Is PTEN p.Phe347= (c.1041C>T) pathogenic?

PTEN p.Phe347= (c.1041C>T) is classified Benign/Likely benign in PTEN (ClinVar, Multiple submitters, 4 submitters; last evaluated 2025-02-13). Very rare (popmax 8.5e-05%, nfe); Associated with hereditary neoplastic syndrome.

What condition is associated with PTEN p.Phe347= (c.1041C>T)?

PTEN p.Phe347= (c.1041C>T) is associated with hereditary neoplastic syndrome, Cowden syndrome 1, macrocephaly-autism syndrome (ClinVar).

How common is PTEN p.Phe347= (c.1041C>T) in the general population?

PTEN p.Phe347= (c.1041C>T) is very rare (popmax 8.5e-05%, nfe) (gnomAD).

PTEN p.Phe347=

c.1041C>T · rs1554826029 · VCV536565

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 4 submitters

gnomAD v4.1

Rare

very rare (popmax 8.5e-05%, nfe)

Conditions

hereditary neoplastic syndrome

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 1.1	GERP -0.48, phastCons 1
Overall
CADD	7.839	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 8.5e-05% European (non-Finnish) · 1/1,177,156 alleles

Overall 6.86e-05% 1/1,457,192 alleles · very rare

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: PTEN
Protein: p.Phe347=
Coding: c.1041C>T
MANE Select: NM_000314
dbSNP: rs1554826029
Type: single nucleotide variant
Location: chr10:87965301 (GRCh38)
Gene constraint: LOEUF 0.685 · pLI 0.05 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 83.76 · 12 PDB
Residue 347: a UniProt-annotated variant site (in cws1; reduced phosphatase activity towards ins(1,3,4,5)p4); a β-strand; the c2 tensin-type domain; the 'required for interaction with nop53' region; a UniProt-annotated variant site (in mcephas)

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

Disease context

hereditary neoplastic syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: Cowden syndrome 1 macrocephaly-autism syndrome familial meningioma glioma susceptibility 2 PTEN hamartoma tumor syndrome prostate cancer, hereditary

Similar variants

PTEN p.Phe347Leu Uncertain significance ★ ⚠ same residue
PTEN p.Phe347Ser Uncertain significance ★ ⚠ same residue
PTEN p.Phe347fs Likely pathogenic ★ same residue
PTEN p.Phe347del Uncertain significance ★ same residue
PTEN c.1026+1G>A Pathogenic ★★★ same condition
PTEN c.1027-1852A>G Likely pathogenic ★★★ same condition
PTEN c.1027-1G>A Pathogenic ★★★ same condition
PTEN c.165-1G>A 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/pten-p-phe347 (accessed [today's date]).

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