Is CELSR2 p.Ser507Thr (c.1520G>C) pathogenic?

CELSR2 p.Ser507Thr (c.1520G>C) is classified Uncertain significance in CELSR2 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2023-05-01). AlphaMissense: ambiguous (0.4005); Ultra-rare (popmax 0.0164%, mid).

How common is CELSR2 p.Ser507Thr (c.1520G>C) in the general population?

CELSR2 p.Ser507Thr (c.1520G>C) is ultra-rare (popmax 0.0164%, mid) (gnomAD).

What do computational predictors say about CELSR2 p.Ser507Thr (c.1520G>C)?

AlphaMissense predicts ambiguous (score 0.4005) — an in-silico prediction, not a clinical call.

CELSR2 p.Ser507Thr

c.1520G>C · rs144587788 · VCV2457429

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

AlphaMissense

ambiguous

0.4005 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.0164%, mid)

Computational evidence

Protein change
AlphaMissense	0.4005	ambiguous
REVEL	0.24	benign-leaning
SaProt	—	not scored · why
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 12	GERP 2, phastCons 1
Regional constraint	o/e 0.90	unconstrained · MANE · 1,783 bp · p 0.0042 · regional, not allelic
Overall
CADD	25.0	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 0.0164% Middle Eastern · 1/6,084 alleles

Filtering AF 0.00543% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0038%

Overall 0.00675% 109/1,613,718 alleles · ultra-rare exomes 70/1,461,572 · genomes 39/152,146 · joint denominator

Ancestry group	Frequency	1 in
Amishnot grpmax-eligible	3.3%	30
Ashkenazi Jewishnot grpmax-eligible	0.0912%	1,097
Middle Easterngrpmax	0.0164%	6,084
Admixed American	0.0117%	8,573
Remaining individualsnot grpmax-eligible	0.0096%	10,413
European (non-Finnish)	0.00322%	31,051

Amish shows a higher raw frequency than the grpmax group above it. gnomAD excludes bottlenecked groups — Finnish, Ashkenazi Jewish, Amish and “Remaining individuals” — from grpmax, because founder effects make their frequencies unrepresentative for filtering. The table is sorted by frequency, so an excluded group can sit above the grpmax row.

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: CELSR2
Protein: p.Ser507Thr
Coding: c.1520G>C
MANE Select: NM_001408
dbSNP: rs144587788
Type: single nucleotide variant
Location: chr1:109251599 (GRCh38)
Gene constraint: LOEUF 0.396 · pLI 1.00 (gnomAD)
Residue 507: the cadherin 4 domain

Full CELSR2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

CELSR2 c.8338+1G>C Uncertain significance ★★ same type
CELSR2 p.Ala1114Val Uncertain significance ★★ ⚠ same type
CELSR2 p.Ala2145Thr Uncertain significance ★★ ⚠ same type
CELSR2 p.Ala2574Thr Uncertain significance ★★ ⚠ same type
CELSR2 p.Arg1171Gln Uncertain significance ★★ ⚠ same type
CELSR2 p.Arg1328His Uncertain significance ★★ ⚠ same type
CELSR2 p.Arg1400His Uncertain significance ★★ same type
CELSR2 p.Arg1978Gln 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/celsr2-p-ser507thr (accessed [today's date]).

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