Is CDH23 p.Asp2953= (c.8859C>T) pathogenic?

CDH23 p.Asp2953= (c.8859C>T) is classified Conflicting classifications of pathogenicity in CDH23 (ClinVar, Conflicting submitters, 7 submitters; last evaluated 2026-02-04). Rare (popmax 0.98%, eas); Associated with autosomal recessive nonsyndromic hearing loss 12.

What condition is associated with CDH23 p.Asp2953= (c.8859C>T)?

CDH23 p.Asp2953= (c.8859C>T) is associated with autosomal recessive nonsyndromic hearing loss 12, Usher syndrome type 1, Usher syndrome type 1D (ClinVar).

How common is CDH23 p.Asp2953= (c.8859C>T) in the general population?

CDH23 p.Asp2953= (c.8859C>T) is rare (popmax 0.98%, eas) (gnomAD).

CDH23 p.Asp2953=

c.8859C>T · rs11000008 · VCV46057

Conflicting classifications of pathogenicity Conflicting submitters

Classification

Conflicting classifications of pathogenicity

ClinVar

Review

Conflicting submitters ★☆☆☆

ClinVar · 7 submitters

gnomAD v4.1

Rare

rare (popmax 0.98%, eas)

Conditions

autosomal recessive nonsyndromic hearing loss 12

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 -12	GERP -3.4
Overall
CADD	0.153	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.98% East Asian · 440/44,882 alleles

Filtering AF 0.905% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.875%

Overall 0.0312% 503/1,612,330 alleles · rare

Ancestry group	Frequency	1 in
East Asiangrpmax	0.98%	102
Remaining individualsnot grpmax-eligible	0.0432%	2,314
Ashkenazi Jewishnot grpmax-eligible	0.0304%	3,290
South Asian	0.0143%	7,006
African / African-American	0.00266%	37,524
Admixed American	0.00167%	60,028
European (non-Finnish)	0.000932%	107,262

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: CDH23
Protein: p.Asp2953=
Coding: c.8859C>T
MANE Select: NM_022124
dbSNP: rs11000008
Type: single nucleotide variant
Location: chr10:71809956 (GRCh38)
Gene constraint: LOEUF 0.685 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Residue 2953: the cadherin 27 domain

Full CDH23 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

autosomal recessive nonsyndromic hearing loss 12 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: Usher syndrome type 1 Usher syndrome type 1D

Similar variants

CDH23 p.Asp2953Asn Uncertain significance ★ same residue
CDH23 p.Arg2029Trp Pathogenic ★★★ ⚠ same condition
CDH23 p.Asp127Gly Likely pathogenic ★★★ same condition
CDH23 p.Glu956Lys Pathogenic ★★★ same condition
CDH23 p.Pro240Leu Pathogenic ★★★ same condition
CDH23 c.1515-12G>A Uncertain significance ★★★ same condition
CDH23 p.Ala3190Val Uncertain significance ★★★ ⚠ same condition
CDH23 p.Arg301Gln 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/cdh23-p-asp2953 (accessed [today's date]).

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