: chr9:69391755 (GRCh38)
Structure: AlphaFold pLDDT 60.47

Full ENTREP1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

ENTREP1 p.Ala374Ser Uncertain significance ★ ⚠ same type
ENTREP1 p.Ala418Asp Uncertain significance ★ ⚠ same type
ENTREP1 p.Ala440Ser Uncertain significance ★ ⚠ same type
ENTREP1 p.Ala440Thr Uncertain significance ★ ⚠ same type
ENTREP1 p.Ala448Ser Uncertain significance ★ ⚠ same type
ENTREP1 p.Ala492Val Uncertain significance ★ ⚠ same type
ENTREP1 p.Ala574Pro Uncertain significance ★ ⚠ same type
ENTREP1 p.Arg191Gly 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/entrep1-p-ala588val (accessed [today's date]).

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