Is NBEA p.Pro609Ser (c.1825C>T) pathogenic?

NBEA p.Pro609Ser (c.1825C>T) is classified Uncertain significance in NBEA (ClinVar, Single submitter, 1 submitter; last evaluated 2026-05-11). AlphaMissense: ambiguous (0.4981); Very rare (popmax 0.00034%, nfe); Associated with Inborn genetic diseases.

What condition is associated with NBEA p.Pro609Ser (c.1825C>T)?

NBEA p.Pro609Ser (c.1825C>T) is associated with Inborn genetic diseases (ClinVar).

How common is NBEA p.Pro609Ser (c.1825C>T) in the general population?

NBEA p.Pro609Ser (c.1825C>T) is very rare (popmax 0.00034%, nfe) (gnomAD).

What do computational predictors say about NBEA p.Pro609Ser (c.1825C>T)?

AlphaMissense predicts ambiguous (score 0.4981) — an in-silico prediction, not a clinical call.

NBEA p.Pro609Ser

c.1825C>T · VCV4860743

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

ambiguous

0.4981 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00034%, nfe)

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.4981	ambiguous
REVEL	0.308	indeterminate
SaProt	—	not scored · why
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 7.6	GERP 1.9, phastCons 1
Regional constraint	o/e 0.69	unconstrained · MANE · 86 kb · p 2.9e-12 · regional, not allelic
Overall
CADD	26.2	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL is an independent agreement signal.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00034% European (non-Finnish) · 4/1,176,426 alleles

Filtering AF 8e-05% ClinGen BA1/BS1 input FAF95, joint · FAF99 5.4e-05%

Overall 0.000249% 4/1,603,650 alleles · very rare exomes 2/1,451,550 · genomes 2/152,100 · joint denominator

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: NBEA
Protein: p.Pro609Ser
Coding: c.1825C>T
MANE Select: NM_001385012
Type: single nucleotide variant
Location: chr13:35109434 (GRCh38)
Gene constraint: LOEUF 0.137 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Residue 609: a UniProt-annotated variant site (in nedege)

Full NBEA 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

NBEA p.Arg1299Ter Pathogenic/Likely pathogenic ★★ same condition
NBEA p.Arg1325Gln Uncertain significance ★★ same condition
NBEA p.Arg2277Gln Uncertain significance ★★ same condition
NBEA p.Arg2291Gly Uncertain significance ★★ ⚠ same condition
NBEA p.Asp701Glu Uncertain significance ★★ ⚠ same condition
NBEA p.Gln2141Arg Uncertain significance ★★ ⚠ same condition
NBEA p.Glu971Asp Uncertain significance ★★ ⚠ same condition
NBEA p.Gly39Asp 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/nbea-p-pro609ser (accessed [today's date]).

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