Is BRCA2 p.Asp191Ala (c.572A>C) pathogenic?

BRCA2 p.Asp191Ala (c.572A>C) is classified Uncertain significance in BRCA2 (ClinVar, Single submitter, 1 submitter; last evaluated 2020-06-29). AlphaMissense: ambiguous (0.4142); Absent from gnomAD v4.1; Associated with hereditary neoplastic syndrome.

What condition is associated with BRCA2 p.Asp191Ala (c.572A>C)?

BRCA2 p.Asp191Ala (c.572A>C) is associated with hereditary neoplastic syndrome (ClinVar).

How common is BRCA2 p.Asp191Ala (c.572A>C) in the general population?

BRCA2 p.Asp191Ala (c.572A>C) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about BRCA2 p.Asp191Ala (c.572A>C)?

AlphaMissense predicts ambiguous (score 0.4142) — an in-silico prediction, not a clinical call.

BRCA2 p.Asp191Ala

c.572A>C · rs397507798 · VCV1171461

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

ambiguous

0.4142 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

hereditary neoplastic syndrome

Computational evidence

Protein change
AlphaMissense	0.4142	ambiguous · top 10% in BRCA2
REVEL	0.244	benign-leaning
SaProt	—	not scored · why
Splicing
SpliceAI	<0.2	all four deltas below 0.2 · A>G here scores Δ0.87 · evaluated, not missing
Constraint at this position
Conservation	phyloP 11	GERP 2.3, phastCons 1
Regional constraint	o/e 1.03	unconstrained · MANE · 47 kb · p 0.059 · regional, not allelic
Overall
CADD	23.7	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.Asp191Ala
Coding: c.572A>C
MANE Select: NM_000059
dbSNP: rs397507798
Type: single nucleotide variant
Location: chr13:32326554 (GRCh38)
Gene constraint: LOEUF 0.803 · pLI <0.01 · ClinGen HI 3/3 (gnomAD)

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.Asp191Asn Uncertain significance ★★ ⚠ same residue
BRCA2 p.Asp191Gly Conflicting classifications of pathogenicity ★ same residue
BRCA2 p.Asp191Val Conflicting classifications of pathogenicity ★ same residue
BRCA2 p.Asp191His Uncertain significance ★★ same residue
BRCA2 p.Asp191= Likely benign ★ 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-asp191ala (accessed [today's date]).

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