Is MEN1 p.Arg295fs (c.881dup) pathogenic?

MEN1 p.Arg295fs (c.881dup) is classified Pathogenic in MEN1 (ClinVar, Single submitter, 1 submitter; last evaluated 2023-08-07). Absent from gnomAD; Associated with multiple endocrine neoplasia type 1.

What condition is associated with MEN1 p.Arg295fs (c.881dup)?

MEN1 p.Arg295fs (c.881dup) is associated with multiple endocrine neoplasia type 1 (ClinVar).

How common is MEN1 p.Arg295fs (c.881dup) in the general population?

MEN1 p.Arg295fs (c.881dup) is absent from gnomAD (gnomAD).

How is Multiple endocrine neoplasia type 1 inherited?

Typically Autosomal dominant, Not applicable (Orphanet). A genetic counselor can assess individual risk for a family.

MEN1 p.Arg295fs

c.881dup · rs2497187010 · VCV2750762

Pathogenic Single submitter

Classification

Pathogenic

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

Consequence

frameshift

predicted LoF

gnomAD v4.1

Not reported

no gnomAD frequency available for this variant

Conditions

multiple endocrine neoplasia type 1

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 10
Splicing
SpliceAI	—	not assessed · substitutions only
Constraint at this position
Conservation	phyloP 3.8	GERP -1.5, 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: MEN1
Protein: p.Arg295fs
Coding: c.881dup
MANE Select: NM_001370259
dbSNP: rs2497187010
Type: Duplication
Location: chr11:64807041 (GRCh38)
Gene constraint: LOEUF 0.206 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 85.13 · 69 PDB
Residue 295: the 'interaction with fancd2' region; an α-helix

Full MEN1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

multiple endocrine neoplasia type 1 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Multiple endocrine neoplasia type 1 (Orphanet):

Inheritance: Autosomal dominant, Not applicable
Onset: All ages
Prevalence: 1-9 / 100 000 (Europe)

Similar variants

MEN1 p.Arg295= Likely benign ★★ same residue
MEN1 p.Arg295Gln Conflicting classifications of pathogenicity ★ same residue
MEN1 p.Arg295Trp Conflicting classifications of pathogenicity ★ ⚠ same residue
MEN1 p.Ala380fs Pathogenic ★★ same condition
MEN1 p.Ala467fs Pathogenic ★★ same condition
MEN1 p.Arg108fs Pathogenic ★★ same condition
MEN1 p.Asp123fs Pathogenic ★★ same condition
MEN1 p.Asp136fs 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/men1-p-arg295fs (accessed [today's date]).

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