Is ESPL1 p.Pro1813= (c.5439C>T) pathogenic?

ESPL1 p.Pro1813= (c.5439C>T) is classified Likely benign in ESPL1 (ClinVar, No assertion criteria, 1 submitter; last evaluated 2019-11-25). Rare (popmax 0.327%, afr); Associated with ESPL1-related disorder.

What condition is associated with ESPL1 p.Pro1813= (c.5439C>T)?

ESPL1 p.Pro1813= (c.5439C>T) is associated with ESPL1-related disorder (ClinVar).

How common is ESPL1 p.Pro1813= (c.5439C>T) in the general population?

ESPL1 p.Pro1813= (c.5439C>T) is rare (popmax 0.327%, afr) (gnomAD).

ESPL1 p.Pro1813=

c.5439C>T · rs143830681 · VCV3033197

Likely benign No assertion criteria

Classification

Likely benign

ClinVar

Review

No assertion criteria ☆☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

rare (popmax 0.327%, afr)

Conditions

ESPL1-related disorder

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP -9.7	GERP -3.5
Overall
CADD	0.575	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.327% African / African-American · 245/74,970 alleles

Filtering AF 0.293% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.28%

Overall 0.0169% 271/1,606,780 alleles · rare

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.327%	306
Remaining individualsnot grpmax-eligible	0.0177%	5,649
Admixed American	0.0153%	6,537
South Asian	0.00111%	89,706
European (non-Finnish)	0.000425%	235,405

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: ESPL1
Protein: p.Pro1813=
Coding: c.5439C>T
MANE Select: NM_012291
dbSNP: rs143830681
Type: single nucleotide variant
Location: chr12:53290915 (GRCh38)
Gene constraint: LOEUF 0.292 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 75.67 · 9 PDB

Full ESPL1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

ESPL1-related disorder

Similar variants

ESPL1 p.Ser1239Ter Uncertain significance ★ same condition
ESPL1 c.6161+7C>T Likely benign same condition
ESPL1 p.Ala116Val Benign ⚠ same condition
ESPL1 p.Ala1438= Likely benign same condition
ESPL1 p.Arg1318Gln Likely benign same condition
ESPL1 p.Asn1723= Likely benign same condition
ESPL1 p.Asp1351= Likely benign same condition
ESPL1 p.Gly1510Arg Likely benign 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/espl1-p-pro1813 (accessed [today's date]).

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