Is BRCA2 p.Ser2373Arg (c.7119C>A) pathogenic?

BRCA2 p.Ser2373Arg (c.7119C>A) is classified Uncertain significance in BRCA2 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2026-03-04). AlphaMissense: likely benign (0.257); Absent from gnomAD v4.1; Associated with hereditary neoplastic syndrome.

What condition is associated with BRCA2 p.Ser2373Arg (c.7119C>A)?

BRCA2 p.Ser2373Arg (c.7119C>A) is associated with hereditary neoplastic syndrome, hereditary breast ovarian cancer syndrome (ClinVar).

How common is BRCA2 p.Ser2373Arg (c.7119C>A) in the general population?

BRCA2 p.Ser2373Arg (c.7119C>A) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about BRCA2 p.Ser2373Arg (c.7119C>A)?

AlphaMissense predicts likely benign (score 0.257) — an in-silico prediction, not a clinical call.

BRCA2 p.Ser2373Arg

c.7119C>A · rs786202624 · VCV1943891

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

AlphaMissense

likely benign

0.257 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
AlphaMissense	0.257	likely benign
REVEL	0.43	indeterminate
SaProt	—	not scored · why
Splicing
SpliceAI	<0.2	no splice effect predicted · four deltas, not one · how we know
Constraint at this position
Conservation	phyloP 2.2	GERP 1.6, phastCons 0.98
Regional constraint	o/e 1.03	unconstrained · MANE · 47 kb · p 0.059 · regional, not allelic
Overall
CADD	20.1	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL is an independent agreement signal.

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: BRCA2
Protein: p.Ser2373Arg
Coding: c.7119C>A
MANE Select: NM_000059
dbSNP: rs786202624
Type: single nucleotide variant
Location: chr13:32354972 (GRCh38)
Gene constraint: LOEUF 0.803 · pLI <0.01 · ClinGen HI 3/3 (gnomAD)
Residue 2373: the 'interaction with fancd2' region

Full BRCA2 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: hereditary breast ovarian cancer syndrome

Similar variants

BRCA2 p.Ser2373Gly Uncertain significance ★★ same residue
BRCA2 p.Ser2373Asn Uncertain significance ★ same residue
BRCA2 p.Ser2373= Likely benign ★ same residue
BRCA2 p.Ser2373fs Pathogenic ★ same residue
BRCA2 p.Ser2373Thr Uncertain significance same residue
BRCA2 c.316+1G>T Pathogenic ★★★ same condition
BRCA2 c.316+2T>C Pathogenic ★★★ same condition
BRCA2 c.316+5G>A 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/brca2-p-ser2373arg (accessed [today's date]).

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