Is GDAP1 p.Thr147fs (c.439del) pathogenic?

GDAP1 p.Thr147fs (c.439del) is classified Uncertain significance in GDAP1 (ClinVar, No assertion criteria, 2 submitters; last evaluated 2016-01-06). No gnomAD frequency available for this variant; Associated with Charcot-Marie-Tooth disease.

What condition is associated with GDAP1 p.Thr147fs (c.439del)?

GDAP1 p.Thr147fs (c.439del) is associated with Charcot-Marie-Tooth disease, Charcot-Marie-Tooth disease recessive intermediate A (ClinVar).

How common is GDAP1 p.Thr147fs (c.439del) in the general population?

GDAP1 p.Thr147fs (c.439del) is no gnomAD frequency available for this variant (gnomAD).

GDAP1 p.Thr147fs

c.439del · rs1586803279 · VCV637109

Uncertain significance No assertion criteria

Classification

Uncertain significance

ClinVar

Review

No assertion criteria ☆☆☆☆

ClinVar · 2 submitters

Consequence

frameshift

predicted LoF

gnomAD v4.1

Not reported

no gnomAD frequency available for this variant

Conditions

Charcot-Marie-Tooth disease

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequence	frameshift	predicted loss-of-function
NMD	predicted	premature termination codon in exon 3 of 6
Splicing
SpliceAI	—	not assessed · substitutions only
Constraint at this position
Conservation	phyloP 7.9	GERP 2.1, phastCons 1

Predicted loss-of-function is descriptive, not an applied PVS1 code.

Population frequency

dbSNP / gnomAD

No gnomAD frequency available for this variant. This is missing data, not an absence: the variant may or may not be present in gnomAD. Rarity (ACMG PM2) and BA1/BS1 cannot be assessed for it.

Variant & gene context

Gene: GDAP1
Protein: p.Thr147fs
Coding: c.439del
MANE Select: NM_018972
dbSNP: rs1586803279
Type: Deletion
Location: chr8:74360264 (GRCh38)
Gene constraint: LOEUF 0.963 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 87.68 · 8 PDB

Full GDAP1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Charcot-Marie-Tooth disease — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: Charcot-Marie-Tooth disease recessive intermediate A

Similar variants

GDAP1 p.Glu168fs Pathogenic/Likely pathogenic ★★ same condition
GDAP1 p.Met1fs Pathogenic/Likely pathogenic ★★ same condition
GDAP1 p.Phe263fs Pathogenic/Likely pathogenic ★★ same condition
GDAP1 p.Tyr279_Tyr280insTer Pathogenic/Likely pathogenic ★★ same condition
GDAP1 p.Asp134fs Pathogenic ★ same condition
GDAP1 p.Glu145fs Pathogenic ★ same condition
GDAP1 p.Ile186fs Pathogenic ★ same condition
GDAP1 p.Lys193fs 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/gdap1-p-thr147fs (accessed [today's date]).

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