Is CCN1 p.Ala36Val (c.107C>T) pathogenic?

CCN1 p.Ala36Val (c.107C>T) is classified Uncertain significance in CCN1 (ClinVar, Single submitter, 1 submitter; last evaluated 2023-08-15). AlphaMissense: likely benign (0.0567); Rare (popmax 0.399%, eas).

How common is CCN1 p.Ala36Val (c.107C>T) in the general population?

CCN1 p.Ala36Val (c.107C>T) is rare (popmax 0.399%, eas) (gnomAD).

What do computational predictors say about CCN1 p.Ala36Val (c.107C>T)?

AlphaMissense predicts likely benign (score 0.0567) — an in-silico prediction, not a clinical call.

CCN1 p.Ala36Val

c.107C>T · rs145852662 · VCV2618958

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.0567 · ACMG-weighted

gnomAD v4.1

Rare

rare (popmax 0.399%, eas)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.0567	likely benign
REVEL	0.079	moderately benign-leaning
SaProt	LLR -6.82	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 3.9	GERP 0.062, phastCons 1
Overall
CADD	19.17	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification

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

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.399% East Asian · 176/44,078 alleles

Filtering AF 0.351% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.333%

Overall 0.0112% 180/1,600,804 alleles · rare

Ancestry group	Frequency	1 in
East Asiangrpmax	0.399%	250
Remaining individualsnot grpmax-eligible	0.00485%	20,615
European (non-Finnish)	8.51e-05%	1,175,062

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: CCN1
Protein: p.Ala36Val
Coding: c.107C>T
MANE Select: NM_001237 · reported on NM_001554
dbSNP: rs145852662
Type: single nucleotide variant
Location: chr1:85581408 (GRCh38)
Structure: AlphaFold pLDDT 73.80 · 115 PDB
Residue 36: the 'disordered' region

Full CCN1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

EXOSC9 p.Ala438Val Uncertain significance ★★ ⚠ same type
CCN1 c.277+50G>C Benign ★★ same type
CCN1 c.64-124G>A Benign ★★ same type
CCN1 c.-107C>A Benign ★★ same type
CCN1 p.Ser316Cys Likely benign ★★ ⚠ same type
CCN1 p.Tyr300= Benign ★★ same type
CCNA2 c.*828C>G Benign ★★ same type
CCNA2 p.Leu126= Benign ★★ 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/ccn1-p-ala36val (accessed [today's date]).

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