Is BRCA2 p.Ala2633Val (c.7898C>T) pathogenic?

BRCA2 p.Ala2633Val (c.7898C>T) is classified Likely benign in BRCA2 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-05-19). AlphaMissense: ambiguous (0.524); Absent from gnomAD v4.1; Associated with hereditary neoplastic syndrome.

What condition is associated with BRCA2 p.Ala2633Val (c.7898C>T)?

BRCA2 p.Ala2633Val (c.7898C>T) is associated with hereditary neoplastic syndrome (ClinVar).

How common is BRCA2 p.Ala2633Val (c.7898C>T) in the general population?

BRCA2 p.Ala2633Val (c.7898C>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about BRCA2 p.Ala2633Val (c.7898C>T)?

AlphaMissense predicts ambiguous (score 0.524) — an in-silico prediction, not a clinical call.

BRCA2 p.Ala2633Val

c.7898C>T · rs1555286846 · VCV1761065

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

ambiguous

0.524 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
AlphaMissense	0.524	ambiguous · top 8% in BRCA2
REVEL	0.652	pathogenic-leaning
SaProt	—	not scored · why
Splicing
SpliceAI	<0.2	all four deltas below 0.2 · C>G here scores Δ0.84 · evaluated, not missing
Constraint at this position
Conservation	phyloP 7.6	GERP 2.5, phastCons 1
Regional constraint	o/e 1.03	unconstrained · MANE · 47 kb · p 0.059 · regional, not allelic
Overall
CADD	26.6	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.Ala2633Val
Coding: c.7898C>T
MANE Select: NM_000059
dbSNP: rs1555286846
Type: single nucleotide variant
Location: chr13:32362615 (GRCh38)
Gene constraint: LOEUF 0.803 · pLI <0.01 · ClinGen HI 3/3 (gnomAD)
Residue 2633: the 'interaction with sem1' 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

Similar variants

BRCA2 p.Ala2633= Likely benign ★★ same residue
BRCA2 p.Ala2633Gly Uncertain significance ★ same residue
BRCA2 p.Ala2633Ser Conflicting classifications of pathogenicity ★ same residue
BRCA2 p.Ala2633fs Pathogenic ★★ same residue
BRCA2 p.Ala2633Thr 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-ala2633val (accessed [today's date]).

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