Is IFT122 p.Asp342Val (c.1025A>T) pathogenic?

IFT122 p.Asp342Val (c.1025A>T) is classified Likely pathogenic in IFT122 (ClinVar, Single submitter, 1 submitter; last evaluated 2022-01-01). AlphaMissense: likely pathogenic (0.9629); Ultra-rare (popmax 0.0579%, eas); Associated with cranioectodermal dysplasia 1.

What condition is associated with IFT122 p.Asp342Val (c.1025A>T)?

IFT122 p.Asp342Val (c.1025A>T) is associated with cranioectodermal dysplasia 1 (ClinVar).

How common is IFT122 p.Asp342Val (c.1025A>T) in the general population?

IFT122 p.Asp342Val (c.1025A>T) is ultra-rare (popmax 0.0579%, eas) (gnomAD).

What do computational predictors say about IFT122 p.Asp342Val (c.1025A>T)?

AlphaMissense predicts likely pathogenic (score 0.9629) — an in-silico prediction, not a clinical call.

IFT122 p.Asp342Val

c.1025A>T · VCV2431224

Likely pathogenic Single submitter

Classification

Likely pathogenic

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.9629 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.0579%, eas)

Missense predictors

3/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

cranioectodermal dysplasia 1

Computational evidence

Protein change
AlphaMissense	0.9629	likely pathogenic ✓ concordant with ClinVar
REVEL	0.94	strongly pathogenic-leaning
SaProt	LLR -16.76	damaging
⇒ AlphaMissense, REVEL and SaProt all call this damaging.
Splicing
SpliceAI	<0.2	no splice effect predicted · four deltas, not one · how we know
Constraint at this position
Conservation	phyloP 11	GERP 2.2, phastCons 1
Regional constraint	o/e 0.84	unconstrained · MANE · 25 kb · p 4.4e-05 · regional, not allelic
Overall
CADD	26.1	PHRED · no single calibrated threshold — expert panels disagree

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

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0579% East Asian · 26/44,882 alleles

Filtering AF 0.0405% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0347%

Overall 0.00161% 26/1,614,062 alleles · ultra-rare exomes 23/1,461,890 · genomes 3/152,172 · 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: IFT122
Protein: p.Asp342Val
Coding: c.1025A>T
MANE Select: NM_052989
Type: single nucleotide variant
Location: chr3:129476679 (GRCh38)
Gene constraint: LOEUF 0.811 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 82.91 · 5 PDB

Full IFT122 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

cranioectodermal dysplasia 1 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

IFT122 p.Asp342Asn Uncertain significance ★★ ⚠ same residue
IFT122 p.Asp342= Conflicting classifications of pathogenicity ★ same residue
IFT122 c.1148-1G>C Pathogenic/Likely pathogenic ★★ same condition
IFT122 c.272+1G>A Likely pathogenic ★★ same condition
IFT122 c.273-257C>A Pathogenic/Likely pathogenic ★★ same condition
IFT122 c.3265+1G>A Pathogenic/Likely pathogenic ★★ same condition
IFT122 p.Arg1185Ter Pathogenic/Likely pathogenic ★★ same condition
IFT122 p.Arg189Ter Pathogenic/Likely pathogenic ★★ 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/ift122-p-asp342val (accessed [today's date]).

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