Is BMPR1A p.Pro136fs (c.405dup) pathogenic?

BMPR1A p.Pro136fs (c.405dup) is classified Pathogenic in BMPR1A (ClinVar, Multiple submitters, 6 submitters; last evaluated 2024-08-07). No gnomAD frequency available for this variant; Associated with juvenile polyposis syndrome.

What condition is associated with BMPR1A p.Pro136fs (c.405dup)?

BMPR1A p.Pro136fs (c.405dup) is associated with juvenile polyposis syndrome, hereditary neoplastic syndrome (ClinVar).

How common is BMPR1A p.Pro136fs (c.405dup) in the general population?

BMPR1A p.Pro136fs (c.405dup) is no gnomAD frequency available for this variant (gnomAD).

How is Juvenile polyposis syndrome inherited?

Typically Autosomal dominant (Orphanet). A genetic counselor can assess individual risk for a family.

BMPR1A p.Pro136fs

c.405dup · rs876660442 · VCV233491

Pathogenic Multiple submitters

Classification

Pathogenic

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 6 submitters

Consequence

frameshift

predicted LoF

gnomAD v4.1

Not reported

no gnomAD frequency available for this variant

Conditions

juvenile polyposis syndrome

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequence	frameshift	predicted loss-of-function in a haploinsufficient gene (ClinGen)
NMD	predicted	premature termination codon in exon 6 of 13
Splicing
SpliceAI	—	not assessed · substitutions only
Constraint at this position
Conservation	phyloP 7.6	GERP 2.6, 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: BMPR1A
Protein: p.Pro136fs
Coding: c.405dup
MANE Select: NM_004329
dbSNP: rs876660442
Type: Duplication
Location: chr10:86899863 (GRCh38)
Gene constraint: LOEUF 0.195 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 82.86 · 11 PDB

Full BMPR1A gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

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

Also linked: hereditary neoplastic syndrome

For Juvenile polyposis syndrome (Orphanet):

Inheritance: Autosomal dominant
Onset: Adolescent, Adult, Childhood, Infancy
Prevalence: 1-9 / 100 000 (Europe)

Similar variants

BMPR1A p.Pro136Leu Uncertain significance ★★ ⚠ same residue
BMPR1A p.Pro136= Likely benign ★ same residue
BMPR1A p.Arg442fs Pathogenic ★★ same condition
BMPR1A p.Asn73Ter Pathogenic ★★ same condition
BMPR1A p.Asp38fs Pathogenic ★★ same condition
BMPR1A p.Ile308fs Pathogenic ★★ same condition
BMPR1A p.Leu193fs Pathogenic ★★ same condition
BMPR1A p.Leu59fs 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/bmpr1a-p-pro136fs (accessed [today's date]).

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