Is PTPRF p.Val1137= (c.3411G>A) pathogenic?

PTPRF p.Val1137= (c.3411G>A) is classified Benign in PTPRF (ClinVar, Single submitter, 1 submitter; last evaluated 2024-11-26). Common (popmax 77.9%, nfe) — too common for a highly-penetrant pathogenic allele.

PTPRF p.Val1137=

Q: How common is PTPRF p.Val1137= (c.3411G>A) in the general population?

PTPRF p.Val1137= (c.3411G>A) is common (popmax 77.9%, nfe) — too common for a highly-penetrant pathogenic allele (gnomAD).

c.3411G>A · VCV4971712

Benign Single submitter

Classification

Benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Common

common (popmax 77.9%, nfe) — too common for a highly-penetrant pathogenic allele

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
REVEL	0.218	benign-leaning
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 0.41	GERP -2.8, phastCons 0.98
Overall
CADD	1.805	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 77.9% European (non-Finnish) · 919,012/1,179,868 alleles

Filtering AF 77.8% ClinGen BA1/BS1 input FAF95, joint · FAF99 77.7%

Overall 74.1% 1,196,013/1,613,788 alleles · common

Ancestry group	Frequency	1 in
Finnishnot grpmax-eligible	79.4%	1
European (non-Finnish)grpmax	77.9%	1
Amishnot grpmax-eligible	77.6%	1
East Asian	74.9%	1
Remaining individualsnot grpmax-eligible	72.7%	1
Ashkenazi Jewishnot grpmax-eligible	71.4%	1
Middle Eastern	68.5%	1
South Asian	59.6%	2
Admixed American	53.6%	2
African / African-American	46.3%	2

Finnish shows a higher raw frequency than the grpmax group above it. gnomAD excludes bottlenecked groups — Finnish, Ashkenazi Jewish, Amish and “Remaining individuals” — from grpmax, because founder effects make their frequencies unrepresentative for filtering. The table is sorted by frequency, so an excluded group can sit above the grpmax row.

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: PTPRF
Protein: p.Val1137=
Coding: c.3411G>A
MANE Select: NM_002840
Type: single nucleotide variant
Location: chr1:43605550 (GRCh38)
Gene constraint: LOEUF 0.348 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 82.43 · 13 PDB

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

Similar variants

PTPRF p.Gly1143Ser Uncertain significance ★★ ⚠ same type
PTPRF p.His1730Gln Uncertain significance ★★ ⚠ same type
PTPRF c.1531+9G>A Benign/Likely benign ★★ same type
PTPRF c.1668+10G>C Benign/Likely benign ★★ same type
PTPRF c.237+5G>A Benign ★★ same type
PTPRF c.3974-9C>T Benign ★★ same type
PTPRF p.Ala1659= Benign ★★ same type
PTPRF p.Ala356Ser Likely 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/ptprf-p-val1137 (accessed [today's date]).

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