Is BRCA1 p.Pro798= (c.2394A>G) pathogenic?

BRCA1 p.Pro798= (c.2394A>G) is classified Likely benign in BRCA1 (ClinVar, Single submitter, 1 submitter; last evaluated 2024-02-13). Absent from gnomAD v4.1; Associated with hereditary breast ovarian cancer syndrome.

What condition is associated with BRCA1 p.Pro798= (c.2394A>G)?

BRCA1 p.Pro798= (c.2394A>G) is associated with hereditary breast ovarian cancer syndrome (ClinVar).

How common is BRCA1 p.Pro798= (c.2394A>G) in the general population?

BRCA1 p.Pro798= (c.2394A>G) is absent from gnomAD v4.1 (gnomAD).

How is Hereditary breast and/or ovarian cancer syndrome inherited?

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

BRCA1 p.Pro798=

c.2394A>G · rs2552189204 · VCV2131373

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

hereditary breast ovarian cancer 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 0.72	GERP -0.8, phastCons 0.29
Overall
CADD	1.316	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: BRCA1
Protein: p.Pro798=
Coding: c.2394A>G
MANE Select: NM_007294
dbSNP: rs2552189204
Type: single nucleotide variant
Location: chr17:43093137 (GRCh38)
Gene constraint: LOEUF 0.885 · pLI <0.01 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 41.99 · 33 PDB
Residue 798: a UniProt-annotated variant site (in bc; uncertain significance; functionally neutral in vitro)

Full BRCA1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

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

For Hereditary breast and/or ovarian cancer syndrome (Orphanet):

Inheritance: Autosomal dominant
Onset: Adult, Elderly

Similar variants

BRCA1 p.Pro798Arg Conflicting classifications of pathogenicity ★ ⚠ same residue
BRCA1 p.Pro798Leu Conflicting classifications of pathogenicity ★ ⚠ same residue
BRCA1 p.Pro798Ser Conflicting classifications of pathogenicity ★ ⚠ same residue
BRCA1 p.Pro798Gln Uncertain significance ★ ⚠ same residue
BRCA1 p.Pro798Thr Conflicting classifications of pathogenicity ★ ⚠ same residue
BRCA1 p.Pro798Ala Likely benign ★ same residue
BRCA1 c.134+3A>T Likely pathogenic ★★★ same condition
BRCA1 c.135-1G>T 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/brca1-p-pro798 (accessed [today's date]).

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