Is FANCC p.Val239= (c.717A>C) pathogenic?

FANCC p.Val239= (c.717A>C) is classified Likely benign in FANCC (ClinVar, Single submitter, 1 submitter; last evaluated 2025-09-19). Absent from gnomAD v4.1; Associated with hereditary neoplastic syndrome.

What condition is associated with FANCC p.Val239= (c.717A>C)?

FANCC p.Val239= (c.717A>C) is associated with hereditary neoplastic syndrome (ClinVar).

How common is FANCC p.Val239= (c.717A>C) in the general population?

FANCC p.Val239= (c.717A>C) is absent from gnomAD v4.1 (gnomAD).

FANCC p.Val239=

c.717A>C · VCV4641007

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 neoplastic 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 -2.4	GERP -5.6
Overall
CADD	0.703	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: FANCC
Protein: p.Val239=
Coding: c.717A>C
MANE Select: NM_000136
Type: single nucleotide variant
Location: chr9:95135472 (GRCh38)
Gene constraint: LOEUF 1.022 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 82.39 · 6 PDB
Residue 239: an α-helix

Full FANCC 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

FANCC p.Val239Ile Uncertain significance ★★ ⚠ same residue
FANCC c.1073-1G>C Pathogenic/Likely pathogenic ★★ same condition
FANCC c.1155-1G>C Pathogenic/Likely pathogenic ★★ same condition
FANCC c.166-2A>G Pathogenic/Likely pathogenic ★★ same condition
FANCC c.251-2A>C Pathogenic/Likely pathogenic ★★ same condition
FANCC c.345+1G>A Likely pathogenic ★★ same condition
FANCC c.346-1G>A Pathogenic/Likely pathogenic ★★ same condition
FANCC c.456+4A>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/fancc-p-val239 (accessed [today's date]).

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