Is BRCA2 p.His2623Tyr (c.7867C>T) pathogenic?

BRCA2 p.His2623Tyr (c.7867C>T) is classified Likely pathogenic in BRCA2 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2023-11-30). AlphaMissense: likely pathogenic (0.7968); Absent from gnomAD v4.1; Associated with hereditary breast ovarian cancer syndrome.

What condition is associated with BRCA2 p.His2623Tyr (c.7867C>T)?

BRCA2 p.His2623Tyr (c.7867C>T) is associated with hereditary breast ovarian cancer syndrome, hereditary neoplastic syndrome (ClinVar).

How common is BRCA2 p.His2623Tyr (c.7867C>T) in the general population?

BRCA2 p.His2623Tyr (c.7867C>T) 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.

What do computational predictors say about BRCA2 p.His2623Tyr (c.7867C>T)?

AlphaMissense predicts likely pathogenic (score 0.7968) — an in-silico prediction, not a clinical call.

BRCA2 p.His2623Tyr

c.7867C>T · rs1566244783 · VCV573433

Likely pathogenic Multiple submitters

Classification

Likely pathogenic

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

AlphaMissense

likely pathogenic

0.7968 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

2/2 damaging

AlphaMissense, REVEL

Conditions

hereditary breast ovarian cancer syndrome

Computational evidence

Protein change
AlphaMissense	0.7968	likely pathogenic ✓ concordant with ClinVar · top 3% in BRCA2
REVEL	0.851	moderately pathogenic-leaning
⇒ AlphaMissense and REVEL both call this damaging.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
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	25.7	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

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.His2623Tyr
Coding: c.7867C>T
MANE Select: NM_000059
dbSNP: rs1566244783
Type: single nucleotide variant
Location: chr13:32362584 (GRCh38)
Gene constraint: LOEUF 0.803 · pLI <0.01 · ClinGen HI 3/3 (gnomAD)
Residue 2623: the 'interaction with sem1' region

Full BRCA2 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

Also linked: hereditary neoplastic syndrome

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

Inheritance: Autosomal dominant
Onset: Adult, Elderly

Similar variants

BRCA2 p.His2623Leu Likely pathogenic ★★★ ⚠ same residue
BRCA2 p.His2623Arg Pathogenic/Likely pathogenic ★★ same residue
BRCA2 p.His2623Asn Uncertain significance ★★ ⚠ same residue
BRCA2 p.His2623= Likely benign ★★ same residue
BRCA2 p.His2623Pro Likely pathogenic ★ same residue
BRCA2 p.His2623Asp Uncertain significance ★ ⚠ same residue
BRCA2 c.316+1G>T Pathogenic ★★★ same condition
BRCA2 c.316+2T>C 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-his2623tyr (accessed [today's date]).

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